Lymphatic Endothelial Cells in Health and Disease

Du Tang , Wang Lin , Hengyang Liu , Jixin Zhong , Shiliang Li , Xiaoquan Rao

MedComm ›› 2026, Vol. 7 ›› Issue (8) : e70891

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MedComm ›› 2026, Vol. 7 ›› Issue (8) :e70891 DOI: 10.1002/mco2.70891
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Lymphatic Endothelial Cells in Health and Disease
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Abstract

Lymphatic endothelial cells (LECs) line the lymphatic vasculature and support interstitial fluid drainage, lipid transport, and immune-cell trafficking. Beyond these classical functions, recent studies now recognize LECs as heterogeneous, spatially organized endothelial regulators that maintain lymphatic identity while adopting tissue-, segment-, and disease-associated states. Advances in lineage tracing, multiomics, functional imaging, and perturbation studies now link LEC heterogeneity to drainage control, immune surveillance, antigen handling, metabolic homeostasis, and tissue repair. Despite these advances, a unified framework explaining how developmental origin, tissue niche, and context-dependent state transitions collectively shape LEC function across physiology and disease remains lacking. In this review, we summarize the developmental origins, identity-maintenance mechanisms, and anatomical deployment of LEC states across the lymphatic network. We then discuss how specialized LEC states coordinate lymphatic transport, immune surveillance, and peripheral tolerance under homeostasis. We further examine how context-dependent LEC reprogramming contributes to lymphatic disorders, inflammation and autoimmunity, cancer, cardiometabolic disease, and central nervous system dysfunction. Finally, we highlight challenges and opportunities for translational LEC-targeted therapy. Together, this state-centered framework reframes LECs as actionable regulators of tissue homeostasis and disease progression, providing a conceptual foundation for precision lymphatic medicine.

Keywords

heterogeneity / immune regulation / lymphangiogenesis / lymphatic endothelial cells / lymphatic remodeling / tissue homeostasis

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Du Tang, Wang Lin, Hengyang Liu, Jixin Zhong, Shiliang Li, Xiaoquan Rao. Lymphatic Endothelial Cells in Health and Disease. MedComm, 2026, 7 (8) : e70891 DOI:10.1002/mco2.70891

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References

[1]

L. V. Leak and J. F. Burke, “Fine Structure of the Lymphatic Capillary and the Adjoining Connective Tissue Area,” American Journal of Anatomy 118 (1966): 785–809.

[2]

L. V. Leak and J. F. Burke, “Ultrastructural Studies on the Lymphatic Anchoring Filaments,” Journal of Cell Biology 36 (1968): 129–149.

[3]

G. Oliver and M. Detmar, “The Rediscovery of the Lymphatic System: Old and New Insights Into the Development and Biological Function of the Lymphatic Vasculature,” Genes & Development 16 (2002): 773–783.

[4]

M. S. Pepper and M. Skobe, “Lymphatic Endothelium: Morphological, Molecular and Functional Properties,” Journal of Cell Biology 163 (2003): 209–213.

[5]

R. M. Sheridan, T. A. Doan, C. J. Lucas, et al., “A Specific Gene Expression Program Underlies Antigen Archiving by Lymphatic Endothelial Cells in Mammalian Lymph Nodes,” Nature Communications 16 (2025): 8375.

[6]

E. Sibler, Y. He, L. Ducoli, et al., “Single-Cell Transcriptional Heterogeneity of Lymphatic Endothelial Cells in Normal and Inflamed Murine Lymph Nodes,” Cells 10 (2021): 1371.

[7]

M. J. Davis, S. D. Zawieja, and P. D. King, “Transport and Immune Functions of the Lymphatic System,” Annual Review of Physiology 87 (2025): 151–172.

[8]

Z. Hu, X. Zhao, Z. Wu, et al., “Lymphatic Vessel: Origin, Heterogeneity, Biological Functions, and Therapeutic Targets,” Signal Transduction and Targeted Therapy 9 (2024): 9.

[9]

L. Klotz, S. Norman, J. M. Vieira, et al., “Cardiac Lymphatics Are Heterogeneous in Origin and Respond to Injury,” Nature 522 (2015): 62–67.

[10]

L. Stanczuk, I. Martinez-Corral, M. H. Ulvmar, et al., “cKit Lineage Hemogenic Endothelium-Derived Cells Contribute to Mesenteric Lymphatic Vessels,” Cell Reports 10 (2015): 1708–1721.

[11]

I. Martinez-Corral, M. H. Ulvmar, L. Stanczuk, et al., “Nonvenous Origin of Dermal Lymphatic Vasculature,” Circulation Research 116 (2015): 1649–1654.

[12]

I. E. Lupu, D. E. Grainger, N. Kirschnick, et al., “Direct Specification of Lymphatic Endothelium From Mesenchymal Progenitors,” Nature Cardiovascular Research 4 (2025): 45–63.

[13]

E. Marchaud, R. Morin, J. S. Iacovoni, et al., “3D Imaging and Single-Cell Analysis Reveal Cellular Heterogeneity of Lymphatic Valve Endothelial Cell Types,” iScience 28 (2025): 113841.

[14]

N. Fujimoto, Y. He, M. D'Addio, et al., “Single-Cell Mapping Reveals New Markers and Functions of Lymphatic Endothelial Cells in Lymph Nodes,” PLoS Biology 18 (2020): e3000704.

[15]

A. Takeda, M. Hollmén, D. Dermadi, et al., “Single-Cell Survey of Human Lymphatics Unveils Marked Endothelial Cell Heterogeneity and Mechanisms of Homing for Neutrophils,” Immunity 51 (2019): 561–572.e5.

[16]

E. F. Tewalt, J. N. Cohen, S. J. Rouhani, et al., “Lymphatic Endothelial Cells Induce Tolerance via PD-L1 and Lack of Costimulation Leading to High-Level PD-1 Expression on CD8 T Cells,” Blood 120 (2012): 4772–4782.

[17]

J. N. Cohen, C. J. Guidi, E. F. Tewalt, et al., “Lymph Node-Resident Lymphatic Endothelial Cells Mediate Peripheral Tolerance via Aire-Independent Direct Antigen Presentation,” Journal of Experimental Medicine 207 (2010): 681–688.

[18]

R. C. Ji, “Lymphatic Endothelial Cells and Organ-Associated Lymphangiogenesis in Tumor Microenvironment,” Cells 15 (2025): 28.

[19]

G. Oliver, J. Kipnis, G. J. Randolph, et al., “The Lymphatic Vasculature in the 21(st) Century: Novel Functional Roles in Homeostasis and Disease,” Cell 182 (2020): 270–296.

[20]

M. Sun, J. Angelillo, and S. Hugues, “Lymphatic Transport in Anti-Tumor Immunity and Metastasis,” Journal of Experimental Medicine 222 (2025): e20231954.

[21]

H. Kim, R. P. Kataru, and G. Y. Koh, “Inflammation-Associated Lymphangiogenesis: A Double-Edged Sword?,” Journal of Clinical Investigation 124 (2014): 936–942.

[22]

J. T. Wigle and G. Oliver, “Prox1 Function Is Required for the Development of the Murine Lymphatic System,” Cell 98 (1999): 769–778.

[23]

M. J. Karkkainen, P. Haiko, K. Sainio, et al., “Vascular Endothelial Growth Factor C Is Required for Sprouting of the First Lymphatic Vessels From Embryonic Veins,” Nature Immunology 5 (2004): 74–80.

[24]

R. S. Srinivasan, M. E. Dillard, O. V. Lagutin, et al., “Lineage Tracing Demonstrates the Venous Origin of the Mammalian Lymphatic Vasculature,” Genes & Development 21 (2007): 2422–2432.

[25]

M. François, A. Caprini, B. Hosking, et al., “Sox18 Induces Development of the Lymphatic Vasculature in Mice,” Nature 456 (2008): 643–647.

[26]

R. Hägerling, C. Pollmann, M. Andreas, et al., “A Novel Multistep Mechanism for Initial Lymphangiogenesis in Mouse Embryos Based on Ultramicroscopy,” The EMBO Journal 32 (2013): 629–644.

[27]

S. Yamaguchi, N. Minamide, H. Imai, et al., “The Development of Early Human Lymphatic Vessels as Characterized by Lymphatic Endothelial Markers,” The EMBO Journal 43 (2024): 868–885.

[28]

J. T. Wigle, N. Harvey, M. Detmar, et al., “An Essential Role for Prox1 in the Induction of the Lymphatic Endothelial Cell Phenotype,” The EMBO Journal 21 (2002): 1505–1513.

[29]

R. S. Srinivasan, X. Geng, Y. Yang, et al., “The Nuclear Hormone Receptor Coup-TFII Is Required for the Initiation and Early Maintenance of Prox1 Expression in Lymphatic Endothelial Cells,” Genes & Development 24 (2010): 696–707.

[30]

S. Banerji, J. Ni, S. X. Wang, et al., “LYVE-1, a New Homologue of the CD44 Glycoprotein, Is a Lymph-Specific Receptor for Hyaluronan,” Journal of Cell Biology 144 (1999): 789–801.

[31]

S. Breiteneder-Geleff, A. Soleiman, H. Kowalski, et al., “Angiosarcomas Express Mixed Endothelial Phenotypes of Blood and Lymphatic Capillaries: Podoplanin as a Specific Marker for Lymphatic Endothelium,” American Journal of Pathology 154 (1999): 385–394.

[32]

L. Yuan, D. Moyon, L. Pardanaud, et al., “Abnormal Lymphatic Vessel Development in Neuropilin 2 Mutant Mice,” Development 129 (2002): 4797–4806.

[33]

A. Kaipainen, J. Korhonen, T. Mustonen, et al., “Expression of the Fms-Like Tyrosine Kinase 4 Gene Becomes Restricted to Lymphatic Endothelium During Development,” PNAS 92 (1995): 3566–3570.

[34]

Y. Pan, W. D. Wang, and T. Yago, “Transcriptional Regulation of Podoplanin Expression by Prox1 in Lymphatic Endothelial Cells,” Microvascular Research 94 (2014): 96–102.

[35]

R. S. Srinivasan, N. Escobedo, Y. Yang, et al., “The Prox1-Vegfr3 Feedback Loop Maintains the Identity and the Number of Lymphatic Endothelial Cell Progenitors,” Genes & Development 28 (2014): 2175–2187.

[36]

G. Lioux, X. Liu, S. Temiño, et al., “A Second Heart Field-Derived Vasculogenic Niche Contributes to Cardiac Lymphatics,” Developmental Cell 52 (2020): 350–363.e6.

[37]

K. Maruyama, S. Miyagawa-Tomita, K. Mizukami, et al., “Isl1-Expressing Non-Venous Cell Lineage Contributes to Cardiac Lymphatic Vessel Development,” Developmental Biology 452 (2019): 134–143.

[38]

S. K. Jha, K. Rauniyar, T. Karpanen, et al., “Efficient Activation of the Lymphangiogenic Growth Factor VEGF-C Requires the C-Terminal Domain of VEGF-C and the N-Terminal Domain of CCBE1,” Scientific Reports 7 (2017): 4916.

[39]

M. Osada, O. Inoue, G. Ding, et al., “Platelet Activation Receptor CLEC-2 Regulates Blood/Lymphatic Vessel Separation by Inhibiting Proliferation, Migration, and Tube Formation of Lymphatic Endothelial Cells,” Journal of Biological Chemistry 287 (2012): 22241–22252.

[40]

P. R. Hess, D. R. Rawnsley, Z. Jakus, et al., “Platelets Mediate Lymphovenous Hemostasis to Maintain Blood-Lymphatic Separation Throughout Life,” Journal of Clinical Investigation 124 (2014): 273–284.

[41]

C. C. Bertozzi, A. A. Schmaier, P. Mericko, et al., “Platelets Regulate Lymphatic Vascular Development Through CLEC-2-SLP-76 Signaling,” Blood 116 (2010): 661–670.

[42]

P. Uhrin, J. Zaujec, J. M. Breuss, et al., “Novel Function for Blood Platelets and Podoplanin in Developmental Separation of Blood and Lymphatic Circulation,” Blood 115 (2010): 3997–4005.

[43]

F. Abtahian, A. Guerriero, E. Sebzda, et al., “Regulation of Blood and Lymphatic Vascular Separation by Signaling Proteins SLP-76 and Syk,” Science 299 (2003): 247–251.

[44]

J. Du, P. Liu, Y. Zhou, et al., “The Mechanosensory Channel PIEZO1 Functions Upstream of Angiopoietin/TIE/FOXO1 Signaling in Lymphatic Development,” Journal of Clinical Investigation 134 (2024): e176577.

[45]

T. Mäkinen, R. H. Adams, J. Bailey, et al., “PDZ Interaction Site in ephrinB2 Is Required for the Remodeling of Lymphatic Vasculature,” Genes & Development 19 (2005): 397–410.

[46]

H. S. Baldwin, M. J. Davis, C. Harmelink, et al., “TIE1-Dependent Lymphatic Vascular Remodeling Is Mediated by Its Second Tyrosine Kinase Domain,” Development 152 (2025): dev204469.

[47]

C. Norrmén, K. I. Ivanov, J. Cheng, et al., “FOXC2 Controls Formation and Maturation of Lymphatic Collecting Vessels Through Cooperation With NFATc1,” Journal of Cell Biology 185 (2009): 439–457.

[48]

J. Kazenwadel, K. L. Betterman, C. E. Chong, et al., “GATA2 is Required for Lymphatic Vessel Valve Development and Maintenance,” Journal of Clinical Investigation 125 (2015): 2979–2994.

[49]

E. A. Korhonen, A. Murtomäki, S. K. Jha, et al., “Lymphangiogenesis Requires Ang2/Tie/PI3K Signaling for VEGFR3 Cell-Surface Expression,” Journal of Clinical Investigation 132 (2022): e155478.

[50]

D. T. Sweet, J. M. Jiménez, J. Chang, et al., “Lymph Flow Regulates Collecting Lymphatic Vessel Maturation in Vivo,” Journal of Clinical Investigation 125 (2015): 2995–3007.

[51]

M. J. Davis, S. D. Zawieja, and Y. Yang, “Developmental Progression of Lymphatic Valve Morphology and Function,” Frontiers in Cell and Developmental Biology 12 (2024): 1331291.

[52]

Y. Xu, L. Yuan, J. Mak, et al., “Neuropilin-2 Mediates VEGF-C-Induced Lymphatic Sprouting Together With VEGFR3,” Journal of Cell Biology 188 (2010): 115–130.

[53]

X. Liu, A. Uemura, Y. Fukushima, et al., “Semaphorin 3G Provides a Repulsive Guidance Cue to Lymphatic Endothelial Cells via Neuropilin-2/PlexinD1,” Cell Reports 17 (2016): 2299–2311.

[54]

Y. Uchida, J. M. James, F. Suto, et al., “Class 3 Semaphorins Negatively Regulate Dermal Lymphatic Network Formation,” Biology Open 4 (2015): 1194–1205.

[55]

L. N. H. Do, E. Delgado, C. G. Lim, et al., “A Neuro-Lymphatic Communication Guides Lymphatic Development by CXCL12 and CXCR4 Signaling,” Development 151 (2024): dev202901.

[56]

M. C. Friess, I. Kritikos, P. Schineis, et al., “Mechanosensitive ACKR4 Scavenges CCR7 Chemokines to Facilitate T Cell De-Adhesion and Passive Transport by Flow in Inflamed Afferent Lymphatics,” Cell Reports 38 (2022): 110334.

[57]

J. I. Lane, E. Nieves-Ortiz, O. Ndatabaye, et al., “Intestinal Lymphatic Vasculature Is Functionally Adapted to Different Drainage Regions and Is Altered by Helminth Infection,” Journal of Experimental Medicine 222 (2025): e20241181.

[58]

S. J. Holtkamp, L. M. Ince, C. Barnoud, et al., “Circadian Clocks Guide Dendritic Cells Into Skin Lymphatics,” Nature Immunology 22 (2021): 1375–1381.

[59]

L. Grimm, E. Mason, H. Yu, et al., “Single-Cell Analysis of Lymphatic Endothelial Cell Fate Specification and Differentiation During Zebrafish Development,” The EMBO Journal 42 (2023): e112590.

[60]

W. Ma, H. J. Gil, X. Liu, et al., “Mitochondrial Respiration Controls the Prox1-Vegfr3 Feedback Loop During Lymphatic Endothelial Cell Fate Specification and Maintenance,” Science Advances 7 (2021): eabe7359.

[61]

Y. K. Hong, N. Harvey, Y. H. Noh, et al., “Prox1 is a Master Control Gene in the Program Specifying Lymphatic Endothelial Cell Fate,” Developmental Dynamics 225 (2002): 351–357.

[62]

N. C. Johnson, M. E. Dillard, P. Baluk, et al., “Lymphatic Endothelial Cell Identity Is Reversible and Its Maintenance Requires Prox1 Activity,” Genes & Development 22 (2008): 3282–3291.

[63]

M. J. Yang, S. Kang, S. P. Hong, et al., “Cooperative ETS Transcription Factors Are Required for Lymphatic Endothelial Cell Integrity and Resilience,” Journal of Clinical Investigation 136 (2026): e196119.

[64]

G. J. Randolph, S. Ivanov, B. H. Zinselmeyer, et al., “The Lymphatic System: Integral Roles in Immunity,” Annual Review of Immunology 35 (2017): 31–52.

[65]

S. Podgrabinska, P. Braun, P. Velasco, et al., “Molecular Characterization of Lymphatic Endothelial Cells,” PNAS 99 (2002): 16069–16074.

[66]

S. Jalkanen and M. Salmi, “Lymphatic Endothelial Cells of the Lymph Node,” Nature Reviews Immunology 20 (2020): 566–578.

[67]

S. J. Berendam, A. F. Koeppel, N. R. Godfrey, et al., “Comparative Transcriptomic Analysis Identifies a Range of Immunologically Related Functional Elaborations of Lymph Node Associated Lymphatic and Blood Endothelial Cells,” Frontiers in Immunology 10 (2019): 816.

[68]

R. Z. Niu, H. Y. Xu, H. Tian, et al., “Single-Cell Transcriptome Unveils Unique Transcriptomic Signatures of Human Organ-Specific Endothelial Cells,” Basic Research in Cardiology 119 (2024): 973–999.

[69]

S. N. Barnett, A. M. Cujba, L. Yang, et al., “An Organotypic Atlas of Human Vascular Cells,” Nature Medicine 30 (2024): 3468–3481.

[70]

J. Kalucka, L. de Rooij, J. Goveia, et al., “Single-Cell Transcriptome Atlas of Murine Endothelial Cells,” Cell 180 (2020): 764–779.e20.

[71]

S. I. Travisano, M. R. M. Harrison, M. E. Thornton, et al., “Single-Nuclei Multiomic Analyses Identify Human Cardiac Lymphatic Endothelial Cells Associated With Coronary Arteries in the Epicardium,” Cell Reports 42 (2023): 113106.

[72]

I. L. Grigorova, M. Panteleev, and J. G. Cyster, “Lymph Node Cortical Sinus Organization and Relationship to Lymphocyte Egress Dynamics and Antigen Exposure,” PNAS 107 (2010): 20447–20452.

[73]

C. R. Bastow, M. D. Bunting, E. E. Kara, et al., “Scavenging of Soluble and Immobilized CCL21 by ACKR4 Regulates Peripheral Dendritic Cell Emigration,” PNAS 118 (2021): e2025763118.

[74]

S. A. Bryce, R. A. Wilson, E. M. Tiplady, et al., “ACKR4 on Stromal Cells Scavenges CCL19 To Enable CCR7-Dependent Trafficking of APCs From Inflamed Skin to Lymph Nodes,” Journal of Immunology 196 (2016): 3341–3353.

[75]

M. H. Ulvmar, K. Werth, A. Braun, et al., “The Atypical Chemokine Receptor CCRL1 Shapes Functional CCL21 Gradients in Lymph Nodes,” Nature Immunology 15 (2014): 623–630.

[76]

R. M. Kedl, R. S. Lindsay, J. M. Finlon, et al., “Migratory Dendritic Cells Acquire and Present Lymphatic Endothelial Cell-Archived Antigens During Lymph Node Contraction,” Nature Communications 8 (2017): 2034.

[77]

B. A. Tamburini, M. A. Burchill, and R. M. Kedl, “Antigen Capture and Archiving by Lymphatic Endothelial Cells Following Vaccination or Viral Infection,” Nature Communications 5 (2014): 3989.

[78]

A. González-Loyola, E. Bovay, J. Kim, et al., “FOXC2 Controls Adult Lymphatic Endothelial Specialization, Function, and Gut Lymphatic Barrier Preventing Multiorgan Failure,” Science Advances 7 (2021): eabf4335.

[79]

M. Ma, L. Li, S. H. Yang, et al., “Lymphatic Endothelial Cell-Mediated Accumulation of CD177(+)Treg Cells Suppresses Antitumor Immunity in Human Esophageal Squamous Cell Carcinoma,” Oncoimmunology 13 (2024): 2327692.

[80]

A. Braun, T. Worbs, G. L. Moschovakis, et al., “Afferent Lymph-Derived T Cells and DCs Use Different Chemokine Receptor CCR7-Dependent Routes for Entry Into the Lymph Node and Intranodal Migration,” Nature Immunology 12 (2011): 879–887.

[81]

S. M. Walsh, R. M. Sheridan, E. D. Lucas, et al., “Molecular Tracking Devices Quantify Antigen Distribution and Archiving in the Murine Lymph Node,” Elife 10 (2021): e62781.

[82]

L. A. Johnson, S. Banerji, W. Lawrance, et al., “Dendritic Cells Enter Lymph Vessels by Hyaluronan-Mediated Docking to the Endothelial Receptor LYVE-1,” Nature Immunology 18 (2017): 762–770.

[83]

H. Pflicke and M. Sixt, “Preformed Portals Facilitate Dendritic Cell Entry Into Afferent Lymphatic Vessels,” Journal of Experimental Medicine 206 (2009): 2925–2935.

[84]

M. Jannaway, D. Iyer, D. M. Mastrogiacomo, et al., “VEGFR3 is Required for Button Junction Formation in Lymphatic Vessels,” Cell Reports 42 (2023): 112777.

[85]

P. Baluk, J. Fuxe, H. Hashizume, et al., “Functionally Specialized Junctions Between Endothelial Cells of Lymphatic Vessels,” Journal of Experimental Medicine 204 (2007): 2349–2362.

[86]

M. J. Churchill, H. du Bois, T. A. Heim, et al., “Infection-Induced Lymphatic Zippering Restricts Fluid Transport and Viral Dissemination From Skin,” Journal of Experimental Medicine 219 (2022): e20211830.

[87]

F. Zhang, G. Zarkada, J. Han, et al., “Lacteal Junction Zippering Protects Against Diet-Induced Obesity,” Science 361 (2018): 599–603.

[88]

J. Bernier-Latmani, C. Cisarovsky, C. S. Demir, et al., “DLL4 Promotes Continuous Adult Intestinal Lacteal Regeneration and Dietary Fat Transport,” Journal of Clinical Investigation 125 (2015): 4572–4586.

[89]

G. Zarkada, X. Chen, X. Zhou, et al., “Chylomicrons Regulate Lacteal Permeability and Intestinal Lipid Absorption,” Circulation Research 133 (2023): 333–349.

[90]

W. Wang, X. Li, X. Ding, et al., “Lymphatic Endothelial Transcription Factor Tbx1 Promotes an Immunosuppressive Microenvironment to Facilitate Post-Myocardial Infarction Repair,” Immunity 56 (2023): 2342–2357.e10.

[91]

J. M. Vieira, S. Norman, C. Villa Del Campo, et al., “The Cardiac Lymphatic System Stimulates Resolution of Inflammation Following Myocardial Infarction,” Journal of Clinical Investigation 128 (2018): 3402–3412.

[92]

J. He, D. Zhang, H. Song, et al., “Single-Cell and Spatial Transcriptomic Analyses Reveals the Dynamic Transcript Profiles of Myocardial Lymphangiogenesis Post-Myocardial Infarction,” Elife 13 (2024): RP99192.

[93]

T. K. Patel, L. Habimana-Griffin, X. Gao, et al., “Dural Lymphatics Regulate Clearance of Extracellular Tau From the CNS,” Molecular Neurodegeneration 14 (2019): 11.

[94]

A. Louveau, J. Herz, M. N. Alme, et al., “CNS Lymphatic Drainage and Neuroinflammation Are Regulated by Meningeal Lymphatic Vasculature,” Nature Neuroscience 21 (2018): 1380–1391.

[95]

S. P. das Neves, N. Delivanoglou, Y. Ren, et al., “Meningeal Lymphatic Function Promotes Oligodendrocyte Survival and Brain Myelination,” Immunity 57 (2024): 2328–2343.e8.

[96]

A. Louveau, I. Smirnov, T. J. Keyes, et al., “Structural and Functional Features of Central Nervous System Lymphatic Vessels,” Nature 523 (2015): 337–341.

[97]

A. O. Gkountidi, L. Garnier, J. Dubrot, et al., “MHC Class II Antigen Presentation by Lymphatic Endothelial Cells in Tumors Promotes Intratumoral Regulatory T Cell-Suppressive Functions,” Cancer Immunology Research 9 (2021): 748–764.

[98]

N. Cousin, S. Cap, M. Dihr, et al., “Lymphatic PD-L1 Expression Restricts Tumor-Specific CD8(+) T-Cell Responses,” Cancer Research 81 (2021): 4133–4144.

[99]

L. C. Dieterich, K. Ikenberg, T. Cetintas, et al., “Tumor-Associated Lymphatic Vessels Upregulate PDL1 to Inhibit T-Cell Activation,” Frontiers in Immunology 8 (2017): 66.

[100]

B. W. Wong, X. Wang, A. Zecchin, et al., “The Role of Fatty Acid β-Oxidation in Lymphangiogenesis,” Nature 542 (2017): 49–54.

[101]

O. Meçe, D. Houbaert, M. L. Sassano, et al., “Lipid Droplet Degradation by Autophagy Connects Mitochondria Metabolism to Prox1-Driven Expression of Lymphatic Genes and Lymphangiogenesis,” Nature Communications 13 (2022): 2760.

[102]

J. D. Kim, S. Chaudhary, W. Chen, et al., “APOA1 Binding Protein Promotes Lymphatic Cell Fate and Lymphangiogenesis by Relieving Caveolae-Mediated Inhibition of VEGFR3 Signaling,” Nature Communications 16 (2025): 9286.

[103]

Y. Kondo, Y. Jiang, X. Geng, et al., “Site-1 Protease-Mediated Cholesterol Metabolism Is Essential for Lymphatic Development in Mice,” JCI Insight 10 (2025): e188637.

[104]

K. C. Rajan, N. R. Patel, A. Shenoy, et al., “Zmiz1 is a Novel Regulator of Lymphatic Endothelial Cell Gene Expression and Function,” PLoS One 19 (2024): e0302926.

[105]

V. Panara, H. Yu, D. Peng, et al., “Multiple Cis-Regulatory Elements Control prox1a Expression in Distinct Lymphatic Vascular Beds,” Development 151 (2024): dev202269.

[106]

N. Laugero, C. Peghaire, L. Verdu, et al., “lncRNA LINC-PINT Controls Lymphatic Function and Inflammatory Profile in Lymphedema,” Science Advances 11 (2025): eaea2960.

[107]

D. Houbaert, A. P. Nikolakopoulos, K. A. Jacobs, et al., “An Autophagy Program That Promotes T Cell Egress From the Lymph Node Controls Responses to Immune Checkpoint Blockade,” Cell Reports 43 (2024): 114020.

[108]

S. Brönneke, B. Brückner, N. Peters, et al., “DNA Methylation Regulates Lineage-Specifying Genes in Primary Lymphatic and Blood Endothelial Cells,” Angiogenesis 15 (2012): 317–329.

[109]

C. Tacconi, Y. He, L. Ducoli, et al., “Epigenetic Regulation of the Lineage Specificity of Primary Human Dermal Lymphatic and Blood Vascular Endothelial Cells,” Angiogenesis 24 (2021): 67–82.

[110]

S. Durot, P. F. Doubleday, L. Schulla, et al., “Multi-Omics Analysis Reveals Metabolic Diversity Underlying Endothelial Cell Functions,” Life Science Alliance 9 (2026): e202503526.

[111]

L. C. Yao, P. Baluk, R. S. Srinivasan, et al., “Plasticity of Button-Like Junctions in the Endothelium of Airway Lymphatics in Development and Inflammation,” American Journal of Pathology 180 (2012): 2561–2575.

[112]

E. Weber, A. Rossi, R. Solito, et al., “Focal Adhesion Molecules Expression and Fibrillin Deposition by Lymphatic and Blood Vessel Endothelial Cells in Culture,” Microvascular Research 64 (2002): 47–55.

[113]

R. Gerli, R. Solito, E. Weber, et al., “Specific Adhesion Molecules Bind Anchoring Filaments and Endothelial Cells in Human Skin Initial Lymphatics,” Lymphology 33 (2000): 148–157.

[114]

J. R. Casley-Smith, “Are the Initial Lymphatics Normally Pulled Open by the Anchoring Filaments?,” Lymphology 13 (1980): 120–129.

[115]

Y. Wang, Y. Jin, M. A. Mäe, et al., “Smooth Muscle Cell Recruitment to Lymphatic Vessels Requires PDGFB and Impacts Vessel Size but Not Identity,” Development 144 (2017): 3590–3601.

[116]

S. Ohgaku, S. Ida, N. Ohashi, et al., “O-GlcNAc Modification in Endothelial Cells Modulates Adiposity via Fat Absorption From the Intestine in Mice,” Heliyon 10 (2024): e34490.

[117]

M. Sáinz-Jaspeado, S. Ring, S. T. Proulx, et al., “VE-Cadherin Junction Dynamics in Initial Lymphatic Vessels Promotes Lymph Node Metastasis,” Life Science Alliance 7 (2024): e202302168.

[118]

P. R. Norden and T. Kume, “Molecular Mechanisms Controlling Lymphatic Endothelial Junction Integrity,” Frontiers in Cell and Developmental Biology 8 (2020): 627647.

[119]

E. Solari, C. Marcozzi, D. Negrini, et al., “The “Useful” Hindrance to Flow: Quantification of Intraluminal Valves Effect on Lymph Flow Driven by Intrinsic Mechanism in the Diaphragmatic Lymphatic Network,” American Journal of Physiology. Heart and Circulatory Physiology 330 (2026): H388–H403.

[120]

M. J. Davis and C. D. Bertram, “Control of Lymphatic Pacemaking and Pumping by Mechanobiological Signals,” Journal De Physiologie 603 (2025): 3307–3327.

[121]

S. D. Zawieja, G. A. Pea, S. E. Broyhill, et al., “Cellular Characterization of the Mouse Collecting Lymphatic Vessels Reveals That Lymphatic Muscle Cells Are the Innate Pacemaker Cells,” Elife 12 (2025): RP90679.

[122]

M. J. Davis, E. Rahbar, A. A. Gashev, et al., “Determinants of Valve Gating in Collecting Lymphatic Vessels From Rat Mesentery,” American Journal of Physiology. Heart and Circulatory Physiology 301 (2011): H48–60.

[123]

N. Wick, D. Haluza, E. Gurnhofer, et al., “Lymphatic Precollectors Contain a Novel, Specialized Subpopulation of Podoplanin Low, CCL27-Expressing Lymphatic Endothelial Cells,” American Journal of Pathology 173 (2008): 1202–1209.

[124]

M. Albayram, S. B. Richmond, K. Yagmurlu, et al., “Meningeal Lymphatic Architecture and Drainage Dynamics Surrounding the Human Middle Meningeal Artery,” iScience 28 (2025): 113693.

[125]

Z. Papadopoulos, L. C. D. Smyth, I. Smirnov, et al., “Differential Impact of Lymphatic Outflow Pathways on Cerebrospinal Fluid Homeostasis,” Journal of Experimental Medicine 222 (2025): e20241752.

[126]

D. J. Jafree, B. J. Stewart, K. L. Price, et al., “Organ-Specific Features of Human Kidney Lymphatics Are Disrupted in Chronic Transplant Rejection,” Journal of Clinical Investigation 135 (2025): e168962.

[127]

J. H. Yoon, H. Jin, H. J. Kim, et al., “Nasopharyngeal Lymphatic Plexus Is a Hub for Cerebrospinal Fluid Drainage,” Nature 625 (2024): 768–777.

[128]

S. Stritt, K. Koltowska, and T. Mäkinen, “Homeostatic Maintenance of the Lymphatic Vasculature,” Trends in Molecular Medicine 27 (2021): 955–970.

[129]

N. Itai, E. Gantumur, K. Tsujita-Inoue, et al., “Lymphangiogenesis and Lymphatic Zippering in Skin Associated With the Progression of Lymphedema,” Journal of Investigative Dermatology 144 (2024): 659–668.e7.

[130]

L. A. Johnson, S. Banerji, B. C. Lagerholm, et al., “Dendritic Cell Entry to Lymphatic Capillaries Is Orchestrated by CD44 and the Hyaluronan Glycocalyx,” Life Science Alliance 4 (2021): e202000908.

[131]

F. Bano, S. Banerji, T. Ni, et al., “Structure and Unusual Binding Mechanism of the Hyaluronan Receptor LYVE-1 Mediating Leucocyte Entry to Lymphatics,” Nature Communications 16 (2025): 2754.

[132]

J. W. Breslin, “Mechanical Forces and Lymphatic Transport,” Microvascular Research 96 (2014): 46–54.

[133]

V. Cifarelli and A. Eichmann, “The Intestinal Lymphatic System: Functions and Metabolic Implications,” Cellular and Molecular Gastroenterology & Hepatology 7 (2019): 503–513.

[134]

K. Choe, J. Y. Jang, I. Park, et al., “Intravital Imaging of Intestinal Lacteals Unveils Lipid Drainage Through Contractility,” Journal of Clinical Investigation 125 (2015): 4042–4052.

[135]

M. M. Syed-Abdul, L. Tian, T. Samuel, et al., “Glucagon-Like-Peptide-2 Stimulates Lacteal Contractility and Enhances Chylomicron Transport in the Presence of an Intact Enteric Nervous System,” Gastro Hep Advances 3 (2024): 954–964.

[136]

L. Tian, M. M. Syed-Abdul, and G. F. Lewis, “Activation of VEGFR3 and MLC2 Are Critical for GLP-2 Enhancement of Chylomicron Transport,” Gastro Hep Advances 4 (2025): 100605.

[137]

S. H. Suh, K. Choe, S. P. Hong, et al., “Gut Microbiota Regulates Lacteal Integrity by Inducing VEGF-C in Intestinal Villus Macrophages,” EMBO Reports 20 (2019): e46927.

[138]

S. P. Hong, M. J. Yang, H. Cho, et al., “Distinct Fibroblast Subsets Regulate Lacteal Integrity Through YAP/TAZ-Induced VEGF-C in Intestinal Villi,” Nature Communications 11 (2020): 4102.

[139]

H. Y. Lim, C. H. Thiam, K. P. Yeo, et al., “Lymphatic Vessels Are Essential for the Removal of Cholesterol From Peripheral Tissues by SR-BI-Mediated Transport of HDL,” Cell Metabolism 17 (2013): 671–684.

[140]

C. Martel, W. Li, B. Fulp, et al., “Lymphatic Vasculature Mediates Macrophage Reverse Cholesterol Transport in Mice,” Journal of Clinical Investigation 123 (2013): 1571–1579.

[141]

Y. Y. Zhao, Y. F. Li, J. W. Hao, et al., “DHHC5 Regulates Lacteal Function and Intestinal Lipid Absorption by Maintaining VEGFR2 Localization in Lipid Rafts,” Life Metabolism 4 (2025): loaf014.

[142]

S. J. Rouhani, J. D. Eccles, P. Riccardi, et al., “Roles of Lymphatic Endothelial Cells Expressing Peripheral Tissue Antigens in CD4 T-Cell Tolerance Induction,” Nature Communications 6 (2015): 6771.

[143]

S. Tadayon, J. Dunkel, A. Takeda, et al., “Lymphatic Endothelial Cell Activation and Dendritic Cell Transmigration Is Modified by Genetic Deletion of Clever-1,” Frontiers in Immunology 12 (2021): 602122.

[144]

O. Tal, H. Y. Lim, I. Gurevich, et al., “DC Mobilization From the Skin Requires Docking to Immobilized CCL21 on Lymphatic Endothelium and Intralymphatic Crawling,” Journal of Experimental Medicine 208 (2011): 2141–2153.

[145]

I. Liaqat, I. Hilska, M. Saario, et al., “Spatially Targeted Chemokine Exocytosis Guides Transmigration at Lymphatic Endothelial Multicellular Junctions,” The EMBO Journal 43 (2024): 3141–3174.

[146]

E. Russo, A. Teijeira, K. Vaahtomeri, et al., “Intralymphatic CCL21 Promotes Tissue Egress of Dendritic Cells Through Afferent Lymphatic Vessels,” Cell Reports 14 (2016): 1723–1734.

[147]

V. Collado-Diaz, M. N. Christakopoulou, P. Schineis, et al., “uPA-Mediated Remodeling of CCL21 Gradients Regulates Lymphatic Migration of Dendritic Cells,” Journal of Cell Biology 225 (2026): e202412190.

[148]

L. A. Johnson, S. Clasper, A. P. Holt, et al., “An Inflammation-Induced Mechanism for Leukocyte Transmigration Across Lymphatic Vessel Endothelium,” Journal of Experimental Medicine 203 (2006): 2763–2777.

[149]

J. Arasa, V. Collado-Diaz, I. Kritikos, et al., “Upregulation of VCAM-1 in Lymphatic Collectors Supports Dendritic Cell Entry and Rapid Migration to Lymph Nodes in Inflammation,” Journal of Experimental Medicine 218 (2021): e20201413.

[150]

S. Podgrabinska, O. Kamalu, L. Mayer, et al., “Inflamed Lymphatic Endothelium Suppresses Dendritic Cell Maturation and Function via Mac-1/ICAM-1-Dependent Mechanism,” Journal of Immunology 183 (2009): 1767–1779.

[151]

M. Matloubian, C. G. Lo, G. Cinamon, et al., “Lymphocyte Egress From Thymus and Peripheral Lymphoid Organs Is Dependent on S1P Receptor 1,” Nature 427 (2004): 355–360.

[152]

A. Mendoza, B. Bréart, W. D. Ramos-Perez, et al., “The Transporter Spns2 Is Required for Secretion of Lymph but Not Plasma Sphingosine-1-Phosphate,” Cell Reports 2 (2012): 1104–1110.

[153]

S. Fukuhara, S. Simmons, S. Kawamura, et al., “The Sphingosine-1-Phosphate Transporter Spns2 Expressed on Endothelial Cells Regulates Lymphocyte Trafficking in Mice,” Journal of Clinical Investigation 122 (2012): 1416–1426.

[154]

V. Fang, V. S. Chaluvadi, W. D. Ramos-Perez, et al., “Gradients of the Signaling Lipid S1P in Lymph Nodes Position Natural Killer Cells and Regulate Their Interferon-γ Response,” Nature Immunology 18 (2017): 15–25.

[155]

A. Mendoza, V. Fang, C. Chen, et al., “Lymphatic Endothelial S1P Promotes Mitochondrial Function and Survival in Naive T Cells,” Nature 546 (2017): 158–161.

[156]

I. L. Grigorova, S. R. Schwab, T. G. Phan, et al., “Cortical Sinus Probing, S1P1-Dependent Entry and Flow-Based Capture of Egressing T Cells,” Nature Immunology 10 (2009): 58–65.

[157]

W. Piao, L. Li, V. Saxena, et al., “PD-L1 Signaling Selectively Regulates T Cell Lymphatic Transendothelial Migration,” Nature Communications 13 (2022): 2176.

[158]

M. Sixt, N. Kanazawa, M. Selg, et al., “The Conduit System Transports Soluble Antigens From the Afferent Lymph to Resident Dendritic Cells in the T Cell Area of the Lymph Node,” Immunity 22 (2005): 19–29.

[159]

J. E. Gretz, C. C. Norbury, A. O. Anderson, et al., “Lymph-Borne Chemokines and Other Low Molecular Weight Molecules Reach High Endothelial Venules via Specialized Conduits While a Functional Barrier Limits Access to the Lymphocyte Microenvironments in Lymph Node Cortex,” Journal of Experimental Medicine 192 (2000): 1425–1440.

[160]

R. Roozendaal, T. R. Mempel, L. A. Pitcher, et al., “Conduits Mediate Transport of Low-Molecular-Weight Antigen to Lymph Node Follicles,” Immunity 30 (2009): 264–276.

[161]

Y. R. Carrasco and F. D. Batista, “B Cells Acquire Particulate Antigen in a Macrophage-Rich Area at the Boundary Between the Follicle and the Subcapsular Sinus of the Lymph Node,” Immunity 27 (2007): 160–171.

[162]

T. Junt, E. A. Moseman, M. Iannacone, et al., “Subcapsular Sinus Macrophages in Lymph Nodes Clear Lymph-Borne Viruses and Present Them to Antiviral B Cells,” Nature 450 (2007): 110–114.

[163]

T. G. Phan, J. A. Green, E. E. Gray, et al., “Immune Complex Relay by Subcapsular Sinus Macrophages and Noncognate B Cells Drives Antibody Affinity Maturation,” Nature Immunology 10 (2009): 786–793.

[164]

T. A. Doan, T. S. Forward, J. B. Schafer, et al., “Immunization-Induced Antigen Archiving Enhances Local Memory CD8+ T Cell Responses Following an Unrelated Viral Infection,” NPJ Vaccines 9 (2024): 66.

[165]

Q. Huang, X. Wu, Z. Wang, et al., “The Primordial Differentiation of Tumor-Specific Memory CD8(+) T Cells as Bona Fide Responders to PD-1/PD-L1 Blockade in Draining Lymph Nodes,” Cell 185 (2022): 4049–4066.e25.

[166]

R. Mezyk-Kopec, L. Potin, J. E. Gomez Medellin, et al., “TGF-β Signaling Prevents MHC Class II-Expressing Lymphatic Endothelial Cells From Reactivating Human Allogenic Memory CD4+ T Cells,” Journal of Immunology 211 (2023): 782–790.

[167]

J. Dubrot, F. V. Duraes, L. Potin, et al., “Lymph Node Stromal Cells Acquire Peptide-MHCII Complexes From Dendritic Cells and Induce Antigen-Specific CD4+ T Cell Tolerance,” Journal of Experimental Medicine 211 (2014): 1153–1166.

[168]

M. Nörder, M. G. Gutierrez, S. Zicari, et al., “Lymph Node-Derived Lymphatic Endothelial Cells Express Functional Costimulatory Molecules and Impair Dendritic Cell-Induced Allogenic T-Cell Proliferation,” The FASEB Journal 26 (2012): 2835–2846.

[169]

E. Vokali, S. S. Yu, S. Hirosue, et al., “Lymphatic Endothelial Cells Prime Naïve CD8(+) T Cells Into Memory Cells Under Steady-State Conditions,” Nature Communications 11 (2020): 538.

[170]

M. Okuniewska, V. Fang, A. Baeyens, et al., “SPNS2 Enables T Cell Egress From Lymph Nodes During an Immune Response,” Cell Reports 36 (2021): 109368.

[171]

C. J. Lucas, R. M. Sheridan, G. V. Reynoso, et al., “Chikungunya Virus Infection Disrupts Lymph Node Lymphatic Endothelial Cell Composition and Function via MARCO,” JCI Insight 9 (2024): e176537.

[172]

E. Martini, “Lymphatic Endothelial Cells Orchestrate Cardiac Immunotolerance After Myocardial Infarction,” Nature Cardiovascular Research 2 (2023): 960.

[173]

A. J. Seibel, C. L. Frosti, A. R. Tlemçani, et al., “Obesity-Associated Conditions Hinder Solute Drainage Function of Engineered Human Lymphatic Vessels,” Cellular and Molecular Bioengineering 18 (2025): 53–69.

[174]

X. Guo, C. Huang, L. Zhang, et al., “Lymphatic Endothelial Branched-Chain Amino Acid Catabolic Defects Undermine Cardiac Lymphatic Integrity and Drive HFpEF,” Circulation 151 (2025): 1651–1666.

[175]

D. Szőke, G. Kovács, É. Kemecsei, et al., “Nucleoside-Modified VEGFC mRNA Induces Organ-Specific Lymphatic Growth and Reverses Experimental Lymphedema,” Nature Communications 12 (2021): 3460.

[176]

J. Creff, A. Lamaa, E. Benuzzi, et al., “Apelin-VEGF-C mRNA Delivery as Therapeutic for the Treatment of Secondary Lymphedema,” EMBO Molecular Medicine 16 (2024): 386–415.

[177]

T. Yamashita, U. Kaplan, A. Chakraborty, et al., “ERG Regulates Lymphatic Vessel Specification Genes and Its Deficiency Impairs Wound Healing-Associated Lymphangiogenesis,” Arthritis & Rheumatology 76 (2024): 1645–1657.

[178]

S. Kim, Y. Lee, J. Y. Kwon, et al., “Immune Regulation and Lymphangiogenesis by Lymphatic Endothelial Cells in the Decidua in Severe Preeclampsia,” Scientific Reports 16 (2026): 5181.

[179]

C. Qiu, C. Tang, Y. Tang, et al., “RGS5(+) Lymphatic Endothelial Cells Facilitate Metastasis and Acquired Drug Resistance of Breast Cancer Through Oxidative Stress-Sensing Mechanism,” Drug Resistance Updates 77 (2024): 101149.

[180]

Q. Shen, G. Gu, D. Yang, et al., “Dysfunction and Pathological Origins of Lymphatic Endothelial Cells in Atherosclerosis Revealed by Single-Cell Transcriptomics,” Genes (Basel) 16 (2025): 1398.

[181]

C. Heron, T. Lemarcis, O. Laguerre, et al., “Molecular Determinants of Cardiac Lymphatic Dysfunction in a Chronic Pressure-Overload Model,” EMBO Molecular Medicine 18 (2026): 325–355.

[182]

P. Brouillard, A. Murtomäki, V. M. Leppänen, et al., “Loss-of-Function Mutations of the TIE1 Receptor Tyrosine Kinase Cause Late-Onset Primary Lymphedema,” Journal of Clinical Investigation 134 (2024): e173586.

[183]

T. V. Petrova, T. Karpanen, C. Norrmén, et al., “Defective Valves and Abnormal Mural Cell Recruitment Underlie Lymphatic Vascular Failure in Lymphedema Distichiasis,” Nature Medicine 10 (2004): 974–981.

[184]

A. Irrthum, M. J. Karkkainen, K. Devriendt, et al., “Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase,” American Journal of Human Genetics 67 (2000): 295–301.

[185]

M. J. Karkkainen, R. E. Ferrell, E. C. Lawrence, et al., “Missense Mutations Interfere With VEGFR-3 Signalling in Primary Lymphoedema,” Nature Genetics 25 (2000): 153–159.

[186]

J. C. Zampell, A. Yan, S. Elhadad, et al., “CD4(+) Cells Regulate Fibrosis and Lymphangiogenesis in Response to Lymphatic Fluid Stasis,” PLoS One 7 (2012): e49940.

[187]

M. J. Weiler, M. T. Cribb, Z. Nepiyushchikh, et al., “A Novel Mouse Tail Lymphedema Model for Observing Lymphatic Pump Failure During Lymphedema Development,” Scientific Reports 9 (2019): 10405.

[188]

H. J. Park, J. Shin, A. Sarker, et al., “TGF-β-Mediated Epithelial-Mesenchymal Transition of Keratinocytes Promotes Fibrosis in Secondary Lymphedema,” JCI Insight 10 (2025): e192890.

[189]

G. D. García Nores, C. L. Ly, D. A. Cuzzone, et al., “CD4(+) T Cells Are Activated in Regional Lymph Nodes and Migrate to Skin to Initiate Lymphedema,” Nature Communications 9 (2018): 1970.

[190]

A. C. Campbell, A. R. Stull-Lane, J. E. Baik, et al., “Lymphedema Pathogenesis Involves Antigen-Driven Expansion of CD4+ T Cells in Skin,” Frontiers in Immunology 16 (2025): 1620571.

[191]

J. E. Baik, H. J. Park, R. P. Kataru, et al., “TGF-β1 Mediates Pathologic Changes of Secondary Lymphedema by Promoting Fibrosis and Inflammation,” Clinical and Translational Medicine 12 (2022): e758.

[192]

A. J. Christiansen, L. C. Dieterich, I. Ohs, et al., “Lymphatic Endothelial Cells Attenuate Inflammation via Suppression of Dendritic Cell Maturation,” Oncotarget 7 (2016): 39421–39435.

[193]

L. A. Johnson and D. G. Jackson, “Inflammation-Induced Secretion of CCL21 in Lymphatic Endothelium Is a Key Regulator of Integrin-Mediated Dendritic Cell Transmigration,” International Immunology 22 (2010): 839–849.

[194]

C. Y. Li, H. J. Park, J. Shin, et al., “Tumor-Associated Lymphatics Upregulate MHC-II to Suppress Tumor-Infiltrating Lymphocytes,” International Journal of Molecular Sciences 23 (2022): 13470.

[195]

B. S. Lee, J. Y. Jang, C. Seo, et al., “Crosstalk Between Head and Neck Cancer Cells and Lymphatic Endothelial Cells Promotes Tumor Metastasis via CXCL5-CXCR2 Signaling,” The FASEB Journal 35 (2021): e21181.

[196]

J. Lin, A. S. Lalani, T. C. Harding, et al., “Inhibition of Lymphogenous Metastasis Using Adeno-Associated Virus-Mediated Gene Transfer of a Soluble VEGFR-3 Decoy Receptor,” Cancer Research 65 (2005): 6901–6909.

[197]

Q. Li, C. Zhou, K. Zhao, et al., “Lymphatic Endothelial Sphingosine 1-Phosphate Receptor 1 Enhances Macrophage Clearance via Lymphatic System Following Myocardial Infarction,” Frontiers in Cardiovascular Medicine 9 (2022): 872102.

[198]

A. Milasan, A. Smaani, and C. Martel, “Early Rescue of Lymphatic Function Limits Atherosclerosis Progression in Ldlr(-/-) Mice,” Atherosclerosis 283 (2019): 106–119.

[199]

C. Silvestre-Roig, P. Lemnitzer, J. Gall, et al., “Arterial Delivery of VEGF-C Stabilizes Atherosclerotic Lesions,” Circulation Research 128 (2021): 284–286.

[200]

L. Vachon, A. Smaani, N. Tessier, et al., “Downregulation of Low-Density Lipoprotein Receptor mRNA in Lymphatic Endothelial Cells Impairs Lymphatic Function Through Changes in Intracellular Lipids,” Theranostics 12 (2022): 1440–1458.

[201]

M. Carrillo Diaz de Leon, K. Keane, S. Roizes, et al., “Not Just Fibrotic: Endothelial-Derived TGFβ Maintains Contractile Function and Lymphatic Muscle Phenotype During Homeostasis,” American Journal of Physiology-Cell Physiology 326 (2024): C269–C281.

[202]

D. Choi, E. Park, J. Choi, et al., “Piezo1 Regulates Meningeal Lymphatic Vessel Drainage and Alleviates Excessive CSF Accumulation,” Nature Neuroscience 27 (2024): 913–926.

[203]

N. Morooka, N. Gui, K. Ando, et al., “Angpt1 Binding to Tie1 Regulates the Signaling Required for Lymphatic Vessel Development in Zebrafish,” Development 151 (2024): dev202269.

[204]

A. C. Campbell, J. E. Baik, A. Sarker, et al., “Breast Cancer-Related Lymphedema Results in Impaired Epidermal Differentiation and Tight Junction Dysfunction,” Journal of Investigative Dermatology 145 (2025): 85–97.e4.

[205]

M. J. Ludlow, O. V. Povstyan, D. M. Linley, et al., “PIEZO1 Mechanical Insensitivity in Generalized Lymphatic Dysplasia With the Potential for Pharmacological Rescue,” Iscience 28 (2025): 113110.

[206]

Y. V. Filina, M. A. Zolotykh, and R. R. Miftakhova, “Decreased Kinase Activity of the VEGFR3 Variant c.3175G>C Associated With Primary Lymphedema,” Current Issues in Molecular Biology 48 (2026): 68.

[207]

E. Michalaki, K. Jeong, R. Chin, et al., “Lipid Nanoparticle Library Screen Reveals Lymphatic Endothelial Cell-Targeting Lipid Nanoparticle for Delivering Vascular Endothelial Growth Factor C mRNA After Lymphatic Injury,” ACS Nano 19 (2025): 40873–40891.

[208]

A. Saaristo, T. Veikkola, B. Enholm, et al., “Adenoviral VEGF-C Overexpression Induces Blood Vessel Enlargement, Tortuosity, and Leakiness but no Sprouting Angiogenesis in the Skin or Mucous Membranes,” The FASEB Journal 16 (2002): 1041–1049.

[209]

M. J. Karkkainen, A. Saaristo, L. Jussila, et al., “A Model for Gene Therapy of Human Hereditary Lymphedema,” PNAS 98 (2001): 12677–12682.

[210]

L. Jiang, W. Ren, C. Xie, et al., “Genetic Landscape of FOXC2 Mutations in Lymphedema-Distichiasis Syndrome: Different Mechanism of Pathogenicity for Mutations in Different Domains,” Experimental Eye Research 222 (2022): 109136.

[211]

G. Brice, S. Mansour, R. Bell, et al., “Analysis of the Phenotypic Abnormalities in Lymphoedema-Distichiasis Syndrome in 74 Patients With FOXC2 Mutations or Linkage to 16q24,” Journal of Medical Genetics 39 (2002): 478–483.

[212]

A. Sabine, Y. Agalarov, H. Maby-El Hajjami, et al., “Mechanotransduction, PROX1, and FOXC2 Cooperate to Control connexin37 and Calcineurin During Lymphatic-Valve Formation,” Developmental Cell 22 (2012): 430–445.

[213]

P. Ostergaard, M. A. Simpson, F. C. Connell, et al., “Mutations in GATA2 Cause Primary Lymphedema Associated With a Predisposition to Acute Myeloid Leukemia (Emberger Syndrome),” Nature Genetics 43 (2011): 929–931.

[214]

P. Brouillard, M. H. Witte, R. P. Erickson, et al., “Primary Lymphoedema,” Nature Reviews Disease Primers 7 (2021): 77.

[215]

K. Ogmen, S. E. Dobbins, R. Y. Behncke, et al., “Insights Into KIF11 Pathogenesis in Microcephaly-Lymphedema-Chorioretinopathy Syndrome From a Lymphatic Perspective,” JCI Insight 11 (2026): e177656.

[216]

V. Gelanova, D. Veselenyiova, R. Kozacikova, et al., “Genetic Variants in the Transcription Factor Network: The Impact of FOXC1, NOTCH1, RORC, FOXC2 and SOX18 in Primary Lymphedema,” Lymphology 58 (2025): 119–134.

[217]

P. Ostergaard, M. A. Simpson, G. Brice, et al., “Rapid Identification of Mutations in GJC2 in Primary Lymphoedema Using Whole Exome Sequencing Combined With Linkage Analysis With Delineation of the Phenotype,” Journal of Medical Genetics 48 (2011): 251–255.

[218]

R. E. Ferrell, C. J. Baty, M. A. Kimak, et al., “GJC2 Missense Mutations Cause Human Lymphedema,” American Journal of Human Genetics 86 (2010): 943–948.

[219]

E. Fotiou, S. Martin-Almedina, M. A. Simpson, et al., “Novel Mutations in PIEZO1 Cause an Autosomal Recessive Generalized Lymphatic Dysplasia With Non-Immune Hydrops Fetalis,” Nature Communications 6 (2015): 8085.

[220]

M. Alders, L. Al-Gazali, I. Cordeiro, et al., “Hennekam Syndrome Can be Caused by FAT4 Mutations and be Allelic to Van Maldergem Syndrome,” Human Genetics 133 (2014): 1161–1167.

[221]

M. Alders, B. M. Hogan, E. Gjini, et al., “Mutations in CCBE1 Cause Generalized Lymph Vessel Dysplasia in Humans,” Nature Genetics 41 (2009): 1272–1274.

[222]

P. Ostergaard, M. A. Simpson, A. Mendola, et al., “Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated With Congenital Lymphedema and Chorioretinopathy,” American Journal of Human Genetics 90 (2012): 356–362.

[223]

A. Irrthum, K. Devriendt, D. Chitayat, et al., “Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia,” American Journal of Human Genetics 72 (2003): 1470–1478.

[224]

S. H. Seo, S. Lee, J. K. Park, et al., “Clinical Staging and Genetic Profiling of Korean Patients With Primary Lymphedema Using Targeted Gene Sequencing,” Scientific Reports 12 (2022): 13591.

[225]

C. Bowman and S. G. Rockson, “Genetic Causes of Lymphatic Disorders: Recent Updates on the Clinical and Molecular Aspects of Lymphatic Disease,” Current Opinion in Cardiology 39 (2024): 170–177.

[226]

K. Gordon, R. Varney, V. Keeley, et al., “Update and Audit of the St George's Classification Algorithm of Primary Lymphatic Anomalies: A Clinical and Molecular Approach to Diagnosis,” Journal of Medical Genetics 57 (2020): 653–659.

[227]

M. B. Aldrich, M. E. McWain, S. F. Shaitelman, et al., “Lymphatic Pumping Failure in the Arm Precedes Dermal Backflow and Breast Cancer-Related Lymphedema,” Breast Cancer Research 28 (2026): 61.

[228]

X. Liu, M. Yuan, Q. Xiang, et al., “Single-Cell RNA Sequencing of Subcutaneous Adipose Tissues Identifies Therapeutic Targets for Cancer-Associated Lymphedema,” Cell Discovery 8 (2022): 58.

[229]

T. DiSipio, S. Rye, B. Newman, et al., “Incidence of Unilateral Arm Lymphoedema After Breast Cancer: A Systematic Review and Meta-Analysis,” The Lancet Oncology 14 (2013): 500–515.

[230]

A. Shen, Q. Lu, X. Fu, et al., “Risk Factors of Unilateral Breast Cancer-Related Lymphedema: An Updated Systematic Review and Meta-Analysis of 84 Cohort Studies,” Supportive Care in Cancer 31 (2022): 18.

[231]

M. B. Aldrich, J. C. Rasmussen, S. M. DeSnyder, et al., “Prediction of Breast Cancer-Related Lymphedema by Dermal Backflow Detected With Near-Infrared Fluorescence Lymphatic Imaging,” Breast Cancer Research and Treatment 195 (2022): 33–41.

[232]

C. Bowman and S. G. Rockson, “The Role of Inflammation in Lymphedema: A Narrative Review of Pathogenesis and Opportunities for Therapeutic Intervention,” International Journal of Molecular Sciences 25 (2024): 3907.

[233]

S. O. Lee and I. K. Kim, “Molecular Pathophysiology of Secondary Lymphedema,” Frontiers in Cell and Developmental Biology 12 (2024): 1363811.

[234]

S. Karaman, S. Lehti, C. Zhang, et al., “Multi-Omics Characterization of Lymphedema-Induced Adipose Tissue Resulting From Breast Cancer-Related Surgery,” The FASEB Journal 38 (2024): e70097.

[235]

T. Karlsson, M. Karlsson, K. Ohlin, et al., “Liposuction of Breast Cancer-Related Arm Lymphedema Reduces Fat and Muscle Hypertrophy,” Lymphatic Research and Biology 20 (2022): 53–63.

[236]

S. G. Rockson, W. Tian, X. Jiang, et al., “Pilot Studies Demonstrate the Potential Benefits of Antiinflammatory Therapy in Human Lymphedema,” JCI Insight 3 (2018): e123775.

[237]

P. Hartiala, S. Suominen, E. Suominen, et al., “Phase 1 Lymfactin(Ⓡ) Study: Short-Term Safety of Combined Adenoviral VEGF-C and Lymph Node Transfer Treatment for Upper Extremity Lymphedema,” Journal of Plastic, Reconstructive & Aesthetic Surgery 73 (2020): 1612–1621.

[238]

I. M. Leppäpuska, P. Hartiala, S. Suominen, et al., “Phase 1 Lymfactin® Study: 24-Month Efficacy and Safety Results of Combined Adenoviral VEGF-C and Lymph Node Transfer Treatment for Upper Extremity Lymphedema,” Journal of Plastic, Reconstructive & Aesthetic Surgery 75 (2022): 3938–3945.

[239]

S. Pajula, A. Saarikko, S. Suominen, et al., “Lymfactin® Gene Therapy With Vascularized Lymph Node Transfer Reduces Compression-Free Swelling and Enhances Quality of Life in Breast Cancer-Related Lymphedema: Final Phase I Trial Results,” Journal of Plastic, Reconstructive & Aesthetic Surgery 111 (2025): 312–321.

[240]

E. H. Rannikko, S. Pajula, S. H. Suominen, et al., “Phase II Study Shows the Effect of Adenoviral Vascular Endothelial Growth Factor C and Lymph Node Transfer in Lymphedema,” Plastic and Reconstructive Surgery 155 (2025): 256e–267e.

[241]

S. Brown, B. J. Mehrara, M. Coriddi, et al., “A Prospective Study on the Safety and Efficacy of Vascularized Lymph Node Transplant,” Annals of Surgery 276 (2022): 635–653.

[242]

Y. Liu, X. Long, and J. Guan, “Tissue Dielectric Constant Combined With Arm Volume Measurement as Complementary Methods in Detection and Assessment of Breast Cancer-Related Lymphedema,” Lymphatic Research and Biology 20 (2022): 26–32.

[243]

K. M. Pfarr, A. Y. Debrah, S. Specht, et al., “Filariasis and Lymphoedema,” Parasite Immunology 31 (2009): 664–672.

[244]

S. Mand, A. Y. Debrah, U. Klarmann, et al., “Doxycycline Improves Filarial Lymphedema Independent of Active Filarial Infection: A Randomized Controlled Trial,” Clinical Infectious Diseases 55 (2012): 621–630.

[245]

S. Krishnasastry, A. Ashok, A. Devidas, et al., “Efficacy and Safety of Adding 6 Weeks of Doxycycline to the Essential Package of Care to Treat Filarial Lymphedema: A Double-Blind, Randomized, Controlled Trial in Southern India,” American Journal of Tropical Medicine and Hygiene 111 (2024): 83–93.

[246]

A. Ngenya, U. Klarmann-Schulz, W. John, et al., “Efficacy of Intensified Hygiene Measures With or Without the Addition of Doxycycline in the Management of Filarial Lymphedema: A Randomized Double-Blind, Placebo-Controlled Clinical Trial in Tanzania,” American Journal of Tropical Medicine and Hygiene 111 (2024): 33–51.

[247]

Q. Liang, L. Zhang, H. Xu, et al., “Lymphatic Muscle Cells Contribute to Dysfunction of the Synovial Lymphatic System in Inflammatory Arthritis in Mice,” Arthritis Research & Therapy 23 (2021): 58.

[248]

Y. Zhang, Q. Zhao, Z. Wu, et al., “Mesenteric Lymphatic B Cells Migrate to the Gut and Aggravate TNBS-Induced Rat Colitis via Regulating Intestinal T Cells,” International Journal of Molecular Sciences 26 (2025): 3519.

[249]

R. S. Czepielewski, E. C. Erlich, E. J. Onufer, et al., “Ileitis-Associated Tertiary Lymphoid Organs Arise at Lymphatic Valves and Impede Mesenteric Lymph Flow in Response to Tumor Necrosis Factor,” Immunity 54 (2021): 2795–2811.e9.

[250]

R. V. Heatley, P. M. Bolton, L. E. Hughes, et al., “Mesenteric Lymphatic Obstruction in Crohn's Disease,” Digestion 20 (1980): 307–313.

[251]

M. Kodama, D. Kobayashi, K. Abe, et al., “Epithelioid Cell Granulomas in Crohn's Disease Are Differentially Associated With Blood Vessels and Lymphatic Vessels: A Sequential Double Immunostaining Study,” Journal of Histochemistry and Cytochemistry 68 (2020): 553–560.

[252]

R. Sura, J. F. Colombel, and H. J. Van Kruiningen, “Lymphatics, Tertiary Lymphoid Organs and the Granulomas of Crohn's Disease: An Immunohistochemical Study,” Alimentary Pharmacology & Therapeutics 33 (2011): 930–939.

[253]

F. Pedica, C. Ligorio, P. Tonelli, et al., “Lymphangiogenesis in Crohn's Disease: An Immunohistochemical Study Using Monoclonal Antibody D2-40,” Virchows Archiv 452 (2008): 57–63.

[254]

S. Geleff, S. F. Schoppmann, and G. Oberhuber, “Increase in Podoplanin-Expressing Intestinal Lymphatic Vessels in Inflammatory Bowel Disease,” Virchows Archiv 442 (2003): 231–237.

[255]

J. F. Rahier, L. Dubuquoy, J. F. Colombel, et al., “Decreased Lymphatic Vessel Density Is Associated With Postoperative Endoscopic Recurrence in Crohn's Disease,” Inflammatory Bowel Diseases 19 (2013): 2084–2090.

[256]

S. D'Alessio, C. Correale, C. Tacconi, et al., “VEGF-C-Dependent Stimulation of Lymphatic Function Ameliorates Experimental Inflammatory Bowel Disease,” Journal of Clinical Investigation 124 (2014): 3863–3878.

[257]

X. L. Wang, J. Zhao, L. Qin, et al., “Promoting Inflammatory Lymphangiogenesis by Vascular Endothelial Growth Factor-C (VEGF-C) Aggravated Intestinal Inflammation in Mice With Experimental Acute Colitis,” Brazilian Journal of Medical and Biological Research 49 (2016): e4738.

[258]

G. Jurisic, J. P. Sundberg, and M. Detmar, “Blockade of VEGF Receptor-3 Aggravates Inflammatory Bowel Disease and Lymphatic Vessel Enlargement,” Inflammatory Bowel Diseases 19 (2013): 1983–1989.

[259]

A. Henno, S. Blacher, C. A. Lambert, et al., “Histological and Transcriptional Study of Angiogenesis and Lymphangiogenesis in Uninvolved Skin, Acute Pinpoint Lesions and Established Psoriasis Plaques: An Approach of Vascular Development Chronology in Psoriasis,” Journal of Dermatological Science 57 (2010): 162–169.

[260]

A. E. Moustou, P. Alexandrou, A. J. Stratigos, et al., “Expression of Lymphatic Markers and Lymphatic Growth Factors in Psoriasis Before and After Anti-TNF Treatment,” Anais Brasileiros De Dermatologia 89 (2014): 891–897.

[261]

H. Boki, T. Kimura, T. Miyagaki, et al., “Lymphatic Dysfunction Exacerbates Cutaneous Tumorigenesis and Psoriasis-Like Skin Inflammation Through Accumulation of Inflammatory Cytokines,” Journal of Investigative Dermatology 142 (2022): 1692–1702.e3.

[262]

S. Cliff, A. J. Bedlow, A. W. Stanton, et al., “An in Vivo Study of the Microlymphatics in Psoriasis Using Fluorescence Microlymphography,” British Journal of Dermatology 140 (1999): 61–66.

[263]

R. Huggenberger, S. Ullmann, S. T. Proulx, et al., “Stimulation of Lymphangiogenesis via VEGFR-3 Inhibits Chronic Skin Inflammation,” Journal of Experimental Medicine 207 (2010): 2255–2269.

[264]

V. Y. Shi, L. Bao, and L. S. Chan, “Inflammation-Driven Dermal Lymphangiogenesis in Atopic Dermatitis Is Associated With CD11b+ Macrophage Recruitment and VEGF-C Up-Regulation in the IL-4-Transgenic Mouse Model,” Microcirculation 19 (2012): 567–579.

[265]

M. Böhm, B. Riemann, T. A. Luger, et al., “Bilateral Upper Limb Lymphoedema Associated With Psoriatic Arthritis: A Case Report and Review of the Literature,” British Journal of Dermatology 143 (2000): 1297–1301.

[266]

Q. Zhang, Y. Lu, S. T. Proulx, et al., “Increased Lymphangiogenesis in Joints of Mice With Inflammatory Arthritis,” Arthritis Research & Therapy 9 (2007): R118.

[267]

R. Guo, Q. Zhou, S. T. Proulx, et al., “Inhibition of Lymphangiogenesis and Lymphatic Drainage via Vascular Endothelial Growth Factor Receptor 3 Blockade Increases the Severity of Inflammation in a Mouse Model of Chronic Inflammatory Arthritis,” Arthritis and Rheumatism 60 (2009): 2666–2676.

[268]

Q. Liang, Y. Ju, Y. Chen, et al., “Lymphatic Endothelial Cells Efferent to Inflamed Joints Produce iNOS and Inhibit Lymphatic Vessel Contraction and Drainage in TNF-Induced Arthritis in Mice,” Arthritis Research & Therapy 18 (2016): 62.

[269]

J. P. Scallan, E. M. Bouta, H. Rahimi, et al., “Ex Vivo Demonstration of Functional Deficiencies in Popliteal Lymphatic Vessels From TNF-Transgenic Mice With Inflammatory Arthritis,” Frontiers in Physiology 12 (2021): 745096.

[270]

F. N. de Jesus and P. Y. von der Weid, “Increased Contractile Activity and Dilation of Popliteal Lymphatic Vessels in the TNF-α-Overexpressing TNF(ΔARE/+) Arthritic Mouse,” Life Sciences 335 (2023): 122247.

[271]

S. Zhou, G. Zhao, R. Chen, et al., “Lymphatic Vessels: Roles and Potential Therapeutic Intervention in Rheumatoid Arthritis and Osteoarthritis,” Theranostics 14 (2024): 265–282.

[272]

E. M. Bouta, I. Kuzin, K. de Mesy Bentley, et al., “Brief Report: Treatment of Tumor Necrosis Factor-Transgenic Mice With Anti-Tumor Necrosis Factor Restores Lymphatic Contractions, Repairs Lymphatic Vessels, and May Increase Monocyte/Macrophage Egress,” Arthritis & Rheumatology 69 (2017): 1187–1193.

[273]

A. Manzo, F. Benaglio, B. Vitolo, et al., “Power Doppler Ultrasonographic Assessment of the Joint-Draining Lymph Node Complex in Rheumatoid Arthritis: A Prospective, Proof-of-Concept Study on Treatment With Tumor Necrosis Factor Inhibitors,” Arthritis Research & Therapy 18 (2016): 242.

[274]

T. Fukuda, R. Kayama, S. Ogiwara, et al., “Comparison of the Axillary Lymph Node Between Rheumatoid Arthritis and Psoriatic Arthritis With Computed Tomography,” Acta Radiologica Open 11 (2022): 20584601221112616.

[275]

A. Rossi, F. Sozio, P. Sestini, et al., “Lymphatic and Blood Vessels in Scleroderma Skin, a Morphometric Analysis,” Human Pathology 41 (2010): 366–374.

[276]

M. Manetti, A. F. Milia, S. Guiducci, et al., “Progressive Loss of Lymphatic Vessels in Skin of Patients With Systemic Sclerosis,” Journal of Rheumatology 38 (2011): 297–301.

[277]

A. Akhmetshina, J. Beer, K. Zwerina, et al., “Decreased Lymphatic Vessel Counts in Patients With Systemic Sclerosis: Association With Fingertip Ulcers,” Arthritis and Rheumatism 62 (2010): 1513–1522.

[278]

I. Rosa, E. Romano, B. S. Fioretto, et al., “Lymphatic Endothelial-To-Myofibroblast Transition: A Potential New Mechanism Underlying Skin Fibrosis in Systemic Sclerosis,” Cells 12 (2023): 2195.

[279]

M. J. Howlader, W. G. Ambler, M. L. S. Chalasani, et al., “Lymphatic Dysfunction in Lupus Contributes to Cutaneous Photosensitivity and Lymph Node B Cell Responses,” Journal of Clinical Investigation 135 (2025): e168412.

[280]

T. Wang, W. Li, J. H. Yeom, et al., “Inhibition of VEGFR-3 by SAR131675 Decreases Renal Inflammation and Lymphangiogenesis in the Murine Lupus Nephritis Model,” Cell Death Discovery 11 (2025): 320.

[281]

P. Pekkonen, S. Alve, G. Balistreri, et al., “Lymphatic Endothelium Stimulates Melanoma Metastasis and Invasion via MMP14-Dependent Notch3 and β1-Integrin Activation,” Elife 7 (2018): e32490.

[282]

M. Van de Velde, M. Ebroin, T. Durré, et al., “Tumor Exposed-Lymphatic Endothelial Cells Promote Primary Tumor Growth via IL6,” Cancer Letters 497 (2021): 154–164.

[283]

W. F. Wei, H. L. Zhou, P. Y. Chen, et al., “Cancer-Associated Fibroblast-Derived PAI-1 Promotes Lymphatic Metastasis via the Induction of EndoMT in Lymphatic Endothelial Cells,” Journal of Experimental & Clinical Cancer Research 42 (2023): 160.

[284]

S. S. Dadras, B. Lange-Asschenfeldt, P. Velasco, et al., “Tumor Lymphangiogenesis Predicts Melanoma Metastasis to Sentinel Lymph Nodes,” Modern Pathology 18 (2005): 1232–1242.

[285]

Y. Nakamura, H. Yasuoka, M. Tsujimoto, et al., “Lymph Vessel Density Correlates With Nodal Status, VEGF-C Expression, and Prognosis in Breast Cancer,” Breast Cancer Research and Treatment 91 (2005): 125–132.

[286]

Y. Zeng, K. Opeskin, L. G. Horvath, et al., “Lymphatic Vessel Density and Lymph Node Metastasis in Prostate Cancer,” Prostate 65 (2005): 222–230.

[287]

N. Audet, N. J. Beasley, C. MacMillan, et al., “Lymphatic Vessel Density, Nodal Metastases, and Prognosis in Patients With Head and Neck Cancer,” Archives of Otolaryngology – Head and Neck Surgery 131 (2005): 1065–1070.

[288]

S. Zhang, S. Yi, D. Zhang, et al., “Intratumoral and Peritumoral Lymphatic Vessel Density Both Correlate With Lymph Node Metastasis in Breast Cancer,” Scientific Reports 7 (2017): 40364.

[289]

Y. Gao, Z. Liu, F. Gao, et al., “High Density of Peritumoral Lymphatic Vessels Is a Potential Prognostic Marker of Endometrial Carcinoma: A Clinical Immunohistochemical Method Study,” BMC Cancer 10 (2010): 131.

[290]

S. J. Mandriota, L. Jussila, M. Jeltsch, et al., “Vascular Endothelial Growth Factor-C-Mediated Lymphangiogenesis Promotes Tumour Metastasis,” The EMBO Journal 20 (2001): 672–682.

[291]

M. Skobe, T. Hawighorst, D. G. Jackson, et al., “Induction of Tumor Lymphangiogenesis by VEGF-C Promotes Breast Cancer Metastasis,” Nature Medicine 7 (2001): 192–198.

[292]

Y. He, K. Kozaki, T. Karpanen, et al., “Suppression of Tumor Lymphangiogenesis and Lymph Node Metastasis by Blocking Vascular Endothelial Growth Factor Receptor 3 Signaling,” JNCI: Journal of the National Cancer Institute 94 (2002): 819–825.

[293]

S. A. Stacker, C. Caesar, M. E. Baldwin, et al., “VEGF-D Promotes the Metastatic Spread of Tumor Cells via the Lymphatics,” Nature Medicine 7 (2001): 186–191.

[294]

V. Joukov, K. Pajusola, A. Kaipainen, et al., “A Novel Vascular Endothelial Growth Factor, VEGF-C, Is a Ligand for the Flt4 (VEGFR-3) and KDR (VEGFR-2) Receptor Tyrosine Kinases,” The EMBO Journal 15 (1996): 290–298.

[295]

N. Roberts, B. Kloos, M. Cassella, et al., “Inhibition of VEGFR-3 Activation With the Antagonistic Antibody More Potently Suppresses Lymph Node and Distant Metastases Than Inactivation of VEGFR-2,” Cancer Research 66 (2006): 2650–2657.

[296]

S. Hirakawa, L. F. Brown, S. Kodama, et al., “VEGF-C-Induced Lymphangiogenesis in Sentinel Lymph Nodes Promotes Tumor Metastasis to Distant Sites,” Blood 109 (2007): 1010–1017.

[297]

J. D. Shields, I. C. Kourtis, A. A. Tomei, et al., “Induction of Lymphoidlike Stroma and Immune Escape by Tumors That Express the Chemokine CCL21,” Science 328 (2010): 749–752.

[298]

H. Takeuchi, A. Fujimoto, M. Tanaka, et al., “CCL21 Chemokine Regulates Chemokine Receptor CCR7 Bearing Malignant Melanoma Cells,” Clinical Cancer Research 10 (2004): 2351–2358.

[299]

M. Miyamoto, Y. Kawato, R. Fujie, et al., “CCL21-Ser Expression in Melanoma Cells Recruits CCR7(+) Naïve T Cells to Tumor Tissues and Promotes Tumor Growth,” Cancer Science 114 (2023): 3509–3522.

[300]

R. Fujie, K. Kurowarabe, Y. Yamada, et al., “Endogenous CCL21-Ser Deficiency Reduces B16-F10 Melanoma Growth by Enhanced Antitumor Immunity,” Heliyon 9 (2023): e19215.

[301]

T. H. Pham, P. Baluk, Y. Xu, et al., “Lymphatic Endothelial Cell Sphingosine Kinase Activity Is Required for Lymphocyte Egress and Lymphatic Patterning,” Journal of Experimental Medicine 207 (2010): 17–27.

[302]

E. Sibler, Y. He, L. Ducoli, et al., “Immunomodulatory Responses of Subcapsular Sinus Floor Lymphatic Endothelial Cells in Tumor-Draining Lymph Nodes,” Cancers (Basel) 14 (2022): 3602.

[303]

A. W. Lund, F. V. Duraes, S. Hirosue, et al., “VEGF-C Promotes Immune Tolerance in B16 Melanomas and Cross-Presentation of Tumor Antigen by Lymph Node Lymphatics,” Cell Reports 1 (2012): 191–199.

[304]

S. Alve, S. Gramolelli, J. Jukonen, et al., “DLL4/Notch3/WNT5B Axis Mediates Bidirectional Prometastatic Crosstalk Between Melanoma and Lymphatic Endothelial Cells,” JCI Insight 9 (2024): e171821.

[305]

S. Roy, S. Kumaravel, P. Banerjee, et al., “Tumor Lymphatic Interactions Induce CXCR2-CXCL5 Axis and Alter Cellular Metabolism and Lymphangiogenic Pathways to Promote Cholangiocarcinoma,” Cells 10 (2021): 3093.

[306]

L. C. Dieterich, K. Kapaklikaya, T. Cetintas, et al., “Transcriptional Profiling of Breast Cancer-Associated Lymphatic Vessels Reveals VCAM-1 as Regulator of Lymphatic Invasion and Permeability,” International Journal of Cancer 145 (2019): 2804–2815.

[307]

M. Xia, L. Yuan, L. Chen, et al., “CREB5 Promotes Nodal Metastasis of Cervical Cancer by Regulation of APLN-Induced Lymphangiogenesis,” Cell Death Discovery 11 (2025): 488.

[308]

J. Shi, Y. J. Li, B. Yan, et al., “Interleukin-8: A Potent Promoter of Human Lymphatic Endothelial Cell Growth in Gastric Cancer,” Oncology Reports 33 (2015): 2703–2710.

[309]

J. Xu, C. Zhang, Y. He, et al., “Lymphatic Endothelial Cell-Secreted CXCL1 Stimulates Lymphangiogenesis and Metastasis of Gastric Cancer,” International Journal of Cancer 130 (2012): 787–797.

[310]

T. Naruse, T. Goi, and A. Yamaguchi, “Prokineticin-1 Induces Normal Lymphangiogenic Activity and Is Involved in Lymphangiogenesis and Lymph Node Metastasis in Colorectal Cancer,” Oncotarget 12 (2021): 1388–1397.

[311]

C. Tacconi, C. Correale, A. Gandelli, et al., “Vascular Endothelial Growth Factor C Disrupts the Endothelial Lymphatic Barrier to Promote Colorectal Cancer Invasion,” Gastroenterology 148 (2015): 1438–1451.e8.

[312]

Y. Zeng, K. Opeskin, J. Goad, et al., “Tumor-Induced Activation of Lymphatic Endothelial Cells via Vascular Endothelial Growth Factor Receptor-2 Is Critical for Prostate Cancer Lymphatic Metastasis,” Cancer Research 66 (2006): 9566–9575.

[313]

T. He, W. Tao, J. Zhang, et al., “Extracellular Vesicle-Mediated Transmission of circPDLIM5 Promotes Lymphatic Metastasis in Prostate Cancer,” Journal of Experimental & Clinical Cancer Research 44 (2025): 188.

[314]

T. Shah, F. Wildes, S. Kakkad, et al., “Lymphatic Endothelial Cells Actively Regulate Prostate Cancer Cell Invasion,” NMR in Biomedicine 29 (2016): 904–911.

[315]

L. Zhu, Y. Bai, A. Li, et al., “IFN-γ-Responsiveness of Lymphatic Endothelial Cells Inhibits Melanoma Lymphatic Dissemination via AMPK-Mediated Metabolic Control,” Biochim Biophys Acta Mol Basis Dis 1870 (2024): 167314.

[316]

T. Karakousi, V. Cristaldi, M. L. Lopes de Oliveira, et al., “IFNγ-Dependent Metabolic Reprogramming Restrains an Immature, Pro-Metastatic Lymphatic State in Melanoma,” Cancer Cell 44 (2026): 792–808.e9.

[317]

M. Sun, L. Garnier, R. Chevalier, et al., “Lymphatic-Derived Oxysterols Promote Anti-Tumor Immunity and Response to Immunotherapy in Melanoma,” Nature Communications 16 (2025): 1217.

[318]

M. M. Mattila, J. K. Ruohola, T. Karpanen, et al., “VEGF-C Induced Lymphangiogenesis Is Associated With Lymph Node Metastasis in Orthotopic MCF-7 Tumors,” International Journal of Cancer 98 (2002): 946–951.

[319]

T. Karpanen, M. Egeblad, M. J. Karkkainen, et al., “Vascular Endothelial Growth Factor C Promotes Tumor Lymphangiogenesis and Intralymphatic Tumor Growth,” Cancer Research 61 (2001): 1786–1790.

[320]

K. Jennbacken, C. Vallbo, W. Wang, et al., “Expression of Vascular Endothelial Growth Factor C (VEGF-C) and VEGF Receptor-3 in Human Prostate Cancer Is Associated With Regional Lymph Node Metastasis,” Prostate 65 (2005): 110–116.

[321]

V. Pagliarulo, D. Hawes, F. H. Brands, et al., “Detection of Occult Lymph Node Metastases in Locally Advanced Node-Negative Prostate Cancer,” Journal of Clinical Oncology 24 (2006): 2735–2742.

[322]

A. Marini, R. Zakopoulou, G. Ntritsos, et al., “The Prognostic Value of Lymphatic Vessel Density in Squamous Cell Carcinoma of the Tongue: A Systematic Review and Meta-Analysis,” European Archives of Oto-Rhino-Laryngology 283 (2025): 2681–2688.

[323]

S. Zhang, D. Zhang, M. Gong, et al., “High Lymphatic Vessel Density and Presence of Lymphovascular Invasion Both Predict Poor Prognosis in Breast Cancer,” BMC Cancer 17 (2017): 335.

[324]

M. Watanabe, H. Tanaka, M. Ohira, et al., “Intranodal Lymphangiogenesis Precedes Development of Lymph Node Metastasis and Accelerates Progression of Gastric Cancer,” Journal of Gastrointestinal Surgery 18 (2014): 481–490.

[325]

S. H. Wang, J. S. Chang, J. R. Hsiao, et al., “Tumour Cell-Derived WNT5B Modulates in Vitro Lymphangiogenesis via Induction of Partial Endothelial-Mesenchymal Transition of Lymphatic Endothelial Cells,” Oncogene 36 (2017): 1503–1515.

[326]

Z. Pu, Y. Shimizu, T. Hayashi, et al., “Cardiac Lymphatic Insufficiency Leads to Diastolic Dysfunction via Myocardial Morphologic Change,” JACC: Basic to Translational Science 8 (2023): 958–972.

[327]

E. Cao, M. J. Watt, C. J. Nowell, et al., “Mesenteric Lymphatic Dysfunction Promotes Insulin Resistance and Represents a Potential Treatment Target in Obesity,” Nature Metabolism 3 (2021): 1175–1188.

[328]

E. Brakenhielm, “Cardiac Lymphatic Dysfunction and Repair in Cardiovascular Disease,” Nature Reviews Cardiology (2026), https://doi.org/10.1038/s41569–026–01271–1.

[329]

J. Zhou, T. Wei, and Z. He, “ADSCs Enhance VEGFR3-Mediated Lymphangiogenesis via METTL3-Mediated VEGF-C M(6)A Modification to Improve Wound Healing of Diabetic Foot Ulcers,” Molecular Medicine 27 (2021): 146.

[330]

L. M. Brunner, Y. He, N. Cousin, et al., “Promotion of Lymphangiogenesis by Targeted Delivery of VEGF-C Improves Diabetic Wound Healing,” Cells 12 (2023): 472.

[331]

B. L. Pollack, J. S. Torrisi, G. E. Hespe, et al., “Inhibition of Th2 Differentiation Accelerates Chronic Wound Healing by Facilitating Lymphangiogenesis,” Biomedicines 13 (2025): 1026.

[332]

W. Enns, A. von Rossum, and J. Choy, “Mouse Model of Alloimmune-Induced Vascular Rejection and Transplant Arteriosclerosis,” Journal of Visualized Experiments: JoVE no. 99 (2015): e52800.

[333]

Y. P. Lu, W. G. Chen, I. Wang, et al., “A New Rat Model of Transplant Arteriosclerosis Accelerated by Ischemia/Reperfusion Injury,” Transplantation Proceedings 35 (2003): 184–186.

[334]

J. Waltenberger, M. L. Akyürek, M. Aurivillius, et al., “Ischemia-Induced Transplant Arteriosclerosis in the Rat. Induction of Peptide Growth Factor Expression,” Arteriosclerosis, Thrombosis, and Vascular Biology 16 (1996): 1516–1523.

[335]

R. A. Geerling, R. W. de Bruin, M. Scheringa, et al., “Suppression of Acute Rejection Prevents Graft Arteriosclerosis After Allogeneic Aorta Transplantation in the Rat,” Transplantation 58 (1994): 1258–1263.

[336]

A. Mennander, S. Tiisala, J. Halttunen, et al., “Chronic Rejection in Rat Aortic Allografts. An Experimental Model for Transplant Arteriosclerosis,” Arteriosclerosis and Thrombosis 11 (1991): 671–680.

[337]

T. Rademakers, E. P. van der Vorst, I. T. Daissormont, et al., “Adventitial Lymphatic Capillary Expansion Impacts on Plaque T Cell Accumulation in Atherosclerosis,” Scientific Reports 7 (2017): 45263.

[338]

K. P. Yeo, H. Y. Lim, C. H. Thiam, et al., “Efficient Aortic Lymphatic Drainage Is Necessary for Atherosclerosis Regression Induced by Ezetimibe,” Science Advances 6 (2020): eabc2697.

[339]

A. Ehrlich, G. Pelli, B. Foglia, et al., “Protective Role of Pannexin1 in Lymphatic Endothelial Cells in the Progression of Atherosclerosis in Female Mice,” PLoS One 19 (2024): e0315511.

[340]

L. Vachon, G. Jean, A. Milasan, et al., “Platelet Extracellular Vesicles Preserve Lymphatic Endothelial Cell Integrity and Enhance Lymphatic Vessel Function,” Communications Biology 7 (2024): 975.

[341]

A. C. Newby, “Metalloproteinases and Vulnerable Atherosclerotic Plaques,” Trends in Cardiovascular Medicine 17 (2007): 253–258.

[342]

P. R. Moreno, K. R. Purushothaman, V. Fuster, et al., “Plaque Neovascularization Is Increased in Ruptured Atherosclerotic Lesions of Human Aorta: Implications for Plaque Vulnerability,” Circulation 110 (2004): 2032–2038.

[343]

T. Nakano, Y. Nakashima, Y. Yonemitsu, et al., “Angiogenesis and Lymphangiogenesis and Expression of Lymphangiogenic Factors in the Atherosclerotic Intima of Human Coronary Arteries,” Human Pathology 36 (2005): 330–340.

[344]

B. J. Dunmore, M. J. McCarthy, A. R. Naylor, et al., “Carotid Plaque Instability and Ischemic Symptoms Are Linked to Immaturity of Microvessels Within Plaques,” Journal of Vascular Surgery 45 (2007): 155–159.

[345]

K. Roh, H. Li, R. N. Freeman, et al., “Exercise-Induced Cardiac Lymphatic Remodeling Mitigates Inflammation in the Aging Heart,” Aging Cell 24 (2025): e70043.

[346]

L. Su, Y. Cui, M. Wu, et al., “VEGFC/VEGFR3 Signaling-Dependent Lymphatic Remodeling Modulates Cardiac Response to Pressure Overload,” Journal of the American Heart Association 14 (2025): e040649.

[347]

Q. Y. Lin, Y. L. Zhang, J. Bai, et al., “VEGF-C/VEGFR-3 Axis Protects Against Pressure-Overload Induced Cardiac Dysfunction Through Regulation of Lymphangiogenesis,” Clinical and Translational Medicine 11 (2021): e374.

[348]

C. Heron, A. Dumesnil, M. Houssari, et al., “Regulation and Impact of Cardiac Lymphangiogenesis in Pressure-Overload-Induced Heart Failure,” Cardiovascular Research 119 (2023): 492–505.

[349]

T. C. S. Keller 4th, L. Lim, S. V. Shewale, et al., “Genetic Blockade of Lymphangiogenesis Does Not Impair Cardiac Function After Myocardial Infarction,” Journal of Clinical Investigation 131 (2021): e147070.

[350]

H. Zhang, H. Jiang, W. Xie, et al., “LNPs-Mediated VEGF-C mRNA Delivery Promotes Heart Repair and Attenuates Inflammation by Stimulating Lymphangiogenesis Post-Myocardial Infarction,” Biomaterials 322 (2025): 123410.

[351]

L. Chen, X. Yang, K. Wang, et al., “Humanin Inhibits Lymphatic Endothelial Cells Dysfunction to Alleviate Myocardial Infarction-Reperfusion Injury via BNIP3-Mediated Mitophagy,” Free Radical Research 58 (2024): 180–193.

[352]

S. Deng, K. Zhao, Z. Cai, et al., “Lymphatic Endothelial C-C Motif Chemokine Ligand 2 Enhances Lymphangiogenesis and Lymphatic Clearance of Macrophages Following Myocardial Infarction,” Journal of the American Heart Association 15 (2026): e039153.

[353]

H. Gong, T. Wang, X. Sun, et al., “Fibroblasts Facilitate Lymphatic Vessel Formation in Transplanted Heart,” Theranostics 14 (2024): 1886–1908.

[354]

A. Dashkevich, A. Raissadati, S. O. Syrjälä, et al., “Ischemia-Reperfusion Injury Enhances Lymphatic Endothelial VEGFR3 and Rejection in Cardiac Allografts,” American Journal of Transplantation 16 (2016): 1160–1172.

[355]

L. A. Edwards, A. K. Nowocin, N. V. Jafari, et al., “Chronic Rejection of Cardiac Allografts Is Associated With Increased Lymphatic Flow and Cellular Trafficking,” Circulation 137 (2018): 488–503.

[356]

T. R. Soong, A. P. Pathak, H. Asano, et al., “Lymphatic Injury and Regeneration in Cardiac Allografts,” Transplantation 89 (2010): 500–508.

[357]

S. C. Ginn, A. Dragan, B. A. Niclou, et al., “Cardiac Lymphatics Predict Survival After Heart Transplantation,” Journal of the American Heart Association 15 (2026): e045005.

[358]

C. Zhou, L. Ma, H. Xu, et al., “Meningeal Lymphatics Regulate Radiotherapy Efficacy Through Modulating Anti-Tumor Immunity,” Cell Research 32 (2022): 543–554.

[359]

M. A. Kovacs, M. N. Cowan, I. W. Babcock, et al., “Meningeal Lymphatic Drainage Promotes T Cell Responses Against Toxoplasma Gondii but Is Dispensable for Parasite Control in the Brain,” Elife 11 (2022): e80775.

[360]

E. Song, T. Mao, H. Dong, et al., “VEGF-C-Driven Lymphatic Drainage Enables Immunosurveillance of Brain Tumours,” Nature 577 (2020): 689–694.

[361]

L. S. B. Boisserand, L. H. Geraldo, J. Bouchart, et al., “VEGF-C Prophylaxis Favors Lymphatic Drainage and Modulates Neuroinflammation in a Stroke Model,” Journal of Experimental Medicine 221 (2024): e20221983.

[362]

M. H. Keuters, S. Antila, R. Immonen, et al., “The Impact of VEGF-C-Induced Dural Lymphatic Vessel Growth on Ischemic Stroke Pathology,” Translational Stroke Research 16 (2025): 781–799.

[363]

H. Dong, X. Dai, Y. Zhou, et al., “Enhanced Meningeal Lymphatic Drainage Ameliorates Lipopolysaccharide-Induced Brain Injury in Aged Mice,” Journal of Neuroinflammation 21 (2024): 36.

[364]

R. Shimada, Y. Tatara, and K. Kibayashi, “Gene Expression in Meningeal Lymphatic Endothelial Cells Following Traumatic Brain Injury in Mice,” PLoS One 17 (2022): e0273892.

[365]

J. Liao, M. Zhang, Z. Shi, et al., “Improving the Function of Meningeal Lymphatic Vessels to Promote Brain Edema Absorption After Traumatic Brain Injury,” Journal of Neurotrauma 40 (2023): 383–394.

[366]

A. C. Bolte, A. B. Dutta, M. E. Hurt, et al., “Meningeal Lymphatic Dysfunction Exacerbates Traumatic Brain Injury Pathogenesis,” Nature Communications 11 (2020): 4524.

[367]

M. Wang, C. Yan, X. Li, et al., “Non-Invasive Modulation of Meningeal Lymphatics Ameliorates Ageing and Alzheimer's Disease-Associated Pathology and Cognition in Mice,” Nature Communications 15 (2024): 1453.

[368]

Y. Wu, T. Zhang, X. Li, et al., “Borneol-Driven Meningeal Lymphatic Drainage Clears Amyloid-β Peptide to Attenuate Alzheimer-Like Phenotype in Mice,” Theranostics 13 (2023): 106–124.

[369]

C. Choi, J. Park, H. Kim, et al., “DSCR1 Upregulation Enhances Dural Meningeal Lymphatic Drainage to Attenuate Amyloid Pathology of Alzheimer's Disease,” Journal of Pathology 255 (2021): 296–310.

[370]

T. Reiter, A. L. Dörrler, N. Hasenauer, et al., “Molecular Imaging of Lymphatic Organs Provides Prognostic Value After Acute Myocardial Infarction,” European Journal of Nuclear Medicine and Molecular Imaging 53 (2026): 4700–4707.

[371]

Y. Ahn, H. J. Koo, J. Choe, et al., “Single-Center Experience With Dynamic Contrast-Enhanced Magnetic Resonance Lymphangiography for Diagnosing Lymphatic Disorders and Guiding Percutaneous Embolization,” Journal of Korean Medical Science 39 (2024): e260.

[372]

S. Obana, S. Itakura, M. Murahashi, et al., “Reconstruction of the Lymphatic System by Transplantation of a Centrifuge-Based Bioengineered Lymphatic Tissue,” Nature Communications 16 (2025): 10154.

[373]

S. Kraus and E. Lee, “A Human Initial Lymphatic Chip Reveals Distinct Mechanisms of Primary Lymphatic Valve Dysfunction in Acute and Chronic Inflammation,” Lab on A Chip 23 (2023): 5180–5194.

[374]

Z. Li, S. Antila, H. Nurmi, et al., “Blockade of VEGFR3 Signaling Leads to Functional Impairment of Dural Lymphatic Vessels Without Affecting Autoimmune Neuroinflammation,” Science Immunology 8 (2023): eabq0375.

[375]

Y. S. Yoon, T. Murayama, E. Gravereaux, et al., “VEGF-C Gene Therapy Augments Postnatal Lymphangiogenesis and Ameliorates Secondary Lymphedema,” Journal of Clinical Investigation 111 (2003): 717–725.

[376]

A. Saaristo, T. Veikkola, T. Tammela, et al., “Lymphangiogenic Gene Therapy With Minimal Blood Vascular Side Effects,” Journal of Experimental Medicine 196 (2002): 719–730.

[377]

P. Brouillard, L. Dupont, R. Helaers, et al., “Loss of ADAMTS3 Activity Causes Hennekam Lymphangiectasia-Lymphedema Syndrome 3,” Human Molecular Genetics 26 (2017): 4095–4104.

[378]

H. M. Bui, D. Enis, M. R. Robciuc, et al., “Proteolytic Activation Defines Distinct Lymphangiogenic Mechanisms for VEGFC and VEGFD,” Journal of Clinical Investigation 126 (2016): 2167–2180.

[379]

M. Jeltsch, S. K. Jha, D. Tvorogov, et al., “CCBE1 Enhances Lymphangiogenesis via A Disintegrin and Metalloprotease With Thrombospondin Motifs-3-Mediated Vascular Endothelial Growth Factor-C Activation,” Circulation 129 (2014): 1962–1971.

[380]

V. Joukov, T. Sorsa, V. Kumar, et al., “Proteolytic Processing Regulates Receptor Specificity and Activity of VEGF-C,” The EMBO Journal 16 (1997): 3898–3911.

[381]

Z. Ocskay, L. Bálint, C. Christ, et al., “CCBE1 Regulates the Development and Prevents the Age-Dependent Regression of Meningeal Lymphatics,” Biomedicine & Pharmacotherapy 170 (2024): 116032.

[382]

L. Dupont, L. Joannes, F. Morfoisse, et al., “ADAMTS2 and ADAMTS14 Can Substitute for ADAMTS3 in Adults for Pro-VEGFC Activation and Lymphatic Homeostasis,” JCI Insight 7 (2022): e151509.

[383]

P. Juneja, S. N. Ruhina Rahman, D. Jakhar, et al., “Recombinant VEGF-C (Cys156Ser) Improves Mesenteric Lymphatic Drainage and Gut Immune Surveillance in Experimental Cirrhosis,” JHEP Reports 5 (2023): 100816.

[384]

J. Goldman, T. X. Le, M. Skobe, et al., “Overexpression of VEGF-C Causes Transient Lymphatic Hyperplasia but Not Increased Lymphangiogenesis in Regenerating Skin,” Circulation Research 96 (2005): 1193–1199.

[385]

M. T. Visuri, K. M. Honkonen, P. Hartiala, et al., “VEGF-C and VEGF-C156S in the Pro-Lymphangiogenic Growth Factor Therapy of Lymphedema: A Large Animal Study,” Angiogenesis 18 (2015): 313–326.

[386]

Y. Liu, Y. Fang, P. Dong, et al., “Effect of Vascular Endothelial Growth Factor C (VEGF-C) Gene Transfer in Rat Model of Secondary Lymphedema,” Vascul Pharmacol 48 (2008): 150–156.

[387]

B. Liu, M. Jin, C. Ma, et al., “An Engineered Lymph Node Comprising Porous Collagen Scaffold With Hybridized Biological Signals Embedded in B Cell Membrane Coatings,” Biomaterials 304 (2024): 122420.

[388]

S. Landau, A. Newman, S. Edri, et al., “Investigating Lymphangiogenesis in Vitro and in Vivo Using Engineered Human Lymphatic Vessel Networks,” PNAS 118 (2021): e2101931118.

[389]

Y. Saito, H. Nakagami, R. Morishita, et al., “Transfection of Human Hepatocyte Growth Factor Gene Ameliorates Secondary Lymphedema via Promotion of Lymphangiogenesis,” Circulation 114 (2006): 1177–1184.

[390]

K. Kajiya, S. Hirakawa, B. Ma, et al., “Hepatocyte Growth Factor Promotes Lymphatic Vessel Formation and Function,” The EMBO Journal 24 (2005): 2885–2895.

[391]

D. Jin, K. Harada, S. Ohnishi, et al., “Adrenomedullin Induces Lymphangiogenesis and Ameliorates Secondary Lymphoedema,” Cardiovascular Research 80 (2008): 339–345.

[392]

T. Onishi, T. Nishizuka, T. Kurahashi, et al., “Topical bFGF Improves Secondary Lymphedema Through Lymphangiogenesis in a Rat Tail Model,” Plastic and Reconstructive Surgery – Global Open 2 (2014): e196.

[393]

E. Michalaki, J. M. Rudd, L. Liebman, et al., “Lentiviral Overexpression of VEGFC in Transplanted MSCs Leads to Resolution of Swelling in a Mouse Tail Lymphedema Model,” Microcirculation 30 (2023): e12792.

[394]

Z. Xue, D. Yang, Z. Jin, et al., “IGF-1 Secreted by Mesenchymal Stem Cells Affects the Function of Lymphatic Endothelial Progenitor Cells: A Potential Strategy for the Treatment of Lymphedema,” Frontiers in Genetics 16 (2025): 1584095.

[395]

R. Ogino, K. Hayashida, S. Yamakawa, et al., “Adipose-Derived Stem Cells Promote Intussusceptive Lymphangiogenesis by Restricting Dermal Fibrosis in Irradiated Tissue of Mice,” International Journal of Molecular Sciences 21 (2020): 3885.

[396]

S. Yoshida, R. Hamuy, Y. Hamada, et al., “Adipose-Derived Stem Cell Transplantation for Therapeutic Lymphangiogenesis in a Mouse Secondary Lymphedema Model,” RegenMed 10 (2015): 549–562.

[397]

N. M. Toyserkani, C. H. Jensen, S. P. Sheikh, et al., “Cell-Assisted Lipotransfer Using Autologous Adipose-Derived Stromal Cells for Alleviation of Breast Cancer-Related Lymphedema,” STEM CELLS Translational Medicine 5 (2016): 857–859.

[398]

D. C. Andersen, F. A. Bjerre, M. G. Jørgensen, et al., “Clinical Outcome Is Unlinked to Injection of Adipose-Derived Regenerative Cells in the Axilla of Breast Cancer-Related Lymphedema Patients,” Stem Cell Research & Therapy 15 (2024): 426.

[399]

M. G. Jørgensen, N. M. Toyserkani, C. H. Jensen, et al., “Adipose-Derived Regenerative Cells and Lipotransfer in Alleviating Breast Cancer-Related Lymphedema: An Open-Label Phase I Trial With 4 Years of Follow-Up,” STEM CELLS Translational Medicine 10 (2021): 844–854.

[400]

N. M. Toyserkani, C. H. Jensen, S. Tabatabaeifar, et al., “Adipose-Derived Regenerative Cells and Fat Grafting for Treating Breast Cancer-Related Lymphedema: Lymphoscintigraphic Evaluation With 1 Year of Follow-Up,” Journal of Plastic, Reconstructive & Aesthetic Surgery 72 (2019): 71–77.

[401]

N. M. Toyserkani, C. H. Jensen, D. C. Andersen, et al., “Treatment of Breast Cancer-Related Lymphedema With Adipose-Derived Regenerative Cells and Fat Grafts: A Feasibility and Safety Study,” STEM CELLS Translational Medicine 6 (2017): 1666–1672.

[402]

M. G. Jørgensen, C. H. Jensen, A. P. Hermann, et al., “No Clinical Efficacy of Adipose-Derived Regenerative Cells and Lipotransfer in Breast Cancer-Related Lymphedema: A Double-Blind Placebo-Controlled Phase II Trial,” Plastic and Reconstructive Surgery 154 (2024): 1172–1182.

[403]

N. Ahmadzadeh, J. W. Robering, A. Kengelbach-Weigand, et al., “Human Adipose-Derived Stem Cells Support Lymphangiogenesis in Vitro by Secretion of Lymphangiogenic Factors,” Experimental Cell Research 388 (2020): 111816.

[404]

A. Yan, T. Avraham, J. C. Zampell, et al., “Adipose-Derived Stem Cells Promote Lymphangiogenesis in Response to VEGF-C Stimulation or TGF-β1 Inhibition,” Future oncology 7 (2011): 1457–1473.

[405]

W. Tian, S. G. Rockson, X. Jiang, et al., “Leukotriene B(4) Antagonism Ameliorates Experimental Lymphedema,” Science Translational Medicine 9 (2017): eaal3920.

[406]

M. García-Caballero, A. Zecchin, J. Souffreau, et al., “Role and Therapeutic Potential of Dietary Ketone Bodies in Lymph Vessel Growth,” Nature Metabolism 1 (2019): 666–675.

[407]

K. P. Gomes, J. Korodimas, E. Liu, et al., “Saturated Fatty Acids Induce Lipotoxicity in Lymphatic Endothelial Cells Contributing to Secondary Lymphedema Development,” EMBO Molecular Medicine 17 (2025): 2384–2408.

[408]

I. Lodewijckx, C. Matthys, J. Verheijen, et al., “Potential Therapeutic Effect of a Ketogenic Diet for the Treatment of Lymphoedema: Results of an Exploratory Study,” Journal of Human Nutrition and Dietetics 37 (2024): 885–891.

[409]

K. Nakamura, K. Radhakrishnan, Y. M. Wong, et al., “Anti-Inflammatory Pharmacotherapy With Ketoprofen Ameliorates Experimental Lymphatic Vascular Insufficiency in Mice,” PLoS One 4 (2009): e8380.

[410]

S. Kashiwagi, K. Hosono, T. Suzuki, et al., “Role of COX-2 in Lymphangiogenesis and Restoration of Lymphatic Flow in Secondary Lymphedema,” Laboratory Investigation 91 (2011): 1314–1325.

[411]

F. Dalaei, A. Bucan, A. Wiinholt, et al., “Short Term Treatment of Secondary Lymphedema With Hyaluronidase Injections Reduces Mouse Hindlimb Lymphedema,” Journal of Plastic Surgery and Hand Surgery 58 (2023): 40–47.

[412]

H. J. Jeong, K. H. Roh, G. C. Kim, et al., “Hyaluronidase Treatment of Acute Lymphedema in a Mouse Tail Model,” Lymphology 46 (2013): 160–172.

[413]

G. K. Lee, D. P. Perrault, A. Bouz, et al., “Prolymphangiogenic Effects of 9-Cis Retinoic Acid Are Enhanced at Sites of Lymphatic Injury and Dependent on Treatment Duration in Experimental Postsurgical Lymphedema,” Lymphatic Research and Biology 20 (2022): 640–650.

[414]

I. Choi, S. Lee, H. Kyoung Chung, et al., “9-Cis Retinoic Acid Promotes Lymphangiogenesis and Enhances Lymphatic Vessel Regeneration: Therapeutic Implications of 9-Cis Retinoic Acid for Secondary Lymphedema,” Circulation 125 (2012): 872–882.

[415]

T. Kimura, T. S. Hamazaki, M. Sugaya, et al., “Cilostazol Improves Lymphatic Function by Inducing Proliferation and Stabilization of Lymphatic Endothelial Cells,” Journal of Dermatological Science 74 (2014): 150–158.

[416]

S. A. Kim, M. N. Gelvosa, H. Cheon, et al., “The Effects of Postoperative Treadmill Exercise on Rats With Secondary Lymphedema,” PLoS One 18 (2023): e0285384.

[417]

M. Kubo, T. S. Li, T. Kamota, et al., “Extracorporeal Shock Wave Therapy Ameliorates Secondary Lymphedema by Promoting Lymphangiogenesis,” Journal of Vascular Surgery 52 (2010): 429–434.

[418]

J. P. Zhou, Y. Y. Lin, M. F. Zhu, et al., “Clinical Effects of Extracorporeal Shock Wave Combined With Complex Decongestive Therapy in the Treatment of Lower Limb Lymphedema After Cervical Cancer Surgery,” Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi 41 (2025): 543–551.

[419]

E. Joos, I. Vultureanu, T. Nonneman, et al., “Low-Energy Extracorporeal Shockwave Therapy as a Therapeutic Option for Patients With a Secondary Late-Stage Fibro-Lymphedema After Breast Cancer Therapy: A Pilot Study,” Lymphatic Research and Biology 19 (2021): 175–180.

[420]

M. Matsumoto, S. Roufail, R. Inder, et al., “Signaling for Lymphangiogenesis via VEGFR-3 Is Required for the Early Events of Metastasis,” Clinical & Experimental Metastasis 30 (2013): 819–832.

[421]

S. You, S. Li, L. Zeng, et al., “Lymphatic-Localized Treg-mregDC Crosstalk Limits Antigen Trafficking and Restrains Anti-Tumor Immunity,” Cancer Cell 42 (2024): 1415–1433.e12.

[422]

M. M. Steele, A. Jaiswal, I. Delclaux, et al., “T Cell Egress via Lymphatic Vessels Is Tuned by Antigen Encounter and Limits Tumor Control,” Nature Immunology 24 (2023): 664–675.

[423]

C. Viúdez-Pareja, E. Kreft, and M. García-Caballero, “Immunomodulatory Properties of the Lymphatic Endothelium in the Tumor Microenvironment,” Frontiers in Immunology 14 (2023): 1235812.

[424]

M. Petkova, M. Kraft, S. Stritt, et al., “Immune-Interacting Lymphatic Endothelial Subtype at Capillary Terminals Drives Lymphatic Malformation,” Journal of Experimental Medicine 220 (2023): e20220741.

[425]

S. F. Schoppmann, P. Birner, J. Stöckl, et al., “Tumor-Associated Macrophages Express Lymphatic Endothelial Growth Factors and Are Related to Peritumoral Lymphangiogenesis,” American Journal of Pathology 161 (2002): 947–956.

[426]

C. Wang, J. Xu, X. Cheng, et al., “Anti-Lymphangiogenesis for Boosting Drug Accumulation in Tumors,” Signal Transduction and Targeted Therapy 9 (2024): 89.

[427]

M. Caunt, J. Mak, W. C. Liang, et al., “Blocking Neuropilin-2 Function Inhibits Tumor Cell Metastasis,” Cancer Cell 13 (2008): 331–342.

[428]

L. Chen, P. Hamrah, C. Cursiefen, et al., “Vascular Endothelial Growth Factor Receptor-3 Mediates Induction of Corneal Alloimmunity,” Nature Medicine 10 (2004): 813–815.

[429]

A. R. Hajrasouliha, T. Funaki, Z. Sadrai, et al., “Vascular Endothelial Growth Factor-C Promotes Alloimmunity by Amplifying Antigen-Presenting Cell Maturation and Lymphangiogenesis,” Investigative Ophthalmology & Visual Science 53 (2012): 1244–1250.

[430]

K. Maisel, C. L. Hrusch, J. E. G. Medellin, et al., “Pro-Lymphangiogenic VEGFR-3 Signaling Modulates Memory T Cell Responses in Allergic Airway Inflammation,” Mucosal Immunology 14 (2021): 144–151.

[431]

M. W. Saif, J. A. Knost, E. G. Chiorean, et al., “Phase 1 Study of the Anti-Vascular Endothelial Growth Factor Receptor 3 Monoclonal Antibody LY3022856/IMC-3C5 in Patients With Advanced and Refractory Solid Tumors and Advanced Colorectal Cancer,” Cancer Chemotheraphy and Pharmacology 78 (2016): 815–824.

[432]

M. R. Paillasse, M. Esquerré, F. A. Bertrand, et al., “Targeting Tumor Angiogenesis With the Selective VEGFR-3 Inhibitor EVT801 in Combination With Cancer Immunotherapy,” Cancer Research Communications 2 (2022): 1504–1519.

[433]

E. F. Tewalt, J. N. Cohen, S. J. Rouhani, et al., “Lymphatic Endothelial Cells—key Players in Regulation of Tolerance and Immunity,” Frontiers in Immunology 3 (2012): 305.

[434]

X. Wang, A. Zhang, Q. Yu, et al., “Single-Cell RNA Sequencing and Spatial Transcriptomics Reveal Pathogenesis of Meningeal Lymphatic Dysfunction After Experimental Subarachnoid Hemorrhage,” Advanced science (Weinheim, Baden-Wurttemberg, Germany) 10 (2023): e2301428.

[435]

M. Fankhauser, M. A. S. Broggi, L. Potin, et al., “Tumor Lymphangiogenesis Promotes T Cell Infiltration and Potentiates Immunotherapy in Melanoma,” Science Translational Medicine 9 (2017): eaal4712.

[436]

A. W. Lund, M. Wagner, M. Fankhauser, et al., “Lymphatic Vessels Regulate Immune Microenvironments in Human and Murine Melanoma,” Journal of Clinical Investigation 126 (2016): 3389–3402.

[437]

N. Bordry, M. A. S. Broggi, K. de Jonge, et al., “Lymphatic Vessel Density Is Associated With CD8(+) T Cell Infiltration and Immunosuppressive Factors in Human Melanoma,” Oncoimmunology 7 (2018): e1462878.

[438]

J. N. Cohen, E. F. Tewalt, S. J. Rouhani, et al., “Tolerogenic Properties of Lymphatic Endothelial Cells Are Controlled by the Lymph Node Microenvironment,” PLoS One 9 (2014): e87740.

[439]

J. Lin, Y. Chen, H. Zhu, et al., “Lymphatic Reconstruction in Kidney Allograft Aggravates Chronic Rejection by Promoting Alloantigen Presentation,” Frontiers in Immunology 12 (2021): 796260.

[440]

Y. Sakurai, N. Abe, K. Yoshikawa, et al., “Targeted Delivery of Lipid Nanoparticle to Lymphatic Endothelial Cells via Anti-Podoplanin Antibody,” Journal of Controlled Release 349 (2022): 379–387.

[441]

X. W. He, T. Liu, Y. X. Chen, et al., “Calcium Carbonate Nanoparticle Delivering Vascular Endothelial Growth Factor-C siRNA Effectively Inhibits Lymphangiogenesis and Growth of Gastric Cancer in Vivo,” Cancer Gene Therapy 15 (2008): 193–202.

[442]

X. W. He, T. Liu, Y. Xiao, et al., “Vascular Endothelial Growth Factor-C siRNA Delivered via Calcium Carbonate Nanoparticle Effectively Inhibits Lymphangiogenesis and Growth of Colorectal Cancer in Vivo,” Cancer Biotherapy & Radiopharmaceuticals 24 (2009): 249–259.

[443]

T. Li, G. D. Wang, Y. Z. Tan, et al., “Inhibition of Lymphangiogenesis of Endothelial Progenitor Cells With VEGFR-3 siRNA Delivered With PEI-Alginate Nanoparticles,” International Journal of Biological Sciences 10 (2014): 160–170.

[444]

Y. Sakurai, K. Yoshikawa, K. Arai, et al., “siRNA Delivery to Lymphatic Endothelial Cells via ApoE-Mediated Uptake by Lipid Nanoparticles,” Journal of Controlled Release 353 (2023): 125–133.

[445]

V. S. Paramanandam, C. Rogers, A. Heydon-White, et al., “Indocyanine Green Lymphography-Guided Personalized Conservative Management Recommendations in Breast Cancer-Related Upper Limb Lymphedema: A Retrospective Study,” Lymphatic Research and Biology (2026). 15578585261419293.

[446]

A. Soran, K. Senol, and K. Lupinacci, “Navigating Lymphedema: The Impact of Indocyanine Green Lymphography on Personalized Therapy Outcomes in Breast Cancer Patients,” Clinical Breast Cancer 25 (2025): 19–26.

[447]

M. Zhang, J. Xie, J. Huang, et al., “Magnetic Resonance Lymphography Findings Across Different Clinical Stages of Lower Limb Lymphedema,” Journal of Plastic, Reconstructive & Aesthetic Surgery 96 (2024): 129–135.

[448]

M. Mills, G. Brezgyte, B. Ho, et al., “Magnetic Resonance Lymphangiography: Establishing Normal,” Journal of Vascular Surgery: Venous and Lymphatic Disorders 12 (2024): 101870.

[449]

M. Trevethan, E. Doig, F. Patterson, et al., “Indocyanine Green Lymphography in Conservative Lymphedema Management: An Exploration of the Impact on Lymphedema Therapy Plans,” Seminars in Oncology Nursing 41 (2025): 151792.

[450]

M. Liu, D. Luo, Y. Yang, et al., “Clinical Value of MRI in Central Lymphatic Vessel Evaluation and Grading in Primary Lower-Extremity Lymphedema,” Vascular Medicine 31 (2026): 90–99.

[451]

I. Min, S. J. Lim, G. J. Cheon, et al., “Pneumatic Compression-Assisted Lymphoscintigraphy for Quantitative Evaluation of Breast Cancer-Related Lymphedema,” Clinical Nuclear Medicine 48 (2023): 679–684.

[452]

M. G. Jørgensen, N. M. Toyserkani, F. C. G. Hansen, et al., “Prospective Validation of Indocyanine Green Lymphangiography Staging of Breast Cancer-Related Lymphedema,” Cancers (Basel) 13 (2021): 1540.

[453]

T. Yamamoto, M. Narushima, K. Doi, et al., “Characteristic Indocyanine Green Lymphography Findings in Lower Extremity Lymphedema: The Generation of a Novel Lymphedema Severity Staging System Using Dermal Backflow Patterns,” Plastic and Reconstructive Surgery 127 (2011): 1979–1986.

[454]

G. Hou, Y. Jiang, W. Xu, et al., “(68)Ga-NOTA-Evans Blue PET/CT Findings in Lymphangioleiomyomatosis Compared With (99m)TC-ASC Lymphoscintigraphy: A Prospective Study,” Orphanet journal of rare diseases 16 (2021): 279.

[455]

F. Li, Z. Zhang, J. Cai, et al., “Primary Preclinical and Clinical Evaluation of (68)Ga-DOTA-TMVP1 as a Novel VEGFR-3 PET Imaging Radiotracer in Gynecological Cancer,” Clinical Cancer Research 26 (2020): 1318–1326.

[456]

X. Chen, F. Li, Y. Si, et al., “First Evaluation of [(68)Ga]Ga-NOTA-(TMVP1)(2) for Imaging VEGFR-3 in Ovarian Cancer Patients,” American Journal of Nuclear Medicine and Molecular Imaging 15 (2025): 65–73.

[457]

T. Morales-Tisnés, L. S. De Leon-Benedetti, K. I. Ramirez-Suarez, et al., “Dynamic Contrast-Enhanced Magnetic Resonance Lymphangiography: A Simple Algorithm for Image Interpretation,” Pediatric Radiology 55 (2025): 2336–2347.

[458]

E. Gousopoulos, S. T. Proulx, S. B. Bachmann, et al., “An Important Role of VEGF-C in Promoting Lymphedema Development,” Journal of Investigative Dermatology 137 (2017): 1995–2004.

[459]

A. Szuba, M. Skobe, M. J. Karkkainen, et al., “Therapeutic Lymphangiogenesis With Human Recombinant VEGF-C,” The FASEB Journal 16 (2002): 1985–1987.

[460]

L. Schindewolffs, G. Breves, M. Buettner, et al., “VEGF-C Improves Regeneration and Lymphatic Reconnection of Transplanted Autologous Lymph Node Fragments: An Animal Model for Secondary Lymphedema Treatment,” Immunity, Inflammation and Disease 2 (2014): 152–161.

[461]

H. Bae and H. J. Kim, “Clinical Outcomes of Extracorporeal Shock Wave Therapy in Patients With Secondary Lymphedema: A Pilot Study,” Annals of Rehabilitation Medicine 37 (2013): 229–234.

[462]

F. Serizawa, K. Ito, M. Matsubara, et al., “Extracorporeal Shock Wave Therapy Induces Therapeutic Lymphangiogenesis in a Rat Model of Secondary Lymphoedema,” European Journal of Vascular and Endovascular Surgery 42 (2011): 254–260.

[463]

D. Dionyssiou, A. Tsimponis, E. Georgiadou, et al., “Long-Term Results of Lymphedema Treatment With Combined Lymph Node Transfer and Collagen Scaffolds: An Observational Study,” JPRAS Open 43 (2025): 328–339.

[464]

D. Nguyen, T. S. Zaitseva, A. Zhou, et al., “Lymphatic Regeneration After Implantation of Aligned Nanofibrillar Collagen Scaffolds: Preliminary Preclinical and Clinical Results,” Journal of Surgical Oncology 125 (2022): 113–122.

[465]

C. Hadamitzky, T. S. Zaitseva, M. Bazalova-Carter, et al., “Aligned Nanofibrillar Collagen Scaffolds—Guiding Lymphangiogenesis for Treatment of Acquired Lymphedema,” Biomaterials 102 (2016): 259–267.

[466]

M. Kanapathy, D. Kalaskar, A. Mosahebi, et al., “Development of a Tissue-Engineered Lymphatic Graft Using Nanocomposite Polymer for the Treatment of Secondary Lymphedema,” Artificial Organs 40 (2016): E1–11.

[467]

T. Dai, Z. Jiang, S. Li, et al., “Reconstruction of Lymph Vessel by Lymphatic Endothelial Cells Combined With Polyglycolic Acid Scaffolds: A Pilot Study,” Journal of Biotechnology 150 (2010): 182–189.

[468]

S. Goyal, S. K. Chauhan, and R. Dana, “Blockade of Prolymphangiogenic Vascular Endothelial Growth Factor C in Dry Eye Disease,” Archives of Ophthalmology 130 (2012): 84–89.

[469]

K. I. Ramirez-Suarez, L. O. Tierradentro-Garcia, C. L. Smith, et al., “Dynamic Contrast-Enhanced Magnetic Resonance Lymphangiography,” Pediatric Radiology 52 (2022): 285–294.

[470]

V. Triacca, E. Güç, W. W. Kilarski, et al., “Transcellular Pathways in Lymphatic Endothelial Cells Regulate Changes in Solute Transport by Fluid Stress,” Circulation Research 120 (2017): 1440–1452.

[471]

E. Kukk, A. Lymboussaki, S. Taira, et al., “VEGF-C Receptor Binding and Pattern of Expression With VEGFR-3 Suggests a Role in Lymphatic Vascular Development,” Development 122 (1996): 3829–3837.

[472]

A. Aspelund, S. Antila, S. T. Proulx, et al., “A Dural Lymphatic Vascular System That Drains Brain Interstitial Fluid and Macromolecules,” Journal of Experimental Medicine 212 (2015): 991–999.

[473]

A. Alam, I. Blanc, G. Gueguen-Dorbes, et al., “SAR131675, a Potent and Selective VEGFR-3-TK Inhibitor With Antilymphangiogenic, Antitumoral, and Antimetastatic Activities,” Molecular Cancer Therapeutics 11 (2012): 1637–1649.

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