Mechanical Signaling: Molecular Mechanisms, Biological Functions, Diseases, and Therapeutic Targets

Yicen Long , Peng Wang , Jiacheng Lei , Baihai Su , Qiang Wei , Xiaojing Liu

MedComm ›› 2025, Vol. 6 ›› Issue (12) : e70523

PDF
MedComm ›› 2025, Vol. 6 ›› Issue (12) :e70523 DOI: 10.1002/mco2.70523
REVIEW
Mechanical Signaling: Molecular Mechanisms, Biological Functions, Diseases, and Therapeutic Targets
Author information +
History +
PDF

Abstract

Cell mechanics is a fundamental regulator of numerous cellular processes, orchestrating critical biological activities spanning from embryogenesis to senescence. Cells continuously sense and respond to mechanical cues through specialized interactions between membrane-bound adhesion proteins, such as integrins, and adhesive ligands within the extracellular matrix (ECM). This bidirectional interaction forms the basis of mechanotransduction—a complex, dynamic process that ultimately leads to alterations in nuclear mechanics and governs essential cellular functions, including migration, tissue morphogenesis, and so on. In this review, we provide an overview of these dynamic cell–ECM interactions and delve into the intricate molecular mechanisms underlying mechanotransduction. We further introduce advanced research methodologies and emerging clinical tools used to investigate cellular mechanical phenotype, mechanotransduction, and diseases progression. In addition, we analyzed the roles of mechanical biomarkers in the development and progression of cancer, fibrosis, and aging. We highlighted the necessity of drug development targeting mechanotransduction, providing examples of drugs that have already entered clinical trials and preclinical tools. By integrating current findings and outlining emerging perspectives, this review aims to provide critical insights and inspire future efforts in understanding, manipulating, and clinically exploiting mechanotransduction-targeted markers to regulate the progression of diseases such as cancer, fibrosis, and aging.

Keywords

mechanobiology / mechanotransduction / cancer / fibrosis / aging

Cite this article

Download citation ▾
Yicen Long, Peng Wang, Jiacheng Lei, Baihai Su, Qiang Wei, Xiaojing Liu. Mechanical Signaling: Molecular Mechanisms, Biological Functions, Diseases, and Therapeutic Targets. MedComm, 2025, 6(12): e70523 DOI:10.1002/mco2.70523

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

B. Innocenti, “Biomechanics: A fundamental tool With a long history (and even longer future!),” Muscles Ligaments Tendons J 7, no. 4 (2017): 491–492.

[2]

E. Ruoslahti, “The RGD story: A personal account,” Matrix Biology 22, no. 6 (2003): 459–465.

[3]

R. O. Hynes, “The emergence of integrins: A personal and historical perspective,” Matrix Biology 23, no. 6 (2004): 333–340.

[4]

M. J. Bissell, H. G. Hall, and G. Parry, “How does the extracellular matrix direct gene expression?,” Journal of Theoretical Biology 99, no. 1 (1982): 31–68.

[5]

D. E. Ingber, J. A. Madri, and J. D. Jamieson, “Role of basal lamina in neoplastic disorganization of tissue architecture,” PNAS 78, no. 6 (1981): 3901–3905.

[6]

D. E. Ingber and I. Tensegrity, “Cell structure and hierarchical systems biology,” Journal of Cell Science 116, no. Pt 7 (2003): 1157–1173.

[7]

N. Wang, J. P. Butler, and D. E. Ingber, “Mechanotransduction Across the Cell Surface and Through the Cytoskeleton,” Science 260, no. 5111 (1993): 1124–1127.

[8]

N. Wang, K. Naruse, D. Stamenović, et al., “Mechanical behavior in living cells consistent With the tensegrity model,” Proceedings of the National Academy of Sciences 98, no. 14 (2001): 7765–7770.

[9]

A. Naba, “Mechanisms of assembly and remodelling of the extracellular matrix,” Nature Reviews Molecular Cell Biology 25, no. 11 (2024): 865–885.

[10]

A. Saraswathibhatla, D. Indana, and O. Chaudhuri, “Cell–extracellular matrix mechanotransduction in 3D,” Nature Reviews Molecular Cell Biology 24, no. 7 (2023): 495–516.

[11]

M. González-Martín, G. Martínez-Ara, J. T. Ngo, X. Trepat, and P. Roca-Cusachs, “Synthetic mechanotransduction,” Nature Reviews Bioengineering (2025).

[12]

X. Di, X. Gao, L. Peng, et al., “Cellular mechanotransduction in health and diseases: From molecular mechanism to therapeutic targets,” Signal Transduction and Targeted Therapy 8, no. 1 (2023): 282.

[13]

V. D. L. Putra, K. A. Kilian, and M. L. Knothe Tate, “Biomechanical, biophysical and biochemical modulators of cytoskeletal remodelling and emergent stem cell lineage commitment,” Communications Biology 6, no. 1 (2023): 75.

[14]

S. Mascharak, J. L. Guo, M. Griffin, C. E. Berry, D. C. Wan, and M. T. Longaker, “Modelling and targeting mechanical forces in organ fibrosis,” Nature Reviews Bioengineering 2, no. 4 (2024): 305–323.

[15]

L. Chin, Y. Xia, D. E. Discher, and P. A. Janmey, “Mechanotransduction in cancer,” Current Opinion in Chemical Engineering 11 (2016): 77–84.

[16]

A. Massey, J. Stewart, C. Smith, et al., “Mechanical properties of human tumour tissues and their implications for cancer development,” Nature Reviews Physics 6, no. 4 (2024): 269–282.

[17]

C.-F. Yeh, C. Chou, and K.-C. Yang. Chapter Nine—Mechanotransduction in fibrosis: Mechanisms and treatment targets. In: Y. Fang, editor. Current Topics in Membranes (Academic Press, 2021): 279–314.

[18]

D. Duscher, Z. N. Maan, V. W. Wong, et al., “Mechanotransduction and fibrosis,” Journal of Biomechanics 47, no. 9 (2014): 1997–2005.

[19]

J. M. Phillip, I. Aifuwa, J. Walston, and D. Wirtz, “The Mechanobiology of Aging,” Annual Review of Biomedical Engineering 17 (2015): 113–141.

[20]

H. M. Han, S. Y. Kim, and D. H. Kim, “Mechanotransduction for therapeutic approaches: Cellular aging and rejuvenation,” APL Bioeng 9, no. 2 (2025): 021502.

[21]

G. Huang, F. Li, X. Zhao, et al., “Functional and Biomimetic Materials for Engineering of the Three-Dimensional Cell Microenvironment,” Chem Rev 117, no. 20 (2017): 12764–12850.

[22]

C. Frantz, K. M. Stewart, and V. M. Weaver, “The extracellular matrix at a glance,” Journal of Cell Science 123, no. Pt 24 (2010): 4195–4200.

[23]

S. J. Morrison and A. C. Spradling, “Stem cells and niches: Mechanisms that promote stem cell maintenance throughout life,” Cell 132, no. 4 (2008): 598–611.

[24]

Z. Sun, S. Wang, and R. C. Zhao, “The roles of mesenchymal stem cells in tumor inflammatory microenvironment,” Journal of Hematology & Oncology 7 (2014): 14.

[25]

X. Li, Q. Fan, X. Peng, et al., “Mesenchymal/stromal stem cells: Necessary factors in tumour progression,” Cell Death Discovery 8, no. 1 (2022): 333.

[26]

P. P. Provenzano, “Bringing order to the matrix,” Nature Materials 19, no. 2 (2020): 130–131.

[27]

A. W. Holle, J. L. Young, K. J. Van Vliet, et al., “Cell-Extracellular Matrix Mechanobiology: Forceful Tools and Emerging Needs for Basic and Translational Research,” Nano Letters 18, no. 1 (2018): 1–8.

[28]

J. C. Acosta, A. Banito, T. Wuestefeld, et al., “A complex secretory program orchestrated by the inflammasome controls paracrine senescence,” Nature Cell Biology 15, no. 8 (2013): 978–990.

[29]

D. E. Jaalouk and J. Lammerding, “Mechanotransduction gone awry,” Nature Reviews Molecular Cell Biology 10, no. 1 (2009): 63–73.

[30]

J. Kaur and D. P. Reinhardt, “Chapter 3 - Extracellular Matrix (ECM) Molecules,” In: A. Vishwakarma, P. Sharpe, S. Shi, M. Ramalingam, editors. Stem Cell Biology and Tissue Engineering in Dental Sciences (Boston: Academic Press, 2015): 25–45.

[31]

T. Zhao, Y. Huang, J. Zhu, et al., “Extracellular Matrix Signaling Cues: Biological Functions, Diseases, and Therapeutic Targets,” MedComm 6, no. 8 (2025): e70281.

[32]

T. J. McKee, G. Perlman, M. Morris, and S. V. Komarova, “Extracellular matrix composition of connective tissues: A systematic review and meta-analysis,” Scientific Reports 9, no. 1 (2019): 10542.

[33]

M. Dovedytis, Z. J. Liu, and S. Bartlett, “Hyaluronic acid and its biomedical applications: A review,” Engineered Regeneration 1 (2020): 102–113.

[34]

G. A. Monteiro, A. V. Fernandes, H. G. Sundararaghavan, and D. I. Shreiber, “Positively and negatively modulating cell adhesion to type I collagen via peptide grafting,” Tissue Engineering Part A 17, no. 13-14 (2011): 1663–1673.

[35]

A. Y. Clark, K. E. Martin, J. R. García, et al., “Integrin-specific hydrogels modulate transplanted human bone marrow-derived mesenchymal stem cell survival, engraftment, and reparative activities,” Nature Communications 11, no. 1 (2020): 114.

[36]

C. C. Wu, L. C. Wang, Y. T. Su, W. Y. Wei, and K. J. Tsai, “Synthetic α5β1 integrin ligand PHSRN is proangiogenic and neuroprotective in cerebral ischemic stroke,” Biomaterials 185 (2018): 142–154.

[37]

R. Pankov and K. M. Yamada, “Fibronectin at a glance,” Journal of Cell Science 115, no. Pt 20 (2002): 3861–3863.

[38]

L. M. Weber, K. N. Hayda, K. Haskins, and K. S. Anseth, “The effects of cell-matrix interactions on encapsulated beta-cell function Within hydrogels functionalized With matrix-derived adhesive peptides,” Biomaterials 28, no. 19 (2007): 3004–3011.

[39]

V. K. Deb and U. Jain, “Activation of transforming growth factor beta 1 Through integrin alpha V beta 6 and its molecular insights Into cancer progression, and future directions,” International Journal of Biological Macromolecules 324 (2025): 147121.

[40]

C. Margadant and A. Sonnenberg, “Integrin-TGF-beta crosstalk in fibrosis, cancer and wound healing,” Embo Reports 11, no. 2 (2010): 97–105.

[41]

S. L. Nishimura, “Integrin-mediated transforming growth factor-beta activation, a potential therapeutic target in fibrogenic disorders,” American Journal of Pathology 175, no. 4 (2009): 1362–1370.

[42]

M. M. Giacomini, M. A. Travis, M. Kudo, and D. Sheppard, “Epithelial cells utilize cortical actin/myosin to activate latent TGF-β Through integrin α(v)β(6)-dependent physical force,” Experimental Cell Research 318, no. 6 (2012): 716–722.

[43]

A. L. Berrier and K. M. Yamada, “Cell-matrix adhesion,” Journal of Cellular Physiology 213, no. 3 (2007): 565–573.

[44]

Y. A. Kadry and D. A. Calderwood, “Chapter 22: Structural and signaling functions of integrins,” Biochimica Et Biophysica Acta (BBA)—Biomembranes 1862, no. 5 (2020): 183206.

[45]

S. Schumacher, D. Dedden, R. V. Nunez, et al., “Structural insights Into integrin α(5)β(1) opening by fibronectin ligand,” Science Advances 7, no. 19 (2021): eabe9716.

[46]

A. L. Hughes, J. R. Kelley, and R. J. Klose, “Understanding the interplay Between CpG island-associated gene promoters and H3K4 methylation,” Biochim Biophys Acta Gene Regul Mech 1863, no. 8 (2020): 194567.

[47]

M. A. Arnaout, S. L. Goodman, and J. P. Xiong, “Structure and mechanics of integrin-based cell adhesion,” Current Opinion in Cell Biology 19, no. 5 (2007): 495–507.

[48]

P. Lu, K. Takai, V. M. Weaver, and Z. Werb, “Extracellular matrix degradation and remodeling in development and disease,” Cold Spring Harbor Perspectives in Biology 3, no. 12 (2011): a005058.

[49]

M. M. Martino, M. Mochizuki, D. A. Rothenfluh, S. A. Rempel, J. A. Hubbell, and T. H. Barker, “Controlling integrin specificity and stem cell differentiation in 2D and 3D environments Through regulation of fibronectin domain stability,” Biomaterials 30, no. 6 (2009): 1089–1097.

[50]

A. J. Engler, S. Sen, H. L. Sweeney, and D. E. Discher, “Matrix elasticity directs stem cell lineage specification,” Cell 126, no. 4 (2006): 677–689.

[51]

O. Chaudhuri, J. Cooper-White, P. A. Janmey, D. J. Mooney, and V. B. Shenoy, “Effects of extracellular matrix viscoelasticity on cellular behaviour,” Nature 584, no. 7822 (2020): 535–546.

[52]

Q. Sun, F. Pei, M. Zhang, B. Zhang, Y. Jin, and Z. Zhao, “Curved Nanofiber Network Induces Cellular Bridge Formation to Promote Stem Cell Mechanotransduction,” Advanced Science 10, no. 3 (2023): 2204479.

[53]

O. Chaudhuri, L. Gu, M. Darnell, et al., “Substrate stress relaxation regulates cell spreading,” Nature Communications 6 (2015): 6364.

[54]

G. Maheshwari, G. Brown, D. A. Lauffenburger, A. Wells, and L. G. Griffith, “Cell adhesion and motility depend on nanoscale RGD clustering,” Journal of Cell Science 113, no. Pt 10 (2000): 1677–1686.

[55]

K. Kyriakopoulou, Z. Piperigkou, K. Tzaferi, and N. K. Karamanos, “Trends in extracellular matrix biology,” Molecular Biology Reports 50, no. 1 (2023): 853–863.

[56]

J. Qin, O. Vinogradova, and E. F. Plow, “Integrin bidirectional signaling: A molecular view,” PLoS Biology 2, no. 6 (2004): e169.

[57]

J. Z. Kechagia, J. Ivaska, and P. Roca-Cusachs, “Integrins as biomechanical sensors of the microenvironment,” Nature Reviews Molecular Cell Biology 20, no. 8 (2019): 457–473.

[58]

C. M. Niessen, D. Leckband, and A. S. Yap, “Tissue organization by cadherin adhesion molecules: Dynamic molecular and cellular mechanisms of morphogenetic regulation,” Physiological Reviews 91, no. 2 (2011): 691–731.

[59]

J. de Wit and A. Ghosh, “Specification of synaptic connectivity by cell surface interactions,” Nature Reviews Neuroscience 17, no. 1 (2016): 4.

[60]

A. del Rio, R. Perez-Jimenez, R. Liu, P. Roca-Cusachs, J. M. Fernandez, and M. P. Sheetz, “Stretching single talin rod molecules activates vinculin binding,” Science 323, no. 5914 (2009): 638–641.

[61]

T. D. Perez and W. J. Nelson, “Cadherin adhesion: Mechanisms and molecular interactions,” Handbook of Experimental Pharmacology, no. 165 (2004): 3–21.

[62]

C. S. Srinivas, G. S. Singaraju, V. Kaur, et al., “Transient interactions drive the lateral clustering of cadherin-23 on membrane,” Communications Biology 6, no. 1 (2023): 293.

[63]

J. L. Maître and C. P. Heisenberg, “Three functions of cadherins in cell adhesion,” Current Biology 23, no. 14 (2013): R626–R633.

[64]

K. Baumann, “Cell adhesion: Cell–cell contacts With talin,” Nature Reviews Molecular Cell Biology 13 (2012): 409.

[65]

M. Chighizola, T. Dini, C. Lenardi, P. Milani, A. Podestà, and C. Schulte, “Mechanotransduction in neuronal cell development and functioning,” Biophysical Reviews 11, no. 5 (2019): 701–720.

[66]

R. O. Hynes, “The evolution of metazoan extracellular matrix,” Journal of Cell Biology 196, no. 6 (2012): 671–679.

[67]

C. C. DuFort, M. J. Paszek, and V. M. Weaver, “Balancing forces: Architectural control of mechanotransduction,” Nature Reviews Molecular Cell Biology 12, no. 5 (2011): 308–319.

[68]

M. Hofer and M. P. Lutolf, “Engineering organoids,” Nature Reviews Materials 6, no. 5 (2021): 402–420.

[69]

K. M. Yamada and M. Sixt, “Mechanisms of 3D cell migration,” Nature Reviews Molecular Cell Biology 20, no. 12 (2019): 738–752.

[70]

J. F. Bateman, R. P. Boot-Handford, and S. R. Lamandé, “Genetic diseases of connective tissues: Cellular and extracellular effects of ECM mutations,” Nature Reviews Genetics 10, no. 3 (2009): 173–183.

[71]

G. F. Weber, M. A. Bjerke, and D. W. DeSimone, “Integrins and cadherins join forces to form adhesive networks,” Journal of Cell Science 124, no. Pt 8 (2011): 1183–1193.

[72]

B. Klapholz and N. H. Brown, “Talin—the master of integrin adhesions,” Journal of Cell Science 130, no. 15 (2017): 2435–2446.

[73]

M. S. Bauer, F. Baumann, C. Daday, et al., “Structural and mechanistic insights Into mechanoactivation of focal adhesion kinase,” PNAS 116, no. 14 (2019): 6766–6774.

[74]

P. Kanchanawong and D. A. Calderwood, “Organization, dynamics and mechanoregulation of integrin-mediated cell–ECM adhesions,” Nature Reviews Molecular Cell Biology 24, no. 2 (2023): 142–161.

[75]

N. Wang, J. D. Tytell, and D. E. Ingber, “Mechanotransduction at a distance: Mechanically coupling the extracellular matrix With the nucleus,” Nature Reviews Molecular Cell Biology 10, no. 1 (2009): 75–82.

[76]

P. Oberdoerffer and D. A. Sinclair, “The role of nuclear architecture in genomic instability and ageing,” Nature Reviews Molecular Cell Biology 8, no. 9 (2007): 692–702.

[77]

K. Baumann, “FAK or talin: Who goes first?,” Nature Reviews Molecular Cell Biology 13, no. 3 (2012): 139.

[78]

L. Su, X. Li, X. Wu, et al., “Simultaneous deactivation of FAK and Src improves the pathology of hypertrophic scar,” Scientific Reports 6, no. 1 (2016): 26023.

[79]

V. Bolós, J. M. Gasent, S. López-Tarruella, and E. Grande, “The dual kinase complex FAK-Src as a promising therapeutic target in cancer,” Onco Targets Ther 3 (2010): 83–97.

[80]

J. Li, X. Zhang, Z. Hou, et al., “P130cas-FAK interaction is essential for YAP-mediated radioresistance of non-small cell lung cancer,” Cell Death & Disease 13, no. 9 (2022): 783.

[81]

D. M. Donato, L. M. Ryzhova, L. M. Meenderink, I. Kaverina, and S. K. Hanks, “Dynamics and mechanism of p130Cas localization to focal adhesions,” Journal of Biological Chemistry 285, no. 27 (2010): 20769–20779.

[82]

M. C. Brown, L. A. Cary, J. S. Jamieson, J. A. Cooper, and C. E. Turner, “Src and FAK kinases cooperate to phosphorylate paxillin kinase linker, stimulate its focal adhesion localization, and regulate cell spreading and protrusiveness,” Molecular Biology of the Cell 16, no. 9 (2005): 4316–4328.

[83]

K. L. Rossman, C. J. Der, and J. Sondek, “GEF means go: Turning on RHO GTPases With guanine nucleotide-exchange factors,” Nature Reviews Molecular Cell Biology 6, no. 2 (2005): 167–180.

[84]

K. F. Tolias, L. E. Rameh, H. Ishihara, et al., “Type I phosphatidylinositol-4-phosphate 5-kinases synthesize the novel lipids phosphatidylinositol 3,5-bisphosphate and phosphatidylinositol 5-phosphate,” Journal of Biological Chemistry 273, no. 29 (1998): 18040–18046.

[85]

C. D. Nobes and A. Hall, “Rho, rac, and cdc42 GTPases regulate the assembly of multimolecular focal complexes associated With actin stress fibers, lamellipodia, and filopodia,” Cell 81, no. 1 (1995): 53–62.

[86]

R. D. Mullins, J. A. Heuser, and T. D. Pollard, “The interaction of Arp2/3 complex With actin: Nucleation, high affinity pointed end capping, and formation of branching networks of filaments,” PNAS 95, no. 11 (1998): 6181–6186.

[87]

E. D. Goley and M. D. Welch, “The ARP2/3 complex: An actin nucleator comes of age,” Nature Reviews Molecular Cell Biology 7, no. 10 (2006): 713–726.

[88]

K. Mizuno, “Signaling mechanisms and functional roles of cofilin phosphorylation and dephosphorylation,” Cellular Signalling 25, no. 2 (2013): 457–469.

[89]

C. Vidal, B. Geny, J. Melle, M. Jandrot-Perrus, and M. Fontenay-Roupie, “Cdc42/Rac1-dependent activation of the p21-activated kinase (PAK) regulates human platelet lamellipodia spreading: Implication of the cortical-actin binding protein cortactin,” Blood 100, no. 13 (2002): 4462–4469.

[90]

A. S. Kim, L. T. Kakalis, N. Abdul-Manan, G. A. Liu, and M. K. Rosen, “Autoinhibition and activation mechanisms of the Wiskott-Aldrich syndrome protein,” Nature 404, no. 6774 (2000): 151–158.

[91]

G. Salloum, L. Jaafar, and M. El-Sibai, “Rho A and Rac1: Antagonists Moving Forward,” Tissue and Cell 65 (2020): 101364.

[92]

K. Riento and A. J. Ridley, “Rocks: Multifunctional kinases in cell behaviour,” Nature Reviews Molecular Cell Biology 4, no. 6 (2003): 446–456.

[93]

S. Narumiya, T. Ishizaki, and N. Watanabe, “Rho effectors and reorganization of actin cytoskeleton,” Febs Letters 410, no. 1 (1997): 68–72.

[94]

N. Watanabe, T. Kato, A. Fujita, T. Ishizaki, and S. Narumiya, “Cooperation Between mDia1 and ROCK in Rho-induced actin reorganization,” Nature Cell Biology 1, no. 3 (1999): 136–143.

[95]

J. Swift, I. L. Ivanovska, A. Buxboim, et al., “Nuclear lamin-A scales With tissue stiffness and enhances matrix-directed differentiation,” Science 341, no. 6149 (2013): 1240104.

[96]

A. J. Maniotis, C. S. Chen, and D. E. Ingber, “Demonstration of mechanical connections Between integrins, cytoskeletal filaments, and nucleoplasm that stabilize nuclear structure,” Proceedings of the National Academy of Sciences 94, no. 3 (1997): 849–854.

[97]

R. Pradhan, D. Ranade, and K. Sengupta, “Emerin modulates spatial organization of chromosome territories in cells on softer matrices,” Nucleic Acids Research 46, no. 11 (2018): 5561–5586.

[98]

S. Dupont, L. Morsut, M. Aragona, et al., “Role of YAP/TAZ in mechanotransduction,” Nature 474, no. 7350 (2011): 179–183.

[99]

J. Settleman, “A nuclear MAL-function links Rho to SRF,” Molecular Cell 11, no. 5 (2003): 1121–1123.

[100]

E. N. Olson and A. Nordheim, “Linking actin dynamics and gene transcription to drive cellular motile functions,” Nature Reviews Molecular Cell Biology 11, no. 5 (2010): 353–365.

[101]

P. Niethammer, “Components and Mechanisms of Nuclear Mechanotransduction,” Annual Review of Cell and Developmental Biology 37 (2021): 233–256.

[102]

K. Burridge, E. Monaghan-Benson, and D. M. Graham, “Mechanotransduction: From the cell surface to the nucleus via RhoA,” Philosophical Transactions of the Royal Society of London Series B: Biological Sciences 374, no. 1779 (2019): 20180229.

[103]

H. Q. Le, S. Ghatak, C. Y. Yeung, et al., “Mechanical regulation of transcription controls Polycomb-mediated gene silencing During lineage commitment,” Nature Cell Biology 18, no. 8 (2016): 864–875.

[104]

J. A. Simon and R. E. Kingston, “Mechanisms of polycomb gene silencing: Knowns and unknowns,” Nature Reviews Molecular Cell Biology 10, no. 10 (2009): 697–708.

[105]

W. Yuan, T. Wu, H. Fu, et al., “Dense chromatin activates Polycomb repressive complex 2 to regulate H3 lysine 27 methylation,” Science 337, no. 6097 (2012): 971–975.

[106]

M. P. Phelps, J. N. Bailey, T. Vleeshouwer-Neumann, and E. Y. Chen, “CRISPR screen identifies the NCOR/HDAC3 complex as a major suppressor of differentiation in rhabdomyosarcoma,” PNAS 113, no. 52 (2016): 15090–15095.

[107]

C. Guilluy and K. Burridge, “Nuclear mechanotransduction: Forcing the nucleus to respond,” Nucleus 6, no. 1 (2015): 19–22.

[108]

K. H. Hansen, A. P. Bracken, D. Pasini, et al., “A model for transmission of the H3K27me3 epigenetic mark,” Nature Cell Biology 10, no. 11 (2008): 1291–1300.

[109]

V. Pirrotta, “Molecular biology. How to read the chromatin Past,” Science 337, no. 6097 (2012): 919–920.

[110]

W. Li, P. Chen, J. Yu, et al., “FACT Remodels the Tetranucleosomal Unit of Chromatin Fibers for Gene Transcription,” Molecular Cell 64, no. 1 (2016): 120–133.

[111]

D. E. Olins and A. L. Olins, “Chromatin history: Our view From the bridge,” Nature Reviews Molecular Cell Biology 4, no. 10 (2003): 809–814.

[112]

M. Calao, A. Burny, V. Quivy, A. Dekoninck, and C. Van Lint, “A pervasive role of histone acetyltransferases and deacetylases in an NF-kappaB-signaling code,” Trends in Biochemical Sciences 33, no. 7 (2008): 339–349.

[113]

B. Sen, G. Uzer, R. M. Samsonraj, et al., “Intranuclear Actin Structure Modulates Mesenchymal Stem Cell Differentiation,” Stem Cells 35, no. 6 (2017): 1624–1635.

[114]

B. Schuettengruber, H. M. Bourbon, L. Di Croce, and G. Cavalli, “Genome Regulation by Polycomb and Trithorax: 70 Years and Counting,” Cell 171, no. 1 (2017): 34–57.

[115]

M. M. Nava, Y. A. Miroshnikova, L. C. Biggs, et al., “Heterochromatin-Driven Nuclear Softening Protects the Genome Against Mechanical Stress-Induced Damage,” Cell 181, no. 4 (2020): 800–817.e22.

[116]

M. J. Emmett and M. A. Lazar, “Integrative regulation of physiology by histone deacetylase 3,” Nature Reviews Molecular Cell Biology 20, no. 2 (2019): 102–115.

[117]

R. S. Stowers, A. Shcherbina, J. Israeli, et al., “Matrix stiffness induces a tumorigenic phenotype in mammary epithelium Through changes in chromatin accessibility,” Nat Biomed Eng 3, no. 12 (2019): 1009–1019.

[118]

B. C. Low, C. Q. Pan, G. V. Shivashankar, A. Bershadsky, M. Sudol, and M. Sheetz, “YAP/TAZ as mechanosensors and mechanotransducers in regulating organ size and tumor growth,” Febs Letters 588, no. 16 (2014): 2663–2670.

[119]

I. M. Moya and G. Halder, “Hippo-YAP/TAZ signalling in organ regeneration and regenerative medicine,” Nature Reviews Molecular Cell Biology 20, no. 4 (2019): 211–226.

[120]

S. Arsenian, B. Weinhold, M. Oelgeschläger, U. Rüther, and A. Nordheim, “Serum response factor is essential for mesoderm formation During mouse embryogenesis,” Embo Journal 17, no. 21 (1998): 6289–6299.

[121]

C. Le Dour, M. Chatzifrangkeskou, C. Macquart, et al., “Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations,” Nature Communications 13, no. 1 (2022): 7886.

[122]

A. Sotiropoulos, D. Gineitis, J. Copeland, and R. Treisman, “Signal-regulated activation of serum response factor is mediated by changes in actin dynamics,” Cell 98, no. 2 (1999): 159–169.

[123]

D. Gineitis and R. Treisman, “Differential usage of signal transduction pathways defines two types of serum response factor target gene,” Journal of Biological Chemistry 276, no. 27 (2001): 24531–24539.

[124]

T. Lin, L. Zeng, Y. Liu, et al., “Rho-ROCK-LIMK-cofilin pathway regulates shear stress activation of sterol regulatory element binding proteins,” Circulation Research 92, no. 12 (2003): 1296–1304.

[125]

O. Geneste, J. W. Copeland, and R. Treisman, “LIM kinase and Diaphanous cooperate to regulate serum response factor and actin dynamics,” Journal of Cell Biology 157, no. 5 (2002): 831–838.

[126]

F. Miralles, G. Posern, A. I. Zaromytidou, and R. Treisman, “Actin dynamics control SRF activity by regulation of its coactivator MAL,” Cell 113, no. 3 (2003): 329–342.

[127]

D. H. Cho, S. Aguayo, and A. X. Cartagena-Rivera, “Atomic force microscopy-mediated mechanobiological profiling of complex human tissues,” Biomaterials 303 (2023): 122389.

[128]

M. Krieg, G. Fläschner, D. Alsteens, et al., “Atomic force microscopy-based mechanobiology,” Nature Reviews Physics 1, no. 1 (2019): 41–57.

[129]

S. E. Cross, Y. S. Jin, J. Rao, and J. K. Gimzewski, “Nanomechanical analysis of cells From cancer patients,” Nature Nanotechnology 2, no. 12 (2007): 780–783.

[130]

C. Stashko, M.-K. Hayward, J. J. Northey, et al., “A convolutional neural network STIFMap reveals associations Between stromal stiffness and EMT in breast cancer,” Nature Communications 14, no. 1 (2023): 3561.

[131]

S. Iyer, R. M. Gaikwad, V. Subba-Rao, C. D. Woodworth, and I. Sokolov, “Atomic force microscopy detects differences in the surface brush of normal and cancerous cells,” Nature Nanotechnology 4, no. 6 (2009): 389–393.

[132]

J. R. Staunton, B. L. Doss, S. Lindsay, and R. Ros, “Correlating confocal microscopy and atomic force indentation reveals metastatic cancer cells stiffen During invasion Into collagen I matrices,” Scientific Reports 6 (2016): 19686.

[133]

T. Kwon, J. Park, G. Lee, et al., “Carbon Nanotube-Patterned Surface-Based Recognition of Carcinoembryonic Antigens in Tumor Cells for Cancer Diagnosis,” Journal of Physical Chemistry Letters 4, no. 7 (2013): 1126–1130.

[134]

M. G. Jones, O. G. Andriotis, J. J. W. Roberts, et al., “Nanoscale dysregulation of collagen structure-function disrupts mechano-homeostasis and mediates pulmonary fibrosis,” Elife 7 (2018): e36354.

[135]

B. Peña, M. Adbel-Hafiz, M. Cavasin, L. Mestroni, and O. Sbaizero, “Atomic Force Microscopy (AFM) Applications in Arrhythmogenic Cardiomyopathy,” International Journal of Molecular Sciences 23, no. 7 (2022): 3700.

[136]

E. Khattignavong, M. Neshatian, M. Vaez, et al., “Development of a facile method to compute collagen network pathological anisotropy using AFM imaging,” Scientific Reports 13, no. 1 (2023): 20173.

[137]

T. K. Berdyyeva, C. D. Woodworth, and I. Sokolov, “Human epithelial cells increase their rigidity With ageing in vitro: Direct measurements,” Physics in Medicine & Biology 50, no. 1 (2005): 81.

[138]

S. C. Lieber, N. Aubry, J. Pain, G. Diaz, S.-J. Kim, and S. F. Vatner, “Aging increases stiffness of cardiac myocytes measured by atomic force microscopy nanoindentation,” American Journal of Physiology-Heart and Circulatory Physiology 287, no. 2 (2004): H645–H651.

[139]

C. L. Essmann, D. Martinez-Martinez, R. Pryor, et al., “Mechanical properties measured by atomic force microscopy define health biomarkers in ageing C. elegans,” Nature Communications 11, no. 1 (2020): 1043.

[140]

A. Ashkin, J. M. Dziedzic, J. E. Bjorkholm, and S. Chu, “Observation of a single-beam gradient force optical trap for dielectric particles,” Optics Letters 11, no. 5 (1986): 288.

[141]

A. Ashkin, J. M. Dziedzic, and T. Yamane, “Optical trapping and manipulation of single cells using infrared laser beams,” Nature 330, no. 6150 (1987): 769–771.

[142]

C. J. Bustamante, Y. R. Chemla, S. Liu, and M. D. Wang, “Optical tweezers in single-molecule biophysics,” Nature Reviews Methods Primers 1 (2021): 25.

[143]

E. Spyratou, “Advanced Biophotonics Techniques: The Role of Optical Tweezers for Cells and Molecules Manipulation Associated With Cancer,” Frontiers in Physics 10 (2022): 2022.

[144]

Q. Zhao, H. W. Wang, P. P. Yu, et al., “Trapping and Manipulation of Single Cells in Crowded Environments,” Frontiers in Bioengineering and Biotechnology 8 (2020): 422.

[145]

M. Pradhan, S. Pathak, D. Mathur, and U. Ladiwala, “Optically trapping tumor cells to assess differentiation and prognosis of cancers,” Biomed Opt Express 7, no. 3 (2016): 943–948.

[146]

C. Y. Li, D. Cao, C. B. Qi, et al., “Combining Holographic Optical Tweezers With Upconversion Luminescence Encoding: Imaging-Based Stable Suspension Array for Sensitive Responding of Dual Cancer Biomarkers,” Analytical Chemistry 90, no. 4 (2018): 2639–2647.

[147]

G. U. O. Hong-Lian, L. I. U. Chun-Xiang, D. Jian-Fa, et al., “Mechanical Properties of Breast Cancer Cell Membrane Studied With Optical Tweezers,” Chinese Physics Letters 21, no. 12 (2004): 2543–2546.

[148]

M. D. Scott and J. Frydman, “Aberrant protein folding as the molecular basis of cancer,” Methods in Molecular Biology 232 (2003): 67–76.

[149]

C. J. Dalton, S. Dhakal, and C. A. Lemmon, “Measuring the biomechanical properties of cell-derived fibronectin fibrils,” Biomechanics and Modeling in Mechanobiology 24, no. 2 (2025): 455–469.

[150]

C. Schulze, F. Wetzel, T. Kueper, et al., “Stiffening of human skin fibroblasts With age,” Biophysical Journal 99, no. 8 (2010): 2434–2442.

[151]

F. H. C. Crick and A. F. W. Hughes, “The physical properties of cytoplasm: A study by means of the magnetic particle method Part I,” Experimental Experimental Cell Research 1, no. 1 (1950): 37–80.

[152]

R. Sarkar and V. V. Rybenkov, “A Guide to Magnetic Tweezers and Their Applications,” Frontiers in Physics 4 (2016): 2016.

[153]

D. Dulin, “An Introduction to Magnetic Tweezers,” Methods in Molecular Biology 2694 (2024): 375–401.

[154]

C. Janko, S. Dürr, L. E. Munoz, et al., “Magnetic drug targeting reduces the chemotherapeutic burden on circulating leukocytes,” International Journal of Molecular Sciences 14, no. 4 (2013): 7341–7355.

[155]

C. Janko, T. Ratschker, K. Nguyen, et al., “Functionalized Superparamagnetic Iron Oxide Nanoparticles (SPIONs) as Platform for the Targeted Multimodal Tumor Therapy,” Frontiers in oncology 9 (2019): 59.

[156]

Z. Su, D. Liu, L. Chen, et al., “CD44-Targeted Magnetic Nanoparticles Kill Head And Neck Squamous Cell Carcinoma Stem Cells In An Alternating Magnetic Field,” International Journal of Nanomedicine 14 (2019): 7549–7560.

[157]

S. Palanisamy and Y.-M. Wang, “Superparamagnetic iron oxide nanoparticulate system: Synthesis, targeting, drug delivery and therapy in cancer,” Dalton Transactions 48, no. 26 (2019): 9490–9515.

[158]

J. Dulińska-Litewka, A. Łazarczyk, P. Hałubiec, O. Szafrański, K. Karnas, and A. Karewicz, “Superparamagnetic Iron Oxide Nanoparticles—Current and Prospective Medical Applications,” Materials 12, no. 4 (2019): 617.

[159]

D. Dasgupta, D. Pally, D. K. Saini, R. Bhat, and A. Ghosh, “Nanomotors Sense Local Physicochemical Heterogeneities in Tumor Microenvironments*,” Angewandte Chemie (International ed in English) 59, no. 52 (2020): 23690–23696.

[160]

W. Zhu, B. C. Kim, M. Wang, et al., “TGFβ1 reinforces arterial aging in the vascular smooth muscle cell Through a long-range regulation of the cytoskeletal stiffness,” Scientific Reports 8, no. 1 (2018): 2668.

[161]

A. K. Harris, P. Wild, and D. Stopak, “Silicone rubber substrata: A new wrinkle in the study of cell locomotion,” Science 208, no. 4440 (1980): 177–179.

[162]

A. Zancla, P. Mozetic, M. Orsini, G. Forte, and A. Rainer, “A primer to traction force microscopy,” Journal of Biological Chemistry 298, no. 5 (2022): 101867.

[163]

Z. Li, J. Song, G. Mantini, et al., “Quantifying the traction force of a single cell by aligned silicon nanowire array,” Nano Letters 9, no. 10 (2009): 3575–3580.

[164]

M. D. Kelly, M. R. Pawlak, K. H. Zhan, G. A. Shamsan, W. R. Gordon, and D. J. Odde, “Mutual antagonism Between CD44 and integrins in glioblastoma cell traction and migration,” APL Bioeng 8, no. 3 (2024): 036102.

[165]

G. Cai, A. Nguyen, Y. Bashirzadeh, S. S. Lin, D. Bi, and A. P. Liu, “Compressive stress drives adhesion-dependent unjamming transitions in breast cancer cell migration,” Frontiers in Cell and Developmental Biology 10 (2022): 933042.

[166]

D. Böhringer, A. Bauer, I. Moravec, et al., “Fiber alignment in 3D collagen networks as a biophysical marker for cell contractility,” Matrix Biology 124 (2023): 39–48.

[167]

M. Azatov, S. M. Goicoechea, C. A. Otey, and A. Upadhyaya, “The actin crosslinking protein palladin modulates force generation and mechanosensitivity of tumor associated fibroblasts,” Scientific Reports 6 (2016): 28805.

[168]

A. Santos, B. E. Kirkpatrick, M. Kim, K. S. Anseth, and Y. Park, “2D co-culture model reveals a biophysical interplay Between activated fibroblasts and cancer cells,” Acta Biomaterialia 190 (2024): 264–272.

[169]

M. S. Hall, F. Alisafaei, E. Ban, et al., “Fibrous nonlinear elasticity enables positive mechanical feedback Between cells and ECMs,” PNAS 113, no. 49 (2016): 14043–14048.

[170]

P. Blázquez-Carmona, R. Ruiz-Mateos, J. Barrasa-Fano, et al., “Quantitative atlas of collagen hydrogels reveals mesenchymal cancer cell traction adaptation to the matrix nanoarchitecture,” Acta Biomaterialia 185 (2024): 281–295.

[171]

C. W. Molter, E. F. Muszynski, Y. Tao, T. Trivedi, A. Clouvel, and A. J. Ehrlicher, “Prostate cancer cells of increasing metastatic potential exhibit diverse contractile forces, cell stiffness, and motility in a microenvironment stiffness-dependent manner,” Frontiers in Cell and Developmental Biology 10 (2022): 932510.

[172]

A. Gaiko-Shcherbak, J. Eschenbruch, N. M. Kronenberg, et al., “Cell Force-Driven Basement Membrane Disruption Fuels EGF- and Stiffness-Induced Invasive Cell Dissemination From Benign Breast Gland Acini,” International Journal of Molecular Sciences 22, no. 8 (2021).

[173]

C. Mark, T. J. Grundy, P. L. Strissel, et al., “Correction: Collective forces of tumor spheroids in three-dimensional biopolymer networks,” Elife 9 (2020).

[174]

B. C. H. Cheung, X. Chen, H. J. Davis, et al., “Identification of CD44 as a key engager to hyaluronic acid-rich extracellular matrices for cell traction force generation and tumor invasion in 3D,” Matrix Biology 135 (2025): 1–11.

[175]

T. M. Cheung, J. B. Yan, J. J. Fu, J. Huang, F. Yuan, and G. A. Truskey, “Endothelial Cell Senescence Increases Traction Forces due to Age-Associated Changes in the Glycocalyx and SIRT1,” Cellular and Molecular Bioengineering 8, no. 1 (2015): 63–75.

[176]

M. J. Schafer, T. A. White, K. Iijima, et al., “Cellular senescence mediates fibrotic pulmonary disease,” Nature Communications 8 (2017): 14532.

[177]

P. Parikh, R. D. Britt, L. J. Manlove, et al., “Hyperoxia-induced Cellular Senescence in Fetal Airway Smooth Muscle Cells,” American Journal of Respiratory Cell and Molecular Biology 61, no. 1 (2019): 51–60.

[178]

R. P. Rand and A. C. Burton, “Mechanical Properties of the Red Cell Membrane. I. Membrane stiffness and intracellular pressure,” Biophysical Journal 4, no. 2 (1964): 115–135.

[179]

B. González-Bermúdez, G. V. Guinea, and G. R. Plaza, “Advances in Micropipette Aspiration: Applications in Cell Biomechanics, Models, and Extended Studies,” Biophysical Journal 116, no. 4 (2019): 587–594.

[180]

G. Song, Q. Luo, J. Qin, B. Wang, and S. Cai, “Expression of integrin beta1 and its roles on adhesion Between different cell cycle hepatocellular carcinoma cells (SMMC-7721) and human umbilical vein endothelial cells,” Colloids and Surfaces B, Biointerfaces 34, no. 4 (2004): 247–252.

[181]

G. Zhang, M. Long, Z. Z. Wu, and W. Q. Yu, “Mechanical properties of hepatocellular carcinoma cells,” World Journal of Gastroenterology 8, no. 2 (2002): 243–246.

[182]

Y. Xie, M. Wang, M. Cheng, Z. Gao, and G. Wang, “The viscoelastic behaviors of several kinds of cancer cells and normal cells,” Journal of the Mechanical Behavior of Biomedical Materials 91 (2019): 54–58.

[183]

H. Pu, N. Liu, J. Yu, et al., “Micropipette Aspiration of Single Cells for Both Mechanical and Electrical Characterization,” IEEE Transactions on Biomedical Engineering 66, no. 11 (2019): 3185–3191.

[184]

L. M. Lee and A. P. Liu, “A microfluidic pipette array for mechanophenotyping of cancer cells and mechanical gating of mechanosensitive channels,” Lab on a Chip 15, no. 1 (2015): 264–273.

[185]

Q. Guo, S. Park, and H. Ma, “Microfluidic micropipette aspiration for measuring the deformability of single cells,” Lab on a Chip 12, no. 15 (2012): 2687–2695.

[186]

P. M. Davidson, G. R. Fedorchak, S. Mondésert-Deveraux, et al., “High-throughput microfluidic micropipette aspiration device to probe time-scale dependent nuclear mechanics in intact cells,” Lab on A Chip 19, no. 21 (2019): 3652–3663.

[187]

N. Steklov, A. Srivastava, K. L. Sung, P. C. Chen, M. K. Lotz, and D. D. D'Lima, “Aging-related differences in chondrocyte viscoelastic properties,” Molecular and Cellular Biomechanics 6, no. 2 (2009): 113–119.

[188]

T. Böhler, A. Leo, A. Stadler, and O. Linderkamp, “Mechanical Fragility of Erythrocyte Membrane in Neonates and Adults,” Pediatric Research 32, no. 1 (1992): 92–96.

[189]

B. González-Bermúdez, H. Kobayashi, A. Abarca-Ortega, M. Córcoles-Lucas, M. González-Sánchez, and M. De la Fuente, “Aging is accompanied by T-cell stiffening and reduced interstitial migration Through dysfunctional nuclear organization,” Immunology 167, no. 4 (2022): 622–639.

[190]

Y. Song, X. Zhao, Q. Tian, and H. Liang, “Fundamental Concepts and Physics in Microfluidics,” Microfluidics: Fundamental, Devices and Applications (2018): 19–111.

[191]

F. Malloggi. Microfluidics: From Basic Principles to Applications. In: P. Lang, Y. Liu, editors. Soft Matter at Aqueous Interfaces (Cham: Springer International Publishing, 2016): 515–546.

[192]

A. Ajikumar and K. F. Lei, “Microfluidic Technologies in Advancing Cancer Research,” Micromachines (Basel) 15, no. 12 (2024).

[193]

M. Jouybar, J. J. F. Sleeboom, E. Vaezzadeh, C. M. Sahlgren, and J. M. J. den Toonder, “An in vitro model of cancer invasion With heterogeneous ECM created With droplet microfluidics,” Frontiers in Bioengineering and Biotechnology 11 (2023): 1267021.

[194]

P. Dimitriou, J. Li, G. Tornillo, T. McCloy, and D. Barrow, “Droplet Microfluidics for Tumor Drug-Related Studies and Programmable Artificial Cells,” Glob Chall 5, no. 7 (2021): 2000123.

[195]

A. H. Wong, H. Li, Y. Jia, et al., “Author Correction: Drug screening of cancer cell lines and human primary tumors using droplet microfluidics,” Scientific Reports 9, no. 1 (2019): 18660.

[196]

D. Molino, S. Quignard, C. Gruget, et al., “On-Chip Quantitative Measurement of Mechanical Stresses During Cell Migration With Emulsion Droplets,” Scientific Reports 6, no. 1 (2016): 29113.

[197]

A. Vaghef-Koodehi and B. H. Lapizco-Encinas, “Microscale electrokinetic-based analysis of intact cells and viruses,” Electrophoresis 43, no. 1-2 (2022): 263–287.

[198]

X. Yang, X. Niu, Z. Liu, et al., “Accurate Extraction of the Self-Rotational Speed for Cells in an Electrokinetics Force Field by an Image Matching Algorithm,” Micromachines (Basel) 8, no. 9 (2017).

[199]

S. Parlato, A. De Ninno, R. Molfetta, et al., “3D Microfluidic model for evaluating immunotherapy efficacy by tracking dendritic cell behaviour Toward tumor cells,” Scientific Reports 7, no. 1 (2017): 1093.

[200]

M. Danova, M. Torchio, and G. Mazzini, “Isolation of rare circulating tumor cells in cancer patients: Technical aspects and clinical implications,” Expert Review of Molecular Diagnostics 11, no. 5 (2011): 473–485.

[201]

S. L. Stott, R. J. Lee, S. Nagrath, et al., “Isolation and characterization of circulating tumor cells From patients With localized and metastatic prostate cancer,” Science Translational Medicine 2, no. 25 (2010): 25ra3.

[202]

A. E. Saliba, L. Saias, E. Psychari, et al., “Microfluidic sorting and multimodal typing of cancer cells in self-assembled magnetic arrays,” PNAS 107, no. 33 (2010): 14524–14529.

[203]

U. Dharmasiri, S. Balamurugan, A. A. Adams, P. I. Okagbare, A. Obubuafo, and S. A. Soper, “Highly efficient capture and enumeration of low abundance prostate cancer cells using prostate-specific membrane antigen aptamers immobilized to a polymeric microfluidic device,” Electrophoresis 30, no. 18 (2009): 3289–3300.

[204]

M. Nora Dickson, P. Tsinberg, Z. Tang, F. Z. Bischoff, T. Wilson, and E. F. Leonard, “Efficient capture of circulating tumor cells With a novel immunocytochemical microfluidic device,” Biomicrofluidics 5, no. 3 (2011): 34119–3411915.

[205]

S. L. Stott, C. H. Hsu, D. I. Tsukrov, et al., “Isolation of circulating tumor cells using a microvortex-generating herringbone-chip,” PNAS 107, no. 43 (2010): 18392–18397.

[206]

L. Zwi-Dantsis, V. Jayarajan, G. M. Church, R. D. Kamm, J. P. de Magalhães, and E. Moeendarbary, “Aging on Chip: Harnessing the Potential of Microfluidic Technologies in Aging and Rejuvenation Research,” Advanced Healthcare Materials 14, no. 20 (2025): e2500217.

[207]

T. Forster, “Energiewanderung und Fluoreszenz,” Die Naturwissenschaften 33, no. 6 (1946): 166–175.

[208]

L. Liu, F. He, Y. Yu, and Y. Wang, “Application of FRET Biosensors in Mechanobiology and Mechanopharmacological Screening,” Frontiers in Bioengineering and Biotechnology 8 (2020): 595497.

[209]

K. Wang, R. C. Andresen Eguiluz, F. Wu, B. R. Seo, C. Fischbach, and D. Gourdon, “Stiffening and unfolding of early deposited-fibronectin increase proangiogenic factor secretion by breast cancer-associated stromal cells,” Biomaterials 54 (2015): 63–71.

[210]

X. Ji, S. Xie, Y. Jiao, et al., “MT1-MMP activatable fluorogenic probes With enhanced specificity via high-affinity peptide conjugation for tumor imaging,” Biomaterials Science 8, no. 8 (2020): 2308–2317.

[211]

A. Colom, E. Derivery, S. Soleimanpour, et al., “A fluorescent membrane tension probe,” Nature Chemistry 10, no. 11 (2018): 1118–1125.

[212]

W. Li, X. Yu, F. Xie, et al., “A Membrane-Bound Biosensor Visualizes Shear Stress-Induced Inhomogeneous Alteration of Cell Membrane Tension,” Iscience 7 (2018): 180–190.

[213]

F. Chowdhury, I. T. Li, T. T. Ngo, et al., “Defining Single Molecular Forces Required for Notch Activation Using Nano Yoyo,” Nano Letters 16, no. 6 (2016): 3892–3897.

[214]

D. R. Stabley, C. Jurchenko, S. S. Marshall, and K. S. Salaita, “Visualizing mechanical tension Across membrane receptors With a fluorescent sensor,” Nature Methods 9, no. 1 (2011): 64–67.

[215]

X. Wang and T. Ha, “Defining single molecular forces required to activate integrin and notch signaling,” Science 340, no. 6135 (2013): 991–994.

[216]

Y. Zhang, Y. Qiu, A. T. Blanchard, et al., “Platelet integrins exhibit anisotropic mechanosensing and harness piconewton forces to mediate platelet aggregation,” PNAS 115, no. 2 (2018): 325–330.

[217]

R. Ma, A. V. Kellner, V. P. Ma, et al., “DNA probes that store mechanical information reveal transient piconewton forces applied by T cells,” PNAS 116, no. 34 (2019): 16949–16954.

[218]

Y. Duan, F. Szlam, Y. Hu, W. Chen, R. Li, and Y. Ke, “Detection of cellular traction forces via the force-triggered Cas12a-mediated catalytic cleavage of a fluorogenic reporter strand,” Nature Biomedical Engineering 7, no. 11 (2023): 1404–1418.

[219]

Y. Hu, H. Li, C. Zhang, J. Feng, W. Wang, and W. Chen, “DNA-based ForceChrono probes for deciphering single-molecule force dynamics in living cells,” Cell 187, no. 13 (2024): 3445–3459.e15.

[220]

F. Xu, S. Zhang, L. Ma, et al., “Quantum-enhanced diamond molecular tension microscopy for quantifying cellular forces,” Science Advances 10, no. 4 (2024): eadi5300.

[221]

X.-W. Cui, K.-N. Li, A.-J. Yi, et al., “Ultrasound elastography,” Endoscopic Ultrasound 11, no. 4 (2022): 252–274.

[222]

J. R. Grajo and R. G. Barr, “Strain elastography for prediction of breast cancer tumor grades,” Journal of Ultrasound in Medicine 33, no. 1 (2014): 129–134.

[223]

G. Sadigh, R. C. Carlos, C. H. Neal, and B. A. Dwamena, “Accuracy of quantitative ultrasound elastography for differentiation of malignant and benign breast abnormalities: A meta-analysis,” Breast Cancer Research and Treatment 134, no. 3 (2012): 923–931.

[224]

S. Raza, A. Odulate, E. M. Ong, S. Chikarmane, and C. W. Harston, “Using real-time tissue elastography for breast lesion evaluation: Our initial experience,” Journal of Ultrasound in Medicine 29, no. 4 (2010): 551–563.

[225]

L. Pallwein, M. Mitterberger, P. Struve, et al., “Real-time elastography for detecting prostate cancer: Preliminary experience,” Bju International 100, no. 1 (2007): 42–46.

[226]

L. Pallwein, M. Mitterberger, P. Struve, et al., “Comparison of sonoelastography guided biopsy With systematic biopsy: Impact on prostate cancer detection,” European Radiology 17, no. 9 (2007): 2278–2285.

[227]

S. Ahmad, R. Cao, T. Varghese, L. Bidaut, and G. Nabi, “Transrectal quantitative shear wave elastography in the detection and characterisation of prostate cancer,” Surgical Endoscopy 27, no. 9 (2013): 3280–3287.

[228]

R. Kagoya, H. Monobe, and H. Tojima, “Utility of elastography for differential diagnosis of benign and malignant thyroid nodules,” Otolaryngology - Head and Neck Surgery 143, no. 2 (2010): 230–234.

[229]

N. Ciledag, K. Arda, B. K. Aribas, E. Aktas, and S. K. Köse, “The utility of ultrasound elastography and MicroPure imaging in the differentiation of benign and malignant thyroid nodules,” Ajr American Journal of Roentgenology 198, no. 3 (2012): W244–W249.

[230]

V. Cantisani, S. Ulisse, E. Guaitoli, et al., “Q-elastography in the presurgical diagnosis of thyroid nodules With indeterminate cytology,” PLoS ONE 7, no. 11 (2012): e50725.

[231]

W. A. Berg, D. O. Cosgrove, C. J. Doré, et al., “Shear-wave elastography improves the specificity of breast US: The BE1 multinational study of 939 masses,” Radiology 262, no. 2 (2012): 435–449.

[232]

M. Łasecki, C. Olchowy, D. Sokołowska-Dąbek, A. Biel, R. Chaber, and U. Zaleska-Dorobisz, “Modified sonoelastographic scale score for lymph node assessment in lymphoma—a preliminary report,” Journal of Ultrasound 15, no. 60 (2015): 45–55.

[233]

M. H. Larsen, C. Fristrup, T. P. Hansen, C. P. Hovendal, and M. B. Mortensen, “Endoscopic ultrasound, endoscopic sonoelastography, and strain ratio evaluation of lymph nodes With histology as gold standard,” Endoscopy 44, no. 8 (2012): 759–766.

[234]

K. Nakaoka, S. Hashimoto, R. Miyahara, et al., “Current status of the diagnosis of chronic pancreatitis by ultrasonographic elastography,” Korean Journal of Internal Medicine 37, no. 1 (2022): 27–36.

[235]

R. M. S. Sigrist, J. Liau, A. E. Kaffas, M. C. Chammas, and J. K. Willmann, “Ultrasound Elastography: Review of Techniques and Clinical Applications,” Theranostics 7, no. 5 (2017): 1303–1329.

[236]

Y. Liu, R. Shi, G. Li, and M. Sun, “Photoacoustic elastography based on laser-excited shear wave,” Journal of Innovative Optical Health Sciences 17, no. 03 (2024): 2350031.

[237]

A. Evans, P. Rauchhaus, P. Whelehan, et al., “Does shear wave ultrasound independently predict axillary lymph node metastasis in women With invasive breast cancer?,” Breast Cancer Research and Treatment 143, no. 1 (2014): 153–157.

[238]

J. H. Youk, H. M. Gweon, and E. J. Son, “Shear-wave elastography in breast ultrasonography: The state of the art,” Ultrasonography 36, no. 4 (2017): 300–309.

[239]

J. M. Correas, A. M. Tissier, A. Khairoune, et al., “Prostate cancer: Diagnostic performance of real-time shear-wave elastography,” Radiology 275, no. 1 (2015): 280–289.

[240]

S. Shoji, A. Hashimoto, T. Nakamura, et al., “Novel application of three-dimensional shear wave elastography in the detection of clinically significant prostate cancer,” Biomedical Reports 8, no. 4 (2018): 373–377.

[241]

C. K. Zhao, S. G. Chen, A. Alizad, et al., “Three-Dimensional Shear Wave Elastography for Differentiating Benign From Malignant Thyroid Nodules,” Journal of Ultrasound in Medicine 37, no. 7 (2018): 1777–1788.

[242]

M. Jiang, C. Li, S. Tang, et al., “Nomogram Based on Shear-Wave Elastography Radiomics Can Improve Preoperative Cervical Lymph Node Staging for Papillary Thyroid Carcinoma,” Thyroid: Official Journal of the American Thyroid Association 30, no. 6 (2020): 885–897.

[243]

I. Kim, E. K. Kim, J. H. Yoon, et al., “Diagnostic role of conventional ultrasonography and shearwave elastography in asymptomatic patients With diffuse thyroid disease: Initial experience With 57 patients,” Yonsei Medical Journal 55, no. 1 (2014): 247–253.

[244]

C. H. Suh, Y. J. Choi, J. H. Baek, and J. H. Lee, “The diagnostic performance of shear wave elastography for malignant cervical lymph nodes: A systematic review and meta-analysis,” European Radiology 27, no. 1 (2017): 222–230.

[245]

J. Li, M. Chen, C. L. Cao, et al., “Diagnostic Performance of Acoustic Radiation Force Impulse Elastography for the Differentiation of Benign and Malignant Superficial Lymph Nodes: A Meta-analysis,” Journal of Ultrasound in Medicine 39, no. 2 (2020): 213–222.

[246]

Z. Wang, H. Yang, C. Suo, J. Wei, R. Tan, and M. Gu, “Application of Ultrasound Elastography for Chronic Allograft Dysfunction in Kidney Transplantation,” Journal of Ultrasound in Medicine 36, no. 9 (2017): 1759–1769.

[247]

X. Shi, J. Liu, X. Pu, C. Huang, X. Ma, and Y. Jin, “Clinical study on the evaluation of liver fibrosis by ultrasound elastography combined With platelet count model,” Clinical Hemorheology and Microcirculation 84, no. 2 (2023): 205–214.

[248]

A. Manduca, P. J. Bayly, R. L. Ehman, et al., “MR elastography: Principles, guidelines, and terminology,” Magnetic Resonance in Medicine 85, no. 5 (2021): 2377–2390.

[249]

Y. K. Mariappan, K. J. Glaser, and R. L. Ehman, “Magnetic resonance elastography: A review,” Clinical Anatomy 23, no. 5 (2010): 497–511.

[250]

S. Hirsch, J. Braun, and I. Sack, Magnetic resonance elastography: Physical background and medical applications. 1st ed. (Weinheim, Germany: Wiley-VCH, 2017).

[251]

P. Sango-Solanas, K. Tse Ve Koon, E. Van Reeth, H. Ratiney, F. Millioz, and C. Caussy, “Short echo time dual-frequency MR Elastography With Optimal Control RF pulses,” Scientific Reports 12, no. 1 (2022): 1406.

[252]

L. W. Hofstetter, H. Odéen, B. D. Bolster, D. A. Christensen, A. Payne, and D. L. Parker, “Magnetic resonance shear wave elastography using transient acoustic radiation force excitations and sinusoidal displacement encoding,” Physics in Medicine and Biology 66, no. 5 (2021).

[253]

S. Hoodeshenas, M. Yin, and S. K. Venkatesh, “Magnetic Resonance Elastography of Liver: Current Update,” Topics in Magnetic Resonance Imaging 27, no. 5 (2018): 319–333.

[254]

S. M. Thompson, J. Wang, V. S. Chandan, et al., “MR elastography of hepatocellular carcinoma: Correlation of tumor stiffness With histopathology features-Preliminary findings,” Magnetic Resonance Imaging 37 (2017): 41–45.

[255]

S. K. Venkatesh, M. Yin, J. F. Glockner, et al., “MR elastography of liver tumors: Preliminary results,” Ajr American Journal of Roentgenology 190, no. 6 (2008): 1534–1540.

[256]

S. Jang, J. M. Lee, D. H. Lee, et al., “Value of MR elastography for the preoperative estimation of liver regeneration capacity in patients With hepatocellular carcinoma,” Journal of Magnetic Resonance Imaging 45, no. 6 (2017): 1627–1636.

[257]

D. H. Lee, J. M. Lee, N. J. Yi, et al., “Hepatic stiffness measurement by using MR elastography: Prognostic values After hepatic resection for hepatocellular carcinoma,” European Radiology 27, no. 4 (2017): 1713–1721.

[258]

H. J. Cho, B. Kim, H. J. Kim, et al., “Liver stiffness measured by MR elastography is a predictor of early HCC recurrence After treatment,” European Radiology 30, no. 8 (2020): 4182–4192.

[259]

M. C. Murphy, J. Huston 3rd, K. J. Glaser, et al., “Preoperative assessment of meningioma stiffness using magnetic resonance elastography,” Journal of Neurosurgery 118, no. 3 (2013): 643–648.

[260]

A. Bunevicius, K. Schregel, R. Sinkus, A. Golby, and S. Patz, “REVIEW: MR elastography of brain tumors,” NeuroImage: Clinical 25 (2020): 102109.

[261]

Z. Yin, J. D. Hughes, J. D. Trzasko, et al., “Slip interface imaging based on MR-elastography preoperatively predicts meningioma-brain adhesion,” Journal of Magnetic Resonance Imaging 46, no. 4 (2017): 1007–1016.

[262]

Y. Shi, F. Gao, Y. Li, et al., “Differentiation of benign and malignant solid pancreatic masses using magnetic resonance elastography With spin-echo echo planar imaging and three-dimensional inversion reconstruction: A prospective study,” European Radiology 28, no. 3 (2018): 936–945.

[263]

Y. Liu, M. Wang, R. Ji, L. Cang, F. Gao, and Y. Shi, “Differentiation of pancreatic ductal adenocarcinoma From inflammatory mass: Added value of magnetic resonance elastography,” Clinical Radiology 73, no. 10 (2018): 865–872.

[264]

I. Sack, B. Beierbach, J. Wuerfel, et al., “The impact of aging and gender on brain viscoelasticity,” Neuroimage 46, no. 3 (2009): 652–657.

[265]

K. T. Osman, D. B. Maselli, I. S. Idilman, et al., “Liver Stiffness Measured by Either Magnetic Resonance or Transient Elastography Is Associated With Liver Fibrosis and Is an Independent Predictor of Outcomes Among Patients With Primary Biliary Cholangitis,” Journal of Clinical Gastroenterology 55, no. 5 (2021): 449–457.

[266]

S. K. Venkatesh, M. L. Wells, F. H. Miller, et al., “Magnetic resonance elastography: Beyond liver fibrosis-a case-based pictorial review,” Abdominal Radiology (New York) 43, no. 7 (2018): 1590–1611.

[267]

F. Zvietcovich and K. V. Larin, “Wave-based optical coherence elastography: The 10-year perspective,” Progress in Biomedical Engineering (Bristol, England) 4, no. 1 (2022).

[268]

B. E. Bouma, J. F. de Boer, D. Huang, et al., “Optical coherence tomography,” Nature Reviews Methods Primers 2, no. 1 (2022): 79.

[269]

D. Huang, E. A. Swanson, C. P. Lin, et al., “Optical coherence tomography,” Science 254, no. 5035 (1991): 1178–1181.

[270]

B. F. Kennedy, R. A. McLaughlin, K. M. Kennedy, et al., “Investigation of Optical Coherence Microelastography as a Method to Visualize Cancers in Human Breast Tissue,” Cancer Research 75, no. 16 (2015): 3236–3245.

[271]

E. V. Gubarkova, A. A. Sovetsky, L. A. Matveev, et al., “Nonlinear Elasticity Assessment With Optical Coherence Elastography for High-Selectivity Differentiation of Breast Cancer Tissues,” Materials (Basel) 15, no. 9 (2022).

[272]

D. A. Vorontsov, E. V. Gubarkova, M. A. Sirotkina, et al., “Multimodal Optical Coherence Tomography for Intraoperative Evaluation of Tumor Margins and Surgical Margins in Breast-Conserving Surgery,” Sovrem Tekhnologii Med 14, no. 2 (2022): 26–38.

[273]

A. A. Plekhanov, G. O. Grechkanev, E. A. Avetisyan, et al., “Quantitative Assessment of Polarization and Elastic Properties of Endometrial Tissue for Precancer/Cancer Diagnostics Using Multimodal Optical Coherence Tomography,” Diagnostics (Basel) 14, no. 19 (2024).

[274]

P. C. Huang, E. J. Chaney, E. Aksamitiene, et al., “Biomechanical sensing of in vivo magnetic nanoparticle hyperthermia-treated melanoma using magnetomotive optical coherence elastography,” Theranostics 11, no. 12 (2021): 5620–5633.

[275]

A. Mowla, R. Belford, J. Köhn-Gaone, et al., “Biomechanical assessment of chronic liver injury using quantitative micro-elastography,” Biomed Opt Express 13, no. 9 (2022): 5050–5066.

[276]

R. K. Chhetri, J. Carpenter, R. Superfine, S. H. Randell, and A. L. Oldenburg, “Magnetomotive optical coherence elastography for relating lung structure and function in Cystic Fibrosis,” Proceedings of Spie the International Society for Optical Engineering 7554 (2010): 755420.

[277]

H. S. Chawla, Y. Chen, M. Wu, et al., “Assessment of skin fibrosis in a murine model of systemic sclerosis With multifunctional optical coherence tomography,” Journal of Biomedial Optics 30, no. 3 (2025): 036007.

[278]

Y. Qu, T. Ma, Y. He, et al., “Miniature probe for mapping mechanical properties of vascular lesions using acoustic radiation force optical coherence elastography,” Scientific Reports 7, no. 1 (2017): 4731.

[279]

B. Erdogan, M. Ao, L. M. White, et al., “Cancer-associated fibroblasts promote directional cancer cell migration by aligning fibronectin,” Journal of Cell Biology 216, no. 11 (2017): 3799–3816.

[280]

K. Tang, S. Li, P. Li, et al., “Shear stress stimulates integrin β1 trafficking and increases directional migration of cancer cells via promoting deacetylation of microtubules,” Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 1867, no. 5 (2020): 118676.

[281]

J. R. W. Conway, O. Joshi, J. Kaivola, et al., “Dynamic regulation of integrin β1 phosphorylation supports invasion of breast cancer cells,” Nature Cell Biology 27, no. 6 (2025): 1021–1034.

[282]

I. Eke, Y. Deuse, S. Hehlgans, et al., “β1Integrin/FAK/cortactin signaling is essential for human head and neck cancer resistance to radiotherapy,” Journal of Clinical Investigation 122, no. 4 (2012): 1529–1540.

[283]

P. P. Provenzano, D. R. Inman, K. W. Eliceiri, and P. J. Keely, “Matrix density-induced mechanoregulation of breast cell phenotype, signaling and gene expression Through a FAK-ERK linkage,” Oncogene 28, no. 49 (2009): 4326–4343.

[284]

W. Li, Z. Liu, C. Zhao, and L. Zhai, “Binding of MMP-9-degraded fibronectin to β6 integrin promotes invasion via the FAK-Src-related Erk1/2 and PI3K/Akt/Smad-1/5/8 pathways in breast cancer,” Oncology Reports 34, no. 3 (2015): 1345–1352.

[285]

B. Cheng, W. Wan, G. Huang, Y. Li, G. M. Genin, and M. R. K. Mofrad, “Nanoscale integrin cluster dynamics controls cellular mechanosensing via FAKY397 phosphorylation,” Science Advances 6, no. 10 (2020): eaax1909.

[286]

S. T. Lim, X. L. Chen, Y. Lim, et al., “Nuclear FAK promotes cell proliferation and survival Through FERM-enhanced p53 degradation,” Molecular Cell 29, no. 1 (2008): 9–22.

[287]

A. Begum, T. Ewachiw, C. Jung, et al., “The extracellular matrix and focal adhesion kinase signaling regulate cancer stem cell function in pancreatic ductal adenocarcinoma,” PLoS ONE 12, no. 7 (2017): e0180181.

[288]

Z. Gong, K. M. Wisdom, E. McEvoy, et al., “Recursive feedback Between matrix dissipation and chemo-mechanical signaling drives oscillatory growth of cancer cell invadopodia,” Cell Reports 35, no. 4 (2021): 109047.

[289]

X. Wang, Y. Zhang, T. Feng, et al., “Fluid Shear Stress Promotes Autophagy in Hepatocellular Carcinoma Cells,” International Journal of Biological Sciences 14, no. 10 (2018): 1277–1290.

[290]

K. Lawler, E. Foran, G. O'Sullivan, A. Long, and D. Kenny, “Mobility and invasiveness of metastatic esophageal cancer are potentiated by shear stress in a ROCK- and Ras-dependent manner,” American Journal of Physiology. Cell Physiology 291, no. 4 (2006): C668–C677.

[291]

N. Xiong, S. Li, K. Tang, et al., “Involvement of caveolin-1 in low shear stress-induced breast cancer cell motility and adhesion: Roles of FAK/Src and ROCK/p-MLC pathways,” Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 1864, no. 1 (2017): 12–22.

[292]

J. G. Goetz, S. Minguet, I. Navarro-Lérida, et al., “Biomechanical remodeling of the microenvironment by stromal caveolin-1 favors tumor invasion and metastasis,” Cell 146, no. 1 (2011): 148–163.

[293]

S. Y. Wong, T. A. Ulrich, L. P. Deleyrolle, et al., “Constitutive activation of myosin-dependent contractility sensitizes glioma tumor-initiating cells to mechanical inputs and reduces tissue invasion,” Cancer Research 75, no. 6 (2015): 1113–1122.

[294]

L. Froidevaux-Klipfel, B. Targa, I. Cantaloube, H. Ahmed-Zaïd, C. Poüs, and A. Baillet, “Septin cooperation With tubulin polyglutamylation contributes to cancer cell adaptation to taxanes,” Oncotarget 6, no. 34 (2015): 36063–36080.

[295]

C. Herraiz, F. Calvo, P. Pandya, et al., “Reactivation of p53 by a Cytoskeletal Sensor to Control the Balance Between DNA Damage and Tumor Dissemination,” JNCI: Journal of the National Cancer Institute 108, no. 1 (2016).

[296]

M. Overholtzer, A. A. Mailleux, G. Mouneimne, et al., “A nonapoptotic cell death process, entosis, that occurs by cell-in-cell invasion,” Cell 131, no. 5 (2007): 966–979.

[297]

F. Tamzalit, M. S. Wang, W. Jin, M. Tello-Lafoz, V. Boyko, and J. M. Heddleston, “Interfacial actin protrusions mechanically enhance killing by cytotoxic T cells,” Science Immunology 4, no. 33 (2019).

[298]

Y. Liu, T. Zhang, H. Zhang, et al., “Cell Softness Prevents Cytolytic T-cell Killing of Tumor-Repopulating Cells,” Cancer Research 81, no. 2 (2021): 476–488.

[299]

E. Urciuoli, S. Petrini, V. D'Oria, M. Leopizzi, C. D. Rocca, and B. Peruzzi, “Nuclear Lamins and Emerin Are Differentially Expressed in Osteosarcoma Cells and Scale With Tumor Aggressiveness,” Cancers (Basel) 12, no. 2 (2020).

[300]

A. G. Liddane, C. A. McNamara, M. C. Campbell, I. Mercier, and J. M. Holaska, “Defects in Emerin-Nucleoskeleton Binding Disrupt Nuclear Structure and Promote Breast Cancer Cell Motility and Metastasis,” Molecular Cancer Research 19, no. 7 (2021): 1196–1207.

[301]

M. Reis-Sobreiro, J. F. Chen, T. Novitskaya, et al., “Emerin Deregulation Links Nuclear Shape Instability to Metastatic Potential,” Cancer Research 78, no. 21 (2018): 6086–6097.

[302]

J. Okletey, D. Angelis, T. M. Jones, C. Montagna, and E. T. Spiliotis, “An oncogenic isoform of septin 9 promotes the formation of juxtanuclear invadopodia by reducing nuclear deformability,” Cell Reports 42, no. 8 (2023): 112893.

[303]

M. E. Fernández-Sánchez, S. Barbier, J. Whitehead, et al., “Mechanical induction of the tumorigenic β-catenin pathway by tumour growth pressure,” Nature 523, no. 7558 (2015): 92–95.

[304]

T. Panciera, L. Azzolin, M. Cordenonsi, and S. Piccolo, “Mechanobiology of YAP and TAZ in physiology and disease,” Nature Reviews Molecular Cell Biology 18, no. 12 (2017): 758–770.

[305]

X. Cai, K. C. Wang, and Z. Meng, “Mechanoregulation of YAP and TAZ in Cellular Homeostasis and Disease Progression,” Frontiers in Cell and Developmental Biology 9 (2021): 673599.

[306]

Y. Sun, Y. Shao, X. Xue, and J. Fu. Emerging Roles of YAP/TAZ in Mechanobiology. In: S. Chien, A. J. Engler, and P. Y. Wang, editors. Molecular and Cellular Mechanobiology (New York, NY: Springer New York, 2016): 83–96.

[307]

R. J. Pelham and Y. Wang, “Cell locomotion and focal adhesions are regulated by substrate flexibility,” PNAS 94, no. 25 (1997): 13661–13665.

[308]

R. Huang and E. K. Rofstad, “Integrins as therapeutic targets in the organ-specific metastasis of human malignant melanoma,” Journal of Experimental & Clinical Cancer Research 37, no. 1 (2018): 92.

[309]

J. M. Murphy, Y. A. R. Rodriguez, K. Jeong, E. E. Ahn, and S. S. Lim, “Targeting focal adhesion kinase in cancer cells and the tumor microenvironment,” Experimental & Molecular Medicine 52, no. 6 (2020): 877–886.

[310]

A. Serrels, T. Lund, B. Serrels, et al., “Nuclear FAK controls chemokine transcription, Tregs, and evasion of anti-tumor immunity,” Cell 163, no. 1 (2015): 160–173.

[311]

M. Canel, A. Byron, A. H. Sims, J. Cartier, H. Patel, and M. C. Frame, “Nuclear FAK and Runx1 Cooperate to Regulate IGFBP3, Cell-Cycle Progression, and Tumor Growth,” Cancer Research 77, no. 19 (2017): 5301–5312.

[312]

B. Serrels, N. McGivern, M. Canel, A. Byron, S. C. Johnson, and H. J. McSorley, “IL-33 and ST2 mediate FAK-dependent antitumor immune evasion Through transcriptional networks,” Science Signaling 10, no. 508 (2017).

[313]

P. S. Thiagarajan, M. Sinyuk, S. M. Turaga, et al., “Cx26 drives self-renewal in triple-negative breast cancer via interaction With NANOG and focal adhesion kinase,” Nature Communications 9, no. 1 (2018): 578.

[314]

J. B. Heim, E. J. Squirewell, A. Neu, et al., “Myosin-1E interacts With FAK proline-rich region 1 to induce fibronectin-type matrix,” PNAS 114, no. 15 (2017): 3933–3938.

[315]

S. T. Lim, N. L. Miller, X. L. Chen, et al., “Nuclear-localized focal adhesion kinase regulates inflammatory VCAM-1 expression,” Journal of Cell Biology 197, no. 7 (2012): 907–919.

[316]

A. R. Pedrosa, N. Bodrug, J. Gomez-Escudero, et al., “Tumor Angiogenesis Is Differentially Regulated by Phosphorylation of Endothelial Cell Focal Adhesion Kinase Tyrosines-397 and -861,” Cancer Research 79, no. 17 (2019): 4371–4386.

[317]

C. Jean, X. L. Chen, J. O. Nam, et al., “Inhibition of endothelial FAK activity prevents tumor metastasis by enhancing barrier function,” Journal of Cell Biology 204, no. 2 (2014): 247–263.

[318]

H. Jiang, S. Hegde, B. L. Knolhoff, et al., “Targeting focal adhesion kinase renders pancreatic cancers responsive to checkpoint immunotherapy,” Nature Medicine 22, no. 8 (2016): 851–860.

[319]

M. J. Mitchell and M. R. King, “Computational and experimental models of cancer cell response to fluid shear stress,” Frontiers in Oncology 3 (2013): 44.

[320]

B. Xuan, D. Ghosh, E. M. Cheney, E. M. Clifton, and M. R. Dawson, “Dysregulation in Actin Cytoskeletal Organization Drives Increased Stiffness and Migratory Persistence in Polyploidal Giant Cancer Cells,” Scientific Reports 8, no. 1 (2018): 11935.

[321]

M. P. Girouard, M. Pool, R. Alchini, I. Rambaldi, and A. E. Fournier, “RhoA Proteolysis Regulates the Actin Cytoskeleton in Response to Oxidative Stress,” PLoS ONE 11, no. 12 (2016): e0168641.

[322]

S. Mostowy and P. Cossart, “Septins: The fourth component of the cytoskeleton,” Nature Reviews Molecular Cell Biology 13, no. 3 (2012): 183–194.

[323]

Y. Zeng, Y. Cao, L. Liu, et al., “SEPT9_i1 regulates human breast cancer cell motility Through cytoskeletal and RhoA/FAK signaling pathway regulation,” Cell Death & Disease 10, no. 10 (2019): 720.

[324]

J. J. Manfredi and S. B. Horwitz, “Taxol: An antimitotic agent With a new mechanism of action,” Pharmacology & Therapeutics 25, no. 1 (1984): 83–125.

[325]

M. Tello-Lafoz, K. Srpan, E. E. Sanchez, et al., “Cytotoxic lymphocytes target characteristic biophysical vulnerabilities in cancer,” Immunity 54, no. 5 (2021): 1037–1054.e7.

[326]

S. Park, M. J. Colville, C. R. Shurer, et al., “Mucins form a nanoscale material barrier Against immune cell attack,” BioRxiv (2022). 2022.01.28.478211.

[327]

Y. Wu, Y. Song, J. Soto, et al., “Viscoelastic extracellular matrix enhances epigenetic remodeling and cellular plasticity,” Nature Communications 16, no. 1 (2025): 4054.

[328]

S. M. Wilk, K. Lee, C. C. Castillo, et al., “Multiplex imaging reveals novel patterns of MRTFA/B activation in the breast cancer microenvironment,” Journal of Translational Medicine 23, no. 1 (2025): 599.

[329]

T. A. Wynn and T. R. Ramalingam, “Mechanisms of fibrosis: Therapeutic translation for fibrotic disease,” Nature Medicine 18, no. 7 (2012): 1028–1040.

[330]

N. C. Henderson, F. Rieder, and T. A. Wynn, “Fibrosis: From mechanisms to medicines,” Nature 587, no. 7835 (2020): 555–566.

[331]

S. Mascharak, J. L. Guo, M. Griffin, C. E. Berry, D. C. Wan, and M. T. Longaker, “Modelling and targeting mechanical forces in organ fibrosis,” Nature Reviews Bioengineering 2, no. 4 (2024): 305–323.

[332]

H. Chen, J. Qu, X. Huang, et al., “Mechanosensing by the α6-integrin confers an invasive fibroblast phenotype and mediates lung fibrosis,” Nature Communications 7 (2016): 12564.

[333]

G. S. Horan, S. Wood, V. Ona, et al., “Partial Inhibition of Integrin αvβ6 Prevents Pulmonary Fibrosis Without Exacerbating Inflammation,” American Journal of Respiratory and Critical Care Medicine 177, no. 1 (2008): 56–65.

[334]

K. K. Kim, Y. Wei, C. Szekeres, et al., “Epithelial cell alpha3beta1 integrin links beta-catenin and Smad signaling to promote myofibroblast formation and pulmonary fibrosis,” Journal of Clinical Investigation 119, no. 1 (2009): 213–224.

[335]

Y. Chang, W. L. Lau, H. Jo, et al., “Pharmacologic Blockade of αvβ1 Integrin Ameliorates Renal Failure and Fibrosis In Vivo,” Journal of the American Society of Nephrology 28, no. 7 (2017): 1998–2005.

[336]

N. C. Henderson, T. D. Arnold, Y. Katamura, et al., “Targeting of αv integrin identifies a core molecular pathway that regulates fibrosis in several organs,” Nature Medicine 19, no. 12 (2013): 1617–1624.

[337]

V. W. Wong, K. C. Rustad, S. Akaishi, et al., “Focal adhesion kinase links mechanical force to skin fibrosis via inflammatory signaling,” Nature Medicine 18, no. 1 (2011): 148–152.

[338]

D. Lagares, O. Busnadiego, R. A. García-Fernández, et al., “Inhibition of focal adhesion kinase prevents experimental lung fibrosis and myofibroblast formation,” Arthritis and Rheumatism 64, no. 5 (2012): 1653–1664.

[339]

Y. Watanabe, M. Tamura, A. Osajima, et al., “Integrins induce expression of monocyte chemoattractant protein-1 via focal adhesion kinase in mesangial cells,” Kidney International 64, no. 2 (2003): 431–440.

[340]

Y. Zhou, X. Huang, L. Hecker, et al., “Inhibition of mechanosensitive signaling in myofibroblasts ameliorates experimental pulmonary fibrosis,” Journal of Clinical Investigation 123, no. 3 (2013): 1096–1108.

[341]

C. Dou, Z. Liu, K. Tu, et al., “P300 Acetyltransferase Mediates Stiffness-Induced Activation of Hepatic Stellate Cells Into Tumor-Promoting Myofibroblasts,” Gastroenterology 154, no. 8 (2018): 2209–2221.e14.

[342]

S. S. Desai, J. C. Tung, V. X. Zhou, et al., “Physiological ranges of matrix rigidity modulate primary mouse hepatocyte function in part Through hepatocyte nuclear factor 4 alpha,” Hepatology 64, no. 1 (2016): 261–275.

[343]

S. Tada, H. Iwamoto, M. Nakamuta, et al., “A selective ROCK inhibitor, Y27632, prevents dimethylnitrosamine-induced hepatic fibrosis in rats,” Journal of Hepatology 34, no. 4 (2001): 529–536.

[344]

J. M. Carbajal, M. L. Gratrix, C.-H. Yu, and R. C. Schaeffer, “ROCK mediates thrombin's endothelial barrier dysfunction,” American Journal of Physiology-Cell Physiology 279, no. 1 (2000): C195–C204.

[345]

D. A. Simonetto, H. Y. Yang, M. Yin, et al., “Chronic passive venous congestion drives hepatic fibrogenesis via sinusoidal thrombosis and mechanical forces,” Hepatology 61, no. 2 (2015): 648–659.

[346]

M. A. Chapman, J. Zhang, I. Banerjee, et al., “Disruption of both nesprin 1 and desmin results in nuclear anchorage defects and fibrosis in skeletal muscle,” Human Molecular Genetics 23, no. 22 (2014): 5879–5892.

[347]

B. Bourgeois, B. Gilquin, C. Tellier-Lebègue, et al., “Inhibition of TGF-β signaling at the nuclear envelope: Characterization of interactions Between MAN1, Smad2 and Smad3, and PPM1A,” Science signaling 6, no. 280 (2013): ra49.

[348]

C. Y. Ho, D. E. Jaalouk, M. K. Vartiainen, and J. Lammerding, “Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics,” Nature 497, no. 7450 (2013): 507–511.

[349]

S. Mascharak, H. E. desJardins-Park, M. F. Davitt, et al., “Preventing Engrailed-1 activation in fibroblasts yields wound regeneration Without scarring,” Science 372, no. 6540 (2021).

[350]

K. Martin, J. Pritchett, J. Llewellyn, et al., “PAK proteins and YAP-1 signalling downstream of integrin beta-1 in myofibroblasts promote liver fibrosis,” Nature Communications 7 (2016): 12502.

[351]

F. Liu, D. Lagares, K. M. Choi, et al., “Mechanosignaling Through YAP and TAZ drives fibroblast activation and fibrosis,” American Journal of Physiology. Lung Cellular and Molecular Physiology 308, no. 4 (2015): L344–L357.

[352]

T. H. Sisson, I. O. Ajayi, N. Subbotina, et al., “Inhibition of myocardin-related transcription factor/serum response factor signaling decreases lung fibrosis and promotes mesenchymal cell apoptosis,” American Journal of Pathology 185, no. 4 (2015): 969–986.

[353]

N. Sakai, J. Chun, J. S. Duffield, T. Wada, A. D. Luster, and A. M. Tager, “LPA1-induced cytoskeleton reorganization drives fibrosis Through CTGF-dependent fibroblast proliferation,” Faseb Journal 27, no. 5 (2013): 1830–1846.

[354]

C.-M. Horejs, A. Serio, A. Purvis, et al., “Biologically-active laminin-111 fragment that modulates the epithelial-to-mesenchymal transition in embryonic stem cells,” Proceedings of the National Academy of Sciences 111, no. 16 (2014): 5908–5913.

[355]

B. C. Capell and F. S. Collins, “Human laminopathies: Nuclei gone genetically awry,” Nature Reviews Genetics 7, no. 12 (2006): 940–952.

[356]

Q. Hu, E. J. Moerman, and S. Goldstein, “Altered Expression and Regulation of the α5β1 Integrin–Fibronectin Receptor Lead to Reduced Amounts of Functional α5β1 Heterodimer on the Plasma Membrane of Senescent Human Diploid Fibroblasts,” Experimental Cell Research 224, no. 2 (1996): 251–263.

[357]

M. J. Reed, N. S. Ferara, and R. B. Vernon, “Impaired migration, integrin function, and actin cytoskeletal organization in dermal fibroblasts From a subset of aged human donors,” Mechanisms of Ageing and Development 122, no. 11 (2001): 1203–1220.

[358]

M. Shakibaei, H. Abou-Rebyeh, and H. J. Merker, “Integrins in ageing cartilage tissue in vitro,” Histology and Histopathology 8, no. 4 (1993): 715–723.

[359]

V. Rapisarda, M. Borghesan, V. Miguela, et al., “Integrin Beta 3 Regulates Cellular Senescence by Activating the TGF-β Pathway,” Cell Reports 18, no. 10 (2017): 2480–2493.

[360]

E. Y. Shin, J. H. Park, S. T. You, et al., “Integrin-mediated adhesions in regulation of cellular senescence,” Science Advances 6, no. 19 (2020): eaay3909.

[361]

K. A. Cho, S. J. Ryu, Y. S. Oh, et al., “Morphological adjustment of senescent cells by modulating caveolin-1 status,” Journal of Biological Chemistry 279, no. 40 (2004): 42270–42278.

[362]

R. Aikawa, T. Nagai, S. Kudoh, et al., “Integrins Play a Critical Role in Mechanical Stress–Induced p38 MAPK Activation,” Hypertension 39, no. 2 (2002): 233–238.

[363]

K. M. Rice, D. H. Desai, R. S. Kinnard, R. Harris, G. L. Wright, and E. R. Blough, “Load-induced focal adhesion mechanotransduction is altered With aging in the Fischer 344/NNiaHSd × Brown Norway/BiNia rat aorta,” Biogerontology 8, no. 3 (2007): 257–267.

[364]

K. Nishio and A. Inoue, “Senescence-associated alterations of cytoskeleton: Extraordinary production of vimentin that anchors cytoplasmic p53 in senescent human fibroblasts,” Histochemistry and Cell Biology 123, no. 3 (2005): 263–273.

[365]

J. W. Seawright, H. Sreenivasappa, H. C. Gibbs, et al., “Vascular Smooth Muscle Contractile Function Declines With Age in Skeletal Muscle Feed Arteries,” Frontiers in Physiology 9 (2018): 856.

[366]

G. G. Garcia, A. A. Sadighi Akha, and R. A. Miller, “Age-related defects in moesin/ezrin cytoskeletal signals in mouse CD4 T cells,” Journal of Immunology 179, no. 10 (2007): 6403–6409.

[367]

K. H. Chang, R. C. Nayak, S. Roy, et al., “Vasculopathy-associated hyperangiotensinemia mobilizes haematopoietic stem cells/progenitors Through endothelial AT2R and cytoskeletal dysregulation,” Nature Communications 6 (2015): 5914.

[368]

M. Ohgushi, M. Matsumura, M. Eiraku, et al., “Molecular Pathway and Cell State Responsible for Dissociation-Induced Apoptosis in Human Pluripotent Stem Cells,” Cell Stem Cell 7, no. 2 (2010): 225–239.

[369]

M. Segel, B. Neumann, M. F. E. Hill, et al., “Niche stiffness underlies the ageing of central nervous system progenitor cells,” Nature 573, no. 7772 (2019): 130–134.

[370]

K. M. Rao, M. S. Currie, J. Padmanabhan, and H. J. Cohen, “Age-related alterations in actin cytoskeleton and receptor expression in human leukocytes,” Journal of Gerontology 47, no. 2 (1992): B37–B44.

[371]

G. G. Garcia and R. A. Miller, “Age-related defects in the cytoskeleton signaling pathways of CD4 T cells,” Ageing Research Reviews 10, no. 1 (2011): 26–34.

[372]

Z. Li, Y. Jiao, E. K. Fan, et al., “Aging-Impaired Filamentous Actin Polymerization Signaling Reduces Alveolar Macrophage Phagocytosis of Bacteria,” Journal of Immunology 199, no. 9 (2017): 3176–3186.

[373]

X. Yue, J. Cui, Z. Sun, et al., “Nuclear softening mediated by Sun2 suppression delays mechanical stress-induced cellular senescence,” Cell Death Discovery 9, no. 1 (2023): 167.

[374]

J. Afilalo, I. A. Sebag, L. E. Chalifour, et al., “Age-related changes in lamin A/C expression in cardiomyocytes,” American Journal of Physiology-Heart and Circulatory Physiology 293, no. 3 (2007): H1451–H1456.

[375]

G. Duque and D. Rivas, “Age-related changes in lamin A/C expression in the osteoarticular system: Laminopathies as a potential new aging mechanism,” Mechanisms of Ageing and Development 127, no. 4 (2006): 378–383.

[376]

P. Scaffidi and T. Misteli, “Lamin A-dependent nuclear defects in human aging,” Science 312, no. 5776 (2006): 1059–1063.

[377]

D. K. Shumaker, T. Dechat, A. Kohlmaier, et al., “Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging,” PNAS 103, no. 23 (2006): 8703–8708.

[378]

A. D. Stephens, P. Z. Liu, E. J. Banigan, et al., “Chromatin histone modifications and rigidity affect nuclear morphology independent of lamins,” Molecular Biology of the Cell 29, no. 2 (2018): 220–233.

[379]

T. D. Nguyen, M. K. Rao, S. P. Dhyani, et al., “Nucleoporin93 limits Yap activity to prevent endothelial cell senescence,” Aging Cell 23, no. 4 (2024): e14095.

[380]

F. A. Pelissier, J. C. Garbe, B. Ananthanarayanan, et al., “Age-related dysfunction in mechanotransduction impairs differentiation of human mammary epithelial progenitors,” Cell Reports 7, no. 6 (2014): 1926–1939.

[381]

T. Mammoto, Y. S. Torisawa, M. Muyleart, et al., “Effects of age-dependent changes in cell size on endothelial cell proliferation and senescence Through YAP1,” Aging (Albany NY) 11, no. 17 (2019): 7051–7069.

[382]

K. M. Stearns-Reider, A. D'Amore, K. Beezhold, B. Rothrauff, L. Cavalli, and W. R. Wagner, “Aging of the skeletal muscle extracellular matrix drives a stem cell fibrogenic conversion,” Aging Cell 16, no. 3 (2017): 518–528.

[383]

K. Sakuma, M. Akiho, H. Nakashima, H. Akima, and M. Yasuhara, “Age-related reductions in expression of serum response factor and myocardin-related transcription factor A in mouse skeletal muscles,” Biochimica Et Biophysica Acta (BBA)—Molecular Basis of Disease 1782, no. 7 (2008): 453–461.

[384]

H. L. Sladitschek-Martens, A. Guarnieri, G. Brumana, et al., “YAP/TAZ activity in stromal cells prevents ageing by controlling cGAS–STING,” Nature 607, no. 7920 (2022): 790–798.

[385]

X. Pang, X. He, Z. Qiu, et al., “Targeting integrin pathways: Mechanisms and advances in therapy,” Signal Transduction and Targeted Therapy 8, no. 1 (2023): 1.

[386]

R. J. Slack, S. J. F. Macdonald, J. A. Roper, R. G. Jenkins, and R. J. D. Hatley, “Emerging therapeutic opportunities for integrin inhibitors,” Nature Reviews Drug Discovery 21, no. 1 (2022): 60–78.

[387]

J. Gao, J. Cheng, W. Xie, et al., “Prospects of focal adhesion kinase inhibitors as a cancer therapy in preclinical and early phase study,” Expert Opinion on Investigational Drugs 33, no. 6 (2024): 639–651.

[388]

H. H. Hu, S. Q. Wang, H. L. Shang, et al., “Roles and inhibitors of FAK in cancer: Current advances and future directions,” Frontiers in Pharmacology 15 (2024): 1274209.

[389]

X. Shang, F. Marchioni, N. Sipes, et al., “Rational design of small molecule inhibitors targeting RhoA subfamily Rho GTPases,” Chemistry & Biology 19, no. 6 (2012): 699–710.

[390]

X. Shang, F. Marchioni, C. R. Evelyn, et al., “Small-molecule inhibitors targeting G-protein–coupled Rho guanine nucleotide exchange factors,” Proceedings of the National Academy of Sciences 110, no. 8 (2013): 3155–3160.

[391]

M. Vogelsgesang, A. Pautsch, and K. Aktories, “C3 exoenzymes, novel insights Into structure and action of Rho-ADP-ribosylating toxins,” Naunyn-Schmiedebergs Archives of Pharmacology 374, no. 5-6 (2007): 347–360.

[392]

R. A. Dee, K. D. Mangum, X. Bai, C. P. Mack, and J. M. Taylor, “Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure,” Pharmacology & Therapeutics 193 (2019): 121–134.

[393]

C. R. Evelyn, S. M. Wade, Q. Wang, et al., “CCG-1423: A small-molecule inhibitor of RhoA transcriptional signaling,” Molecular Cancer Therapeutics 6, no. 8 (2007): 2249–2260.

[394]

J. L. Bell, A. J. Haak, S. M. Wade, P. D. Kirchhoff, R. R. Neubig, and S. D. Larsen, “Optimization of novel nipecotic bis(amide) inhibitors of the Rho/MKL1/SRF transcriptional pathway as potential anti-metastasis agents,” Bioorganic & Medicinal Chemistry Letters 23, no. 13 (2013): 3826–3832.

[395]

C. Yu-Wai-Man, B. Spencer-Dene, R. M. H. Lee, et al., “Local delivery of novel MRTF/SRF inhibitors prevents scar tissue formation in a preclinical model of fibrosis,” Scientific Reports 7, no. 1 (2017): 518.

[396]

K. M. Hutchings, E. M. Lisabeth, W. Rajeswaran, et al., “Pharmacokinetic optimitzation of CCG-203971: Novel inhibitors of the Rho/MRTF/SRF transcriptional pathway as potential antifibrotic therapeutics for systemic scleroderma,” Bioorganic & Medicinal Chemistry Letters 27, no. 8 (2017): 1744–1749.

[397]

M. R. Lundquist, A. J. Storaska, T. C. Liu, et al., “Redox modification of nuclear actin by MICAL-2 regulates SRF signaling,” Cell 156, no. 3 (2014): 563–576.

[398]

J. M. Franklin, Z. Wu, and K.-L. Guan, “Insights Into recent findings and clinical application of YAP and TAZ in cancer,” Nature Reviews Cancer 23, no. 8 (2023): 512–525.

[399]

M. Coué, S. L. Brenner, I. Spector, and E. D. Korn, “Inhibition of actin polymerization by latrunculin A,” Febs Letters 213, no. 2 (1987): 316–318.

[400]

M. D. Flanagan and S. Lin, “Cytochalasins block actin filament elongation by binding to high affinity sites associated With F-actin,” Journal of Biological Chemistry 255, no. 3 (1980): 835–838.

[401]

B. J. Nolen, N. Tomasevic, A. Russell, et al., “Characterization of two classes of small molecule inhibitors of Arp2/3 complex,” Nature 460, no. 7258 (2009): 1031–1034.

[402]

R. Ponsaerts, C. D'Hondt, G. Bultynck, S. P. Srinivas, J. Vereecke, and B. Himpens, “The myosin II ATPase inhibitor blebbistatin prevents thrombin-induced inhibition of intercellular calcium wave propagation in corneal endothelial cells,” Investigative Ophthalmology & Visual Science 49, no. 11 (2008): 4816–4827.

[403]

R. Nakamoto, V. Ferri, H. Duan, et al., “Pilot-phase PET/CT study targeting integrin α(v)β(6) in pancreatic cancer patients using the cystine-knot peptide-based (18)F-FP-R(0)1-MG-F2,” European Journal of Nuclear Medicine and Molecular Imaging 50, no. 1 (2022): 184–193.

[404]

J. Klubo-Gwiezdzinska and X. Chen, “Targeting Integrins With Radiolabeled RGD Analogues for Radiotheranostics of Metastatic Radioactive Iodine Nonresponsive Thyroid Cancer: New Avenues in Personalized Medicine,” Thyroid: Official Journal of the American Thyroid Association 30, no. 4 (2020): 476–478.

[405]

R. Sharma, P. O. Valls, M. Inglese, et al., “[(18)F]Fluciclatide PET as a biomarker of response to combination therapy of pazopanib and paclitaxel in platinum-resistant/refractory ovarian cancer,” European Journal of Nuclear Medicine and Molecular Imaging 47, no. 5 (2020): 1239–1251.

[406]

K. S. de Valk, M. M. Deken, H. J. M. Handgraaf, et al., “First-in-Human Assessment of cRGD-ZW800-1, a Zwitterionic, Integrin-Targeted, Near-Infrared Fluorescent Peptide in Colon Carcinoma,” Clinical Cancer Research 26, no. 15 (2020): 3990–3998.

[407]

D. Kegyes, C. Constantinescu, L. Vrancken, et al., “Patient selection for CAR T or BiTE therapy in multiple myeloma: Which treatment for each patient?,” Journal of Hematology & Oncology 15, no. 1 (2022): 78.

[408]

I. Petrini, M. Sollini, F. Bartoli, et al., “ED-B-Containing Isoform of Fibronectin in Tumor Microenvironment of Thymomas: A Target for a Theragnostic Approach,” Cancers (Basel) 14, no. 11 (2022).

[409]

T. Li, G. Ge, H. Zhang, et al., “HM-3-HSA exhibits potent anti-angiogenesis and antitumor activity in hepatocellular carcinoma,” European Journal of Pharmaceutical Sciences 167 (2021): 106017.

[410]

N. Lu, T. Ji, Y. Lu, X. Xu, X. Gu, and Y. Ding, “Drug delivery strategies and clinical research progress for encephalopathy,” Journal of China Pharmaceutical University 55, no. 5 (2024): 577–589.

[411]

C. Bergonzini, K. Kroese, A. J. M. Zweemer, and E. H. J. Danen, “Targeting Integrins for Cancer Therapy—Disappointments and Opportunities,” Frontiers in Cell and Developmental Biology 10 (2022): 863850.

[412]

X. Pang, X. He, Z. Qiu, et al., “Targeting integrin pathways: Mechanisms and advances in therapy,” Signal Transduction and Targeted Therapy 8, no. 1 (2023): 1.

[413]

H. A. Ogana, S. Hurwitz, N. Wei, et al., “Targeting integrins in drug-resistant acute myeloid leukaemia,” British Journal of Pharmacology 181, no. 2 (2024): 295–316.

[414]

R. Newhouse, E. Nelissen, K. H. El-Shakankery, et al., “Pegylated liposomal doxorubicin for relapsed epithelial ovarian cancer,” Cochrane Database of Systematic Reviews (Online) 7, no. 7 (2023): Cd006910.

[415]

B. Besse, L. C. Tsao, D. T. Chao, et al., “Phase Ib safety and pharmacokinetic study of volociximab, an anti-α5β1 integrin antibody, in combination With carboplatin and paclitaxel in advanced non-small-cell lung cancer,” Annals of Oncology 24, no. 1 (2013): 90–96.

[416]

Z. Gu, Y. Du, X. Zhao, and C. Wang, “Tumor microenvironment and metabolic remodeling in gemcitabine-based chemoresistance of pancreatic cancer,” Cancer Letters 521 (2021): 98–108.

[417]

X. Tan, Y. Yan, B. Song, S. Zhu, Q. Mei, and K. Wu, “Focal adhesion kinase: From biological functions to therapeutic strategies,” Experimental Hematology & Oncology 12, no. 1 (2023): 83.

[418]

T. Shimizu, K. Fukuoka, M. Takeda, et al., “A first-in-Asian phase 1 study to evaluate safety, pharmacokinetics and clinical activity of VS-6063, a focal adhesion kinase (FAK) inhibitor in Japanese patients With advanced solid tumors,” Cancer Chemotheraphy and Pharmacology 77, no. 5 (2016): 997–1003.

[419]

S. F. Jones, L. L. Siu, J. C. Bendell, et al., “A phase I study of VS-6063, a second-generation focal adhesion kinase inhibitor, in patients With advanced solid tumors,” Investigational New Drugs 33, no. 5 (2015): 1100–1107.

[420]

K. Masuda, H. Ishiki, S. Oyamada, M. Shimizu, D. Kiuchi, and E. Satomi, “Questions Regarding the Randomized Phase II Trial of Defactinib as Maintenance Therapy in Malignant Pleural Mesothelioma,” Journal of Clinical Oncology 37, no. 25 (2019): 2293–2294.

[421]

P. K. Brastianos, E. L. Twohy, E. R. Gerstner, et al., “Alliance A071401: Phase II Trial of Focal Adhesion Kinase Inhibition in Meningiomas With Somatic NF2 Mutations,” Journal of Clinical Oncology 41, no. 3 (2023): 618–628.

[422]

J. C. Soria, H. K. Gan, S. P. Blagden, et al., “A phase I, pharmacokinetic and pharmacodynamic study of GSK2256098, a focal adhesion kinase inhibitor, in patients With advanced solid tumors,” Annals of Oncology 27, no. 12 (2016): 2268–2274.

[423]

M. Yang, H. Xiang, and G. Luo, “Targeting focal adhesion kinase (FAK) for cancer therapy: FAK inhibitors, FAK-based dual-target inhibitors and PROTAC degraders,” Biochemical Pharmacology 224 (2024): 116246.

[424]

Z.-N. Lei, Q.-X. Teng, Q. Tian, et al., “Signaling pathways and therapeutic interventions in gastric cancer,” Signal Transduction and Targeted Therapy 7, no. 1 (2022): 358.

[425]

D. Papadatos-Pastos, R. Kumar, T. A. Yap, et al., “A first-in-human study of the dual ROCK I/II inhibitor, AT13148, in patients With advanced cancers,” Journal of Clinical Oncology 33, no. 15_suppl (2015): 2566.

[426]

S. J. Zhou, J. Wei, S. Su, F. J. Chen, Y. D. Qiu, and B. R. Liu, “Strategies for Bispecific Single Chain Antibody in Cancer Immunotherapy,” Journal of Cancer 8, no. 18 (2017): 3689–3696.

[427]

L. Lv and X. Zhou, “Targeting Hippo signaling in cancer: Novel perspectives and therapeutic potential,” MedComm 4, no. 5 (2023): e375.

[428]

E. A. Chapeau, L. Sansregret, G. G. Galli, et al., “Direct and selective pharmacological disruption of the YAP-TEAD interface by IAG933 inhibits Hippo-dependent and RAS-MAPK-altered cancers,” Nature Cancer 5, no. 7 (2024): 1102–1120.

[429]

L. W. Wu, S. J. Jang, C. Shapiro, et al., “Diffuse Gastric Cancer: A Comprehensive Review of Molecular Features and Emerging Therapeutics,” Targeted Oncology 19, no. 6 (2024): 845–865.

[430]

S. A. Abdel Gaber and M. Fadel, “Nanotechnology and photodynamic therapy From a clinical perspective,” Translational Biophotonics 5, no. 1 (2023): e202200016.

[431]

H. Y. Lai, K. H. Yu, K. C. Tsai, et al., “The first attempt in synthesis, identification, and evaluation of SEPT9 inhibitors on human oral squamous carcinomas,” Bioorganic Chemistry 154 (2025): 108068.

[432]

X. Shang, F. Marchioni, C. R. Evelyn, et al., “Small-molecule inhibitors targeting G-protein-coupled Rho guanine nucleotide exchange factors,” PNAS 110, no. 8 (2013): 3155–3160.

[433]

L. Radnai, E. J. Young, C. Kikuti, et al., “Development of Clinically Viable Non-Muscle Myosin II Small Molecule Inhibitors With Broad Therapeutic Potential,” BioRxiv (2024).

[434]

C. J. Guerriero and O. A. Weisz, “N-WASP inhibitor wiskostatin nonselectively perturbs membrane transport by decreasing cellular ATP levels,” American Journal of Physiology. Cell Physiology 292, no. 4 (2007): C1562–C1566.

[435]

Y. J. Yoon, Y. M. Han, J. Choi, et al., “Benproperine, an ARPC2 inhibitor, suppresses cancer cell migration and tumor metastasis,” Biochemical Pharmacology 163 (2019): 46–59.

[436]

B. Hetrick, M. S. Han, L. A. Helgeson, and B. J. Nolen, “Small molecules CK-666 and CK-869 inhibit actin-related protein 2/3 complex by blocking an activating conformational change,” Chemistry & Biology 20, no. 5 (2013): 701–712.

[437]

M. R. Bubb, A. M. Senderowicz, E. A. Sausville, K. L. Duncan, and E. D. Korn, “Jasplakinolide, a cytotoxic natural product, induces actin polymerization and competitively inhibits the binding of phalloidin to F-actin,” Journal of Biological Chemistry 269, no. 21 (1994): 14869–14871.

[438]

T. Isogai, R. van der Kammen, and M. Innocenti, “SMIFH2 has effects on Formins and p53 that perturb the cell cytoskeleton,” Scientific Reports 5 (2015): 9802.

[439]

K. Hayashi, B. Watanabe, Y. Nakagawa, S. Minami, and T. Morita, “RPEL proteins are the molecular targets for CCG-1423, an inhibitor of Rho signaling,” PLoS ONE 9, no. 2 (2014): e89016.

[440]

B. Xiao, “Mechanisms of mechanotransduction and physiological roles of PIEZO channels,” Nature Reviews Molecular Cell Biology 25, no. 11 (2024): 886–903.

[441]

P. Jin, L. Y. Jan, and Y. N. Jan, “Mechanosensitive Ion Channels: Structural Features Relevant to Mechanotransduction Mechanisms,” Annual Review of Neuroscience 43 (2020): 207–229.

[442]

Z. Vittum, S. Cocchiaro, and S. A. Mensah, “Basal endothelial glycocalyx's response to shear stress: A review of structure, function, and clinical implications,” Frontiers in Cell and Developmental Biology 12 (2024): 1371769.

[443]

H. Askari, M. Sadeghinejad, and I. S. Fancher, “Chapter Three—Mechanotransduction and the endothelial glycocalyx: Interactions With membrane and cytoskeletal proteins to transduce force. In: I. S. Fancher and A. Z. Chignalia, editors. Current Topics in Membranes” (Academic Press, 2023): 43–60.

[444]

D. Wachten and P. Mill, “The cilia mechanosensation debate gets (bio)physical,” Nature Reviews Nephrology 19, no. 5 (2023): 279–280.

[445]

E. N. Petersen, H.-W. Chung, A. Nayebosadri, and S. B. Hansen, “Kinetic disruption of lipid rafts is a mechanosensor for phospholipase D,” Nature Communications 7, no. 1 (2016): 13873.

[446]

A. J. Iliff and X. Z. S. Xu, “A Mechanosensitive GPCR that Detects the Bloody Force,” Cell 173, no. 3 (2018): 542–544.

[447]

R. K. Das, V. Gocheva, R. Hammink, O. F. Zouani, and A. E. Rowan, “Stress-stiffening-mediated stem-cell commitment switch in soft responsive hydrogels,” Nature Materials 15, no. 3 (2016): 318–325.

[448]

O. Chaudhuri, L. Gu, M. Darnell, et al., “Substrate stress relaxation regulates cell spreading,” Nature Communications 6, no. 1 (2015): 6365.

[449]

A. Elosegui-Artola, I. Andreu, A. E. M. Beedle, et al., “Force Triggers YAP Nuclear Entry by Regulating Transport Across Nuclear Pores,” Cell 171, no. 6 (2017): 1397–1410.e14.

[450]

P. Martin, C. Pardo-Pastor, R. G. Jenkins, and J. Rosenblatt, “Imperfect wound healing sets the stage for chronic diseases,” Science 386, no. 6726 (2024): eadp2974.

[451]

D. Hanahan, “Hallmarks of Cancer: New Dimensions,” Cancer Discovery 12, no. 1 (2022): 31–46.

[452]

A. Ajoolabady, D. Pratico, S. Bahijri, J. Tuomilehto, V. N. Uversky, and J. Ren, “Hallmarks of cellular senescence: Biology, mechanisms, regulations,” Experimental & Molecular Medicine 57, no. 7 (2025): 1482–1491.

[453]

A. Calcinotto, J. Kohli, E. Zagato, L. Pellegrini, M. Demaria, and A. Alimonti, “Cellular Senescence: Aging, Cancer, and Injury,” Physiological Reviews 99, no. 2 (2019): 1047–1078.

[454]

J. Y. Lee and T. Peng, “Convergent evolution of senescent fibroblasts in fibrosis and cancer With aging,” Seminars in Cancer Biology 106-107 (2024): 192–200.

[455]

C. C. Sprenger, S. R. Plymate, and M. J. Reed, “Aging-related alterations in the extracellular matrix modulate the microenvironment and influence tumor progression,” International Journal of Cancer 127, no. 12 (2010): 2739–2748.

[456]

J. Campisi, “Senescent Cells, Tumor Suppression, and Organismal Aging: Good Citizens, Bad Neighbors,” Cell 120, no. 4 (2005): 513–522.

[457]

Y. Lin and Y. Zheng, “Approaches of targeting Rho GTPases in cancer drug discovery,” Expert Opinion on Drug Discovery 10, no. 9 (2015): 991–1010.

[458]

R. S. Kenchappa, L. Radnai, E. J. Young, et al., “MT-125 inhibits non-muscle myosin IIA and IIB and prolongs survival in glioblastoma,” Cell 188, no. 17 (2025): 4622–4639.e19.

RIGHTS & PERMISSIONS

2025 The Author(s). MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, Ltd.

PDF

3

Accesses

0

Citation

Detail

Sections
Recommended

/