Nuclear factor of activated T cells as a driver of tumor progression and a target for precision therapy

Hira Khan , Khushbakhat Alia , Yusra Al Dhaheri , Muhammad Naseem , Rabah Iratni , Edgar Serfling , Khalid Muhammad

Animal Models and Experimental Medicine ›› 2026, Vol. 9 ›› Issue (7) : 1338 -1352.

PDF (2444KB)
Animal Models and Experimental Medicine ›› 2026, Vol. 9 ›› Issue (7) :1338 -1352. DOI: 10.1002/ame2.70251
REVIEW
Nuclear factor of activated T cells as a driver of tumor progression and a target for precision therapy
Author information +
History +
PDF (2444KB)

Abstract

The Nuclear Factor of Activated T Cells (NFAT) family comprises closely related transcription factors. Numerous biological processes including angiogenesis, invasion, migration, proliferation, and cell survival are regulated by the NFAT family. NFATs are overexpressed and have increased transcriptional activity in a variety of human solid tumors and hematological cancers. Beyond tumor cell-intrinsic roles, NFAT has also emerged as an important regulator of the tumor microenvironment (TME), where it can influence immune cell behavior and contribute to mechanisms of immune evasion. The discovery of the multifaceted functions of NFATs has driven the need to further unveil their role in cancer and provide new insights into other potential roles. This review provides a comprehensive narrative synthesis of current molecular and clinical studies, with particular emphasis on how NFAT shapes tumor immune interactions and modulates the TME. By integrating findings across different cancer types, we highlight how NFAT may contribute to both tumor progression and immune regulation. The review concludes by highlighting significant knowledge gaps and recommending future paths for translational and therapeutic research to leverage NFAT signaling as a potential target in precision cancer therapy.

Keywords

cancer progression / immune evasion / nuclear factor of activated T cells (NFAT) / precision cancer therapy / tumor microenvironment (TME)

Cite this article

Download citation ▾
Hira Khan, Khushbakhat Alia, Yusra Al Dhaheri, Muhammad Naseem, Rabah Iratni, Edgar Serfling, Khalid Muhammad. Nuclear factor of activated T cells as a driver of tumor progression and a target for precision therapy. Animal Models and Experimental Medicine, 2026, 9 (7) : 1338-1352 DOI:10.1002/ame2.70251

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Durand DB, Shaw JP, Bush MR, Replogle RE, Belagaje GR, Crabtree GR. Characterization of antigen receptor response elements within the Interleukin-2 enhancer. Mol Cell Biol. 1988; 8(4): 1715-1724.

[2]

Serfling E, Barthelmäs R, Pfeuffer I, et al. Ubiquitous and lymphocyte-specific factors are involved in the induction of the mouse interleukin 2 gene in T lymphocytes. EMBO J. 1989; 8(2): 465-473.

[3]

Randak C, Brabletz T, Hergenröther M, Sobotta I, Serfling E. Cyclosporin A suppresses the expression of the interleukin 2 gene by inhibiting the binding of lymphocyte-specific factors to the IL-2 enhancer. EMBO J. 1990; 9(8): 2529-2536.

[4]

Sen R, Baltimore D. Inducibility of κimmunoglobulin enhancer-binding protein NF-κB by a posttranslational mechanism. Cell. 1986; 47(6): 921-928.

[5]

Brabletz T, Pietrowski I, Serfling E. The immunosuppressives FK 506 and cyclosporin A inhibit the generation of protein factors binding to the two purine boxes of the interleukin 2 enhancer. Nucleic Acids Res. 1991; 19(1): 61-67.

[6]

Cheng M. Hartmann Stahelin (1925–2011) and the contested history of cyclosporin A. Clin Transpl. 2013; 27(3): 326-329.

[7]

Morris PJ. Comment on Hartman Stahelin (1925–2011) and the contested history of cyclosporine A. Clin Transpl. 2013; 27(3):325.

[8]

Kolata G. Drug transforms transplant medicine. Science. 1983; 221(4605): 40-42.

[9]

O'Keefe SJ, Tamura J, Kincaid RL, Tocci MJ, O'Neill EA. FK-506- and CsA-sensitive activation of the interleukin-2 promoter by calcineurin. Nature. 1992; 357(6380): 692-694.

[10]

Clipstone NA, Crabtree GR. Identification of calcineurin as a key signalling enzyme in T-lymphocyte activation. Nature. 1992; 357(6380): 695-697.

[11]

Liu J, Farmer JD, Lane WS, Friedman J, Weissman I, Schreiber SL. Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes. Cell. 1991; 66(4): 807-815.

[12]

Rao A. Signaling to gene expression: calcium, calcineurin and NFAT. Nat Immunol. 2009; 10(1): 3-5.

[13]

McCaffrey PG, Luo C, Kerppola TK, et al. Isolation of the cyclosporin-sensitive T cell transcription factor NFATp. Science. 1993; 262(5134): 750-754.

[14]

Northrop JP, Ho SN, Chen L, et al. NF-AT components define a family of transcription factors targeted in T-cell activation. Nature. 1994; 369(6480): 497-502.

[15]

McCaffrey PG, Goldfeld AE, Rao A. The role of NFATp in cyclosporin A-sensitive tumor necrosis factor-alpha gene transcription. J Biol Chem. 1994; 269(48): 30445-30450.

[16]

Müller MR, Rao A. NFAT, immunity and cancer: a transcription factor comes of age. Nat Rev Immunol. 2010; 10(9): 645-656.

[17]

Ho SN, Thomas DJ, Timmerman LA, Li X, Francke U, Crabtree GR. NFATc3, a lymphoid-specific NFATc family member that is calcium-regulated and exhibits distinct DNA binding specificity. J Biol Chem. 1995; 270(34): 19898-19907.

[18]

Kader HA, Sabih Ur Rehman S, Saraswathiamma D, et al. NFATc1 deficiency in B cells ameliorates atopic dermatitis. Sci Rep. 2025; 15(1):25170.

[19]

Alrefai H, Muhammad K, Rudolf R, et al. NFATc1 supports imiquimod-induced skin inflammation by suppressing IL-10 synthesis in B cells. Nat Commun. 2016; 7(1):11724.

[20]

Crabtree GR, Olson EN. NFAT signaling: choreographing the social lives of cells. Cell. 2002; 109(2): S67-S79.

[21]

Azeem M, Helal M, Klein-Hessling S, et al. NFATc1 fosters allergic contact dermatitis responses by enhancing the induction of IL-17–producing CD8 cells. J Invest Dermatol. 2025; 145(8): 1995-2006.e5.

[22]

Qin JJ, Nag S, Wang W, et al. NFAT as cancer target: Mission possible? Biochim Biophys Acta. 2014; 1846(2): 297-311.

[23]

Mancini M, Toker A. NFAT proteins: emerging roles in cancer progression. Nat Rev Cancer. 2009; 9(11): 810-820.

[24]

Serfling E, Berberich-Siebelt F, Avots A, et al. NFAT and NF-κB factors—the distant relatives. Int J Biochem Cell Biol. 2004; 36(7): 1166-1170.

[25]

Serfling E, Avots A, Klein-Hessling S, Rudolf R, Vaeth M, Berberich-Siebelt F. NFATc1/αA: the other face of NFAT factors in lymphocytes. Cell Commun Signal. 2012; 10(1): 16.

[26]

Pham LV, Tamayo AT, Li C, Bueso-Ramos C, Ford RJ. An epigenetic chromatin remodeling role for NFATc1 in transcriptional regulation of growth and survival genes in diffuse large B-cell lymphomas. Blood. 2010; 116(19): 3899-3906.

[27]

Fu L, Lin-Lee YC, Pham LV, Tamayo A, Yoshimura L, Ford RJ. Constitutive NF-κB and NFAT activation leads to stimulation of the BLyS survival pathway in aggressive B-cell lymphomas. Blood. 2006; 107(11): 4540-4548.

[28]

Pham LV, Tamayo AT, Yoshimura LC, Lin-Lee YC, Ford RJ. Constitutive NF-κB and NFAT activation in aggressive B-cell lymphomas synergistically activates the CD154 gene and maintains lymphoma cell survival. Blood. 2005; 106(12): 3940-3947.

[29]

Buchholz M, Schatz A, Wagner M, et al. Overexpression of c-myc in pancreatic cancer caused by ectopic activation of NFATc1 and the Ca2+/calcineurin signaling pathway. EMBO J. 2006; 25(15): 3714-3724.

[30]

Yoeli-Lerner M, Yiu GK, Rabinovitz I, Erhardt P, Jauliac S, Toker A. Akt blocks breast cancer cell motility and invasion through the transcription factor NFAT. Mol Cell. 2005; 20(4): 539-550.

[31]

Yoeli-Lerner M, Chin YR, Hansen CK, Toker A. Akt/protein kinase B and glycogen synthase kinase-3β signaling pathway regulates cell migration through the NFAT1 transcription factor. Mol Cancer Res. 2009; 7(3): 425-432.

[32]

Lin Y, Song Y, Zhang Y, Shi M, Hou A, Han S. NFAT signaling dysregulation in cancer: emerging roles in cancer stem cells. Biomed Pharmacother. 2023; 165:115167.

[33]

Hoey T. Isolation of two new members of the NFAT gene family and functional characterization of the NFAT proteins. Immunity. 1995; 2:416.

[34]

Masuda ES, Naito Y, Tokumitsu H, et al. NFATx, a novel member of the nuclear factor of activated T cells family that is expressed predominantly in the thymus. Mol Cell Biol. 1995; 15(5): 2697-2706.

[35]

Wolfe SA, Zhou P, Dötsch V, et al. Unusual Rel-like architecture in the DNA-binding domain of the transcription factor NFATc. Nature. 1997; 385(6612): 172-176.

[36]

Avots A, Buttmann M, Chuvpilo S, et al. CBP/p300 integrates Raf/Rac-signaling pathways in the transcriptional induction of NF-ATc during T cell activation. Immunity. 1999; 10(5): 515-524.

[37]

Hogan PG, Chen L, Nardone J, Rao A. Transcriptional regulation by calcium, calcineurin, and NFAT. Genes Dev. 2003; 17(18): 2205-2232.

[38]

Serfling E, Klein-Hessling S, Palmetshofer A, Bopp T, Stassen M, Schmitt E. NFAT transcription factors in control of peripheral T cell tolerance. Eur J Immunol. 2006; 36(11): 2837-2843.

[39]

Serfling E, Chuvpilo S, Liu J, Höfer T, Palmetshofer A. NFATc1 autoregulation: a crucial step for cell-fate determination. Trends Immunol. 2006; 27(10): 461-469.

[40]

Nguyen TN, Kim LJ, Walters RD, et al. The C-terminal region of human NFATc2 binds cJun to synergistically activate interleukin-2 transcription. Mol Immunol. 2010; 47(14): 2314-2322.

[41]

Geil WM, Yen A. Nuclear Raf-1 kinase regulates the CXCR5 promoter by associating with NFATc3 to drive retinoic acid-induced leukemic cell differentiation. FEBS J. 2014; 281(4): 1170-1180.

[42]

Klein-Hessling S, Bopp T, Jha MK, et al. Cyclic AMP-induced chromatin changes support the NFATc-mediated recruitment of GATA-3 to the interleukin 5 promoter. J Biol Chem. 2008; 283(45): 31030-31037.

[43]

Zhu C, Rao K, Xiong H, et al. Activation of the murine Interleukin-12 p40 promoter by functional interactions between NFAT and ICSBP. J Biol Chem. 2003; 278(41): 39372-39382.

[44]

Yang TTC, Chow CW. Transcription cooperation by NFAT·C/EBP composite enhancer complex. J Biol Chem. 2003; 278(18): 15874-15885.

[45]

Yang XY, Wang LH, Chen T, et al. Activation of human T lymphocytes is inhibited by peroxisome proliferator-activated receptor γ (PPARγ) agonists: PPARγ CO-ASSOCIATION WITH TRANSCRIPTION FACTOR NFAT. J Biol Chem. 2000; 275(7): 4541-4544.

[46]

Dai YS, Xu J, Molkentin JD. The DnaJ-related factor Mrj interacts with nuclear factor of activated T cells c3 and mediates transcriptional repression through class II histone deacetylase recruitment. Mol Cell Biol. 2005; 25(22): 9936-9948.

[47]

Wu Y, Borde M, Heissmeyer V, et al. FOXP3 controls regulatory T cell function through cooperation with NFAT. Cell. 2006; 126(2): 375-387.

[48]

Bodor J, Habener JF. Role of transcriptional repressor ICER in cyclic AMP-mediated attenuation of cytokine gene expression in human thymocytes. J Biol Chem. 1998; 273(16): 9544-9551.

[49]

Mognol GP, Carneiro FRG, Robbs BK, Faget DV, Viola JPB. Cell cycle and apoptosis regulation by NFAT transcription factors: new roles for an old player. Cell Death Dis. 2016; 7(4):e2199.

[50]

Kar P, Nelson C, Parekh AB. Selective activation of the transcription factor NFAT1 by calcium microdomains near Ca2+ release-activated Ca2+ (CRAC) channels. J Biol Chem. 2011; 286(17): 14795-14803.

[51]

Medyouf H, Ghysdael J. The calcineurin/NFAT signaling pathway: a NOVEL therapeutic target in leukemia and solid tumors. Cell Cycle. 2008; 7(3): 297-303.

[52]

Khanizadeh S, Shahzamani K, Nakhaie M, Pormohammad A, Talei G, Mirzaei H. Nuclear factor of activated T cells Signalling and viral pathogens: a dynamic cross-talk. Rev Med Virol. 2025; 35(2):e70023.

[53]

Beals CR, Sheridan CM, Turck CW, Gardner P, Crabtree GR. Nuclear export of NF-ATc enhanced by glycogen synthase Kinase-3. Science. 1997; 275(5308): 1930-1933.

[54]

Bhattacharyya S, Deb J, Patra AK, et al. NFATc1 affects mouse splenic B cell function by controlling the calcineurin–NFAT signaling network. J Exp Med. 2011; 208(4): 823-839.

[55]

Miyakawa H, Woo SK, Dahl SC, Handler JS, Kwon HM. Tonicity-responsive enhancer binding protein, a Rel-like protein that stimulates transcription in response to hypertonicity. Proc Natl Acad Sci. 1999; 96(5): 2538-2542.

[56]

Woo S, Lee S, Kwon MH. TonEBP transcriptional activator in the cellular response to increased osmolality. Pflugers Arch Eur J Physiol. 2002; 444(5): 579-585.

[57]

Kim NH, Hong BK, Choi SY, et al. Reactive oxygen species regulate context-dependent inhibition of NFAT5 target genes. Exp Mol Med. 2013; 45(7):e32.

[58]

Sana I, Mantione ME, Angelillo P, Muzio M. Role of NFAT in chronic lymphocytic leukemia and other B-cell malignancies. Front Oncol. 2021; 11.

[59]

Patra AK, Avots A, Zahedi RP, et al. An alternative NFAT-activation pathway mediated by IL-7 is critical for early thymocyte development. Nat Immunol. 2013; 14(2): 127-135.

[60]

Neal JW, Clipstone NA. Glycogen synthase Kinase-3 inhibits the DNA binding activity of NFATc. J Biol Chem. 2001; 276(5): 3666-3673.

[61]

Engelman JA. Targeting PI3K signalling in cancer: opportunities, challenges and limitations. Nat Rev Cancer. 2009; 9(8): 550-562.

[62]

Okamura H, Garcia-Rodriguez C, Martinson H, Qin J, Virshup DM, Rao A. A conserved docking motif for CK1 binding controls the nuclear localization of NFAT1. Mol Cell Biol. 2004; 24(10): 4184-4195.

[63]

Chow CW, Dong C, Flavell RA, Davis RJ. c-Jun NH2-terminal kinase inhibits targeting of the protein phosphatase calcineurin to NFATc1. Mol Cell Biol. 2000; 20(14): 5227-5234.

[64]

Arron JR, Winslow MM, Polleri A, et al. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21. Nature. 2006; 441(7093): 595-600.

[65]

Suanes-Cobos L, Torres-Ramos M, Aguilera-Ventura I, Serrano-Yubero A, Calzado MA. The dual fate of DYRK2 in cancer: balancing the light and dark side of tumorigenesis. Cancer Metastasis Rev. 2026; 45(1): 2.

[66]

Tripathi MK, Deane NG, Zhu J, et al. NFAT transcriptional activity is associated with metastatic capacity in colon cancer. Cancer Res. 2014; 74(23): 6947-6957.

[67]

Song Y, Jiang Y, Tao D, et al. NFAT2-HDAC1 signaling contributes to the malignant phenotype of glioblastoma. Neuro-Oncology. 2020; 22(1): 46-57.

[68]

Qin JJ, Wang W, Voruganti S, Wang H, Zhang WD, Zhang R. Inhibiting NFAT1 for breast cancer therapy: new insights into the mechanism of action of MDM2 inhibitor JapA. Oncotarget. 2015; 6(32): 33106-33119.

[69]

Zhou Z h, Song J w, Li W, et al. The acid-sensing ion channel, ASIC2, promotes invasion and metastasis of colorectal cancer under acidosis by activating the calcineurin/NFAT1 axis. J Exp Clin Cancer Res. 2017; 36(1):130.

[70]

Lang T, Ding X, Kong L, et al. NFATC2 is a novel therapeutic target for colorectal cancer stem cells. Onco Targets Ther. 2018; 11: 6911-6924.

[71]

Xiao ZJ, Liu J, Wang SQ, et al. NFATc2 enhances tumor-initiating phenotypes through the NFATc2/SOX2/ALDH axis in lung adenocarcinoma. elife. 2017; 6:e26733.

[72]

Liu QQ, Li CM, Fu LN, et al. Enterotoxigenic Bacteroides fragilis induces the stemness in colorectal cancer via upregulating histone demethylase JMJD2B. Gut Microbes. 2020; 12(1):1788900.

[73]

Guo K, Jin F. NFAT5 promotes proliferation and migration of lung adenocarcinoma cells in part through regulating AQP5 expression. Biochem Biophys Res Commun. 2015; 465(3): 644-649.

[74]

Remo A, Simeone I, Pancione M, et al. Systems biology analysis reveals NFAT5 as a novel biomarker and master regulator of inflammatory breast cancer. J Transl Med. 2015; 13(1): 138.

[75]

Zhang Y, Wang X. Targeting the Wnt/β-catenin signaling pathway in cancer. J Hematol Oncol. 2020; 13(1): 165.

[76]

Sengupta S, Jana S, Bhattacharyya A. TGF-β-Smad2-dependent activation of CDC 25A plays an important role in cell proliferation through NFAT activation in metastatic breast cancer cells. Cell Signal. 2014; 26(2): 240-252.

[77]

Sengupta S, Jana S, Biswas S, Mandal PK, Bhattacharyya A. Cooperative involvement of NFAT and SnoN mediates transforming growth factor-β (TGF-β) induced EMT in metastatic breast cancer (MDA-MB 231) cells. Clin Exp Metastasis. 2013; 30(8): 1019-1031.

[78]

Foldynová-Trantírková S, Sekyrová P, Tmejová K, et al. Breast cancer-specific mutations in CK1ε inhibit Wnt/β-catenin and activate the Wnt/Rac1/JNK and NFAT pathways to decrease cell adhesion and promote cell migration. Breast Cancer Res. 2010; 12(3):R30.

[79]

Shou J, Jing J, Xie J, et al. Nuclear factor of activated T cells in cancer development and treatment. Cancer Lett. 2015; 361(2): 174-184.

[80]

Jiang Y, Song Y, Wang R, et al. NFAT1-mediated regulation of NDEL1 promotes growth and invasion of glioma stem-like cells. Cancer Res. 2019; 79(10): 2593-2603.

[81]

Lin DC, Zheng SY, Zhang ZG, et al. TRPC3 promotes tumorigenesis of gastric cancer via the CNB2/GSK3β/NFATc2 signaling pathway. Cancer Lett. 2021; 519: 211-225.

[82]

Griesmann H, Ripka S, Pralle M, et al. WNT5A-NFAT signaling mediates resistance to apoptosis in pancreatic cancer. Neoplasia. 2013; 15(1):11-IN9.

[83]

Xie C, Zhu J, Jiang Y, et al. Sulforaphane inhibits the Acquisition of Tobacco Smoke-Induced Lung Cancer Stem Cell-like Properties via the IL-6/ΔNp63α/Notch Axis. Theranostics. 2019; 9(16): 4827-4840.

[84]

Tillé L, Cropp D, Charmoy M, et al. Activation of the transcription factor NFAT5 in the tumor microenvironment enforces CD8+ T cell exhaustion. Nat Immunol. 2023; 24(10): 1645-1653.

[85]

Werneck MBF, Vieira-de-Abreu A, Chammas R, Viola JPB. NFAT1 transcription factor is central in the regulation of tissue microenvironment for tumor metastasis. Cancer Immunol Immunother. 2011; 60(4): 537-546.

[86]

Oestreich KJ, Yoon H, Ahmed R, Boss JM. NFATc1 regulates PD-1 expression upon T cell activation. J Immunol. 2008; 181(7): 4832-4839.

[87]

Lu P, Youngblood BA, Austin JW, et al. Blimp-1 represses CD8 T cell expression of PD-1 using a feed-forward transcriptional circuit during acute viral infection. J Exp Med. 2014; 211(3): 515-527.

[88]

Sen DR, Kaminski J, Barnitz RA, et al. The epigenetic landscape of T cell exhaustion. Science. 2016; 354(6316): 1165-1169.

[89]

Quigley M, Pereyra F, Nilsson B, et al. Transcriptional analysis of HIV-specific CD8+ T cells shows that PD-1 inhibits T cell function by upregulating BATF. Nat Med. 2010; 16(10): 1147-1151.

[90]

Ma Q, Long W, Xing C, et al. Cancer stem cells and immunosuppressive microenvironment in glioma. Front Immunol. 2018; 9.

[91]

Jiang Y, Han S, Cheng W, Wang Z, Wu A. NFAT1-regulated IL6 signalling contributes to aggressive phenotypes of glioma. Cell Commun Signal. 2017; 15(1):54.

[92]

Tie X, Han S, Meng L, Wang Y, Wu A. NFAT1 is highly expressed in, and regulates the invasion of, glioblastoma multiforme cells. PLoS One. 2013; 8(6):e66008.

[93]

Zhang ZP, Sun XQ, Yuan SJ. APLNR stimulates the development of glioma via the NFAT5/AKT feedback loop. Eur Rev Med Pharmacol Sci. 2020; 24(20): 10594-10600.

[94]

Dittmer J. Breast cancer stem cells: features, key drivers and treatment options. Semin Cancer Biol. 2018; 53: 59-74.

[95]

Tran Quang C, Leboucher S, Passaro D, et al. The calcineurin/NFAT pathway is activated in diagnostic breast cancer cases and is essential to survival and metastasis of mammary cancer cells. Cell Death Dis. 2015; 6(2):e1658.

[96]

Yiu GK, Toker A. NFAT induces breast cancer cell invasion by promoting the induction of Cyclooxygenase-2. J Biol Chem. 2006; 281(18): 12210-12217.

[97]

Siamakpour-Reihani S, Caster J, Nepal DB, et al. The role of calcineurin/NFAT in SFRP2 induced angiogenesis—a rationale for breast cancer treatment with the calcineurin inhibitor tacrolimus. PLoS One. 2011; 6(6):e20412.

[98]

Zhao X, Liu J, Feng L, et al. Anti-angiogenic effects of Qingdu granule on breast cancer through inhibiting NFAT signaling pathway. J Ethnopharmacol. 2018; 222: 261-269.

[99]

Katsuno Y, Derynck R. Epithelial plasticity, epithelial-mesenchymal transition, and the TGF-β family. Dev Cell. 2021; 56(6): 726-746.

[100]

Miao Y, Shen Q, Zhang S, et al. Calcium-sensing stromal interaction molecule 2 upregulates nuclear factor of activated T cells 1 and transforming growth factor-β signaling to promote breast cancer metastasis. Breast Cancer Res. 2019; 21(1):99.

[101]

Nio K, Yamashita T, Kaneko S. The evolving concept of liver cancer stem cells. Mol Cancer. 2017; 16(1):4.

[102]

Zhang X, Zhang Z, Cheng J, et al. Transcription factor NFAT1 activates the mdm2 oncogene independent of p53. J Biol Chem. 2012; 287(36): 30468-30476.

[103]

Wang J, Zhang Y, Liu L, et al. NFAT2 overexpression suppresses the malignancy of hepatocellular carcinoma through inducing Egr2 expression. BMC Cancer. 2020; 20(1):966.

[104]

Li Y, Li G, Tao T, et al. The μ-opioid receptor (MOR) promotes tumor initiation in hepatocellular carcinoma. Cancer Lett. 2019; 453: 1-9.

[105]

Wang J, Zhao H, Zheng L, et al. FGF19/SOCE/NFATc2 signaling circuit facilitates the self-renewal of liver cancer stem cells. Theranostics. 2021; 11(10): 5045-5060.

[106]

Ebrahimi N, Afshinpour M, Fakhr SS, et al. Cancer stem cells in colorectal cancer: signaling pathways involved in stemness and therapy resistance. Crit Rev Oncol Hematol. 2023; 182:103920.

[107]

Peuker K, Muff S, Wang J, et al. Epithelial calcineurin controls microbiota-dependent intestinal tumor development. Nat Med. 2016; 22(5): 506-515.

[108]

Yoshimoto S, Morita H, Matsuda M, Katakura Y, Hirata M, Hashimoto S. NFAT5 promotes oral squamous cell carcinoma progression in a hyperosmotic environment. Lab Investig. 2021; 101(1): 38-50.

[109]

Nguyen A, Kim AH, Kang MK, et al. Chronic alcohol exposure promotes cancer stemness and glycolysis in oral/oropharyngeal squamous cell carcinoma cell lines by activating NFAT signaling. Int J Mol Sci. 2022; 23(17): 9779.

[110]

Lee SH, Kieu C, Martin CE, et al. NFATc3 plays an oncogenic role in oral/oropharyngeal squamous cell carcinomas by promoting cancer stemness via expression of OCT4. Oncotarget. 2019; 10(23): 2306-2319.

[111]

Liu J f, Zhao S h, Wu S s. Depleting NFAT1 expression inhibits the ability of invasion and migration of human lung cancer cells. Cancer Cell Int. 2013; 13(1): 41.

[112]

Yu J, Wang S, Zhao W, et al. Mechanistic exploration of cancer stem cell marker voltage-dependent Calcium Channel α2δ1 subunit-mediated chemotherapy resistance in small-cell lung cancer. Clin Cancer Res. 2018; 24(9): 2148-2158.

[113]

Qi H, Yang Z, Dai C, et al. STAT3 activates MSK1-mediated histone H3 phosphorylation to promote NFAT signaling in gastric carcinogenesis. Oncogene. 2020; 9(2):15.

[114]

Ren L, Ren Q, Wang J, et al. miR-199a-3p promotes gastric cancer progression by promoting its stemness potential via DDR2 mediation. Cell Signal. 2023; 106:110636.

[115]

Baumgart S, Glesel E, Singh G, et al. Restricted heterochromatin formation links NFATc2 repressor activity with growth promotion in pancreatic cancer. Gastroenterology. 2012; 142(2): 388-398.e7.

[116]

Köenig A, Linhart T, Schlengemann K, et al. NFAT-induced histone acetylation relay switch promotes c-Myc-dependent growth in pancreatic cancer cells. Gastroenterology. 2010; 138(3): 1189-1199.e2.

[117]

Singh SK, Chen N, Hessmann E, et al. Antithetical NFATc1–Sox2 and p53–miR200 signaling networks govern pancreatic cancer cell plasticity. EMBO J. 2015; 34(4): 517-530.

[118]

Qin JJ, Li X, Wang W, Zi X, Zhang R. Targeting the NFAT1-MDM2-MDMX network inhibits the proliferation and invasion of prostate cancer cells, independent of p53 and androgen. Front Pharmacol. 2017; 8.

[119]

Liu W, Ren D, Xiong W, Jin X, Zhu L. A novel FBW7/NFAT1 axis regulates cancer immunity in sunitinib-resistant renal cancer by inducing PD-L1 expression. J Exp Clin Cancer Res. 2022; 41(1):38.

[120]

Wang G, Wang YZ, Yu Y, Wang JJ. Inhibitory ASIC2-mediated calcineurin/NFAT against colorectal cancer by triterpenoids extracted from Rhus chinensis mill. J Ethnopharmacol. 2019; 235: 255-267.

[121]

Liu X, Pan CG, Luo ZQ. High expression of NFAT2 contributes to carboplatin resistance in lung cancer. Exp Mol Pathol. 2019; 110:104290.

[122]

Meng X, Li Z, Zhou S, Xiao S, Yu P. miR-194 suppresses high glucose-induced non-small cell lung cancer cell progression by targeting NFAT5. Thoracic Cancer. 2019; 10(5): 1051-1059.

[123]

Xin B, Ji KQ, Liu YS, Zhao XD. NFAT overexpression correlates with CA72-4 and poor prognosis of ovarian clear-cell carcinoma subtype. Reprod Sci. 2021; 28(3): 745-756.

[124]

Caballero FJ, Soler-Torronteras R, Lara-Chica M, et al. AM404 inhibits NFAT and NF-κB signaling pathways and impairs migration and invasiveness of neuroblastoma cells. Eur J Pharmacol. 2015; 746: 221-232.

[125]

Ma J, Du R, Huang Y, et al. Expression, prognosis and gene regulation network of NFAT transcription factors in non-small cell lung cancer. Pathol Oncol Res. 2021; 27:529240.

[126]

Hasselluhn MC, Schmidt GE, Ellenrieder V, Johnsen SA, Hessmann E. Aberrant NFATc1 signaling counteracts TGFβ-mediated growth arrest and apoptosis induction in pancreatic cancer progression. Cell Death Dis. 2019; 10(6):446.

[127]

Barkley D, Moncada R, Pour M, et al. Cancer cell states recur across tumor types and form specific interactions with the tumor microenvironment. Nat Genet. 2022; 54(8): 1192-1201.

[128]

Lewis SM, Asselin-Labat ML, Nguyen Q, et al. Spatial omics and multiplexed imaging to explore cancer biology. Nat Methods. 2021; 18(9): 997-1012.

[129]

Zhong Z, Hou J, Yao Z, et al. Domain generalization enables general cancer cell annotation in single-cell and spatial transcriptomics. Nat Commun. 2024; 15(1): 1929.

[130]

De Zuani M, Xue H, Park JS, et al. Single-cell and spatial transcriptomics analysis of non-small cell lung cancer. Nat Commun. 2024; 15(1):4388.

[131]

Zhang Q, Abdo R, Iosef C, et al. The spatial transcriptomic landscape of non-small cell lung cancer brain metastasis. Nat Commun. 2022; 13(1):5983.

[132]

Heide T, Househam J, Cresswell GD, et al. The co-evolution of the genome and epigenome in colorectal cancer. Nature. 2022; 611(7937): 733-743.

[133]

Yang S, Zhang D, Sun Q, et al. Single-cell and spatial transcriptome profiling identifies the transcription factor BHLHE40 as a driver of EMT in metastatic colorectal cancer. Cancer Res. 2024; 84(13): 2202-2217.

[134]

Wang F, Long J, Li L, et al. Single-cell and spatial transcriptome analysis reveals the cellular heterogeneity of liver metastatic colorectal cancer. Sci Adv. 2023; 9(24):eadf5464.

[135]

Sun C, Wang A, Zhou Y, et al. Spatially resolved multi-omics highlights cell-specific metabolic remodeling and interactions in gastric cancer. Nat Commun. 2023; 14(1):2692.

Rights & permissions

2026 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.

PDF (2444KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/

〈 〉