Volume 45 Issue 6
Jun.  2024
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ZHU Hongyuan, WANG Yushuai, LIN Min. The Mechanochemical Coupling Mechanism of Matrix Stiffnesses and Growth Factors Driving the Epithelial-Mesenchymal Transition[J]. Applied Mathematics and Mechanics, 2024, 45(6): 719-734. doi: 10.21656/1000-0887.450107
Citation: ZHU Hongyuan, WANG Yushuai, LIN Min. The Mechanochemical Coupling Mechanism of Matrix Stiffnesses and Growth Factors Driving the Epithelial-Mesenchymal Transition[J]. Applied Mathematics and Mechanics, 2024, 45(6): 719-734. doi: 10.21656/1000-0887.450107

The Mechanochemical Coupling Mechanism of Matrix Stiffnesses and Growth Factors Driving the Epithelial-Mesenchymal Transition

doi: 10.21656/1000-0887.450107
  • Received Date: 2024-04-19
  • Rev Recd Date: 2024-05-06
  • Publish Date: 2024-06-01
  • The epithelial-mesenchymal transition (EMT) is a critical step in physiological and pathological processes such as the embryonic development, the wound healing, and the cancer progression, wherein cells transition from a tightly adherent epithelial state to a dispersed mesenchymal state. An EMT core circuit model driven by the synergistic regulation of matrix stiffnesses and growth factors was proposed. The results show that, during the EMT, the matrix stiffnesses and growth factors collaboratively regulate the expression of the E/N-cadherin, a typical cell-cell adhesion molecule, by modulating the EMT-activating transcription factors, thus influencing the progression and reversibility of the EMT. The model elucidates the mechanism of synergistic interactions between mechanical and chemical factors on cell-cell adhesion during the EMT, laying a theoretical foundation for understanding the occurrence, development mechanisms, and preventive strategies against diseases such as cancer.

  • (Contributed by LIN Min, M. AMM Editorial Board)
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  • [1]
    NIETO M A, HUANG R Y J, JACKSON R A, et al. EMT: 2016[J]. Cell, 2016, 166(1): 21-45. doi: 10.1016/j.cell.2016.06.028
    [2]
    孙玉川, 李红, 罗庆, 等. 肿瘤组织力学异质性与肿瘤细胞的上皮-间质转化[J]. 医用生物力学, 2021, 36(4): 658-663. https://www.cnki.com.cn/Article/CJFDTOTAL-YISX202104027.htm

    SUN Yuchuan, LI Hong, LUO Qing, et al. Mechanical heterogeneity of tumor tissues and epithelial-mesenchymal transition of tumor cells[J]. Journal of Medical Biomechanics, 2021, 36(4): 658-663. (in Chinese) https://www.cnki.com.cn/Article/CJFDTOTAL-YISX202104027.htm
    [3]
    刘扬, 王金佩, 黄国友, 等. 肿瘤上皮-间质转化(EMT)的生物力学特性研究进展[J]. 西南民族大学学报(自然科学版), 2020, 46(6): 571-577. https://www.cnki.com.cn/Article/CJFDTOTAL-XNMZ202006005.htm

    LIU Yang, WANG Jinpei, HUANG Guoyou, et al. Research advances in biomechanical properties of EMT in tumor cells[J]. Journal of Southwest University for Nationalities (Natural Science Edition), 2020, 46(6): 571-577. (in Chinese) https://www.cnki.com.cn/Article/CJFDTOTAL-XNMZ202006005.htm
    [4]
    FONT-NOGUERA M, MONTEMURRO M, BENASSAYAG C, et al. Getting started for migration: a focus on EMT cellular dynamics and mechanics in developmental models[J]. Cells & Development, 2021, 168: 203717.
    [5]
    THIERY J P, ACLOQUE H, HUANG R Y J, et al. Epithelial-mesenchymal transitions in development and disease[J]. Cell, 2009, 139(5): 871-890. doi: 10.1016/j.cell.2009.11.007
    [6]
    STEMMLER M P, ECCLES R L, BRABLETZ S, et al. Non-redundant functions of EMT transcription factors[J]. Nature Cell Biology, 2019, 21(1): 102-112. doi: 10.1038/s41556-018-0196-y
    [7]
    PUISIEUX A, BRABLETZ T, CARAMEL J. Oncogenic roles of EMT-inducing transcription factors[J]. Nature Cell Biology, 2014, 16(6): 488-494. doi: 10.1038/ncb2976
    [8]
    HAO Y, BAKER D, TEN D P. TGF-β-mediated epithelial-mesenchymal transition and cancer metastasis[J]. International Journal of Molecular Sciences, 2019, 20(11): 2767. doi: 10.3390/ijms20112767
    [9]
    BOARETO M, JOLLY M K, GOLDMAN A, et al. Notch-jagged signalling can give rise to clusters of cells exhibiting a hybrid epithelial/mesenchymal phenotype[J]. Journal of the Royal Society Interface, 2016, 13(118): 20151106. doi: 10.1098/rsif.2015.1106
    [10]
    刘祉宁, 桑晨. 炎性因子引起器官纤维化及上皮-间充质转化机制的研究进展[J]. 生命科学, 2018, 30(8): 868-875. https://www.cnki.com.cn/Article/CJFDTOTAL-SMKX201808010.htm

    LIU Zhining, SANG Chen. Roles of proinflammatory cytokines in organ fibrosis and epithelial-mesenchymal transition[J]. Chinese Bulletin of Life Sciences, 2018, 30(8): 868-875. (in Chinese) https://www.cnki.com.cn/Article/CJFDTOTAL-SMKX201808010.htm
    [11]
    DESPRAT N, SUPATTO W, POUILLE P A, et al. Tissue deformation modulates twist expression to determine anterior midgut differentiation in drosophila embryos[J]. Developmental Cell, 2008, 15(3): 470-477. doi: 10.1016/j.devcel.2008.07.009
    [12]
    张众, XIAO G G S, 石宇, 等. 细胞生命进程中microRNA调控的意义[J]. 临床与实验病理学杂志, 2012, 28(5): 477-481. doi: 10.3969/j.issn.1001-7399.2012.05.001

    ZHANG Zhong, XIAO G G S, SHI Yu, et al. Significance of microRNA regulation in cell life process[J]. Chinese Journal of Clinical and Experimental Pathology, 2012, 28(5): 477-481. (in Chinese) doi: 10.3969/j.issn.1001-7399.2012.05.001
    [13]
    FENG X, WANG Z, FILLMORE R, et al. MiR-200, a new star miRNA in human cancer[J]. Cancer Letters, 2014, 344(2): 166-173. doi: 10.1016/j.canlet.2013.11.004
    [14]
    WELLNER U, SCHUBERT J, BURK U C, et al. The EMT-activator ZEB1 promotes tumorigenicity by repressing stemness-inhibiting microRNAs[J]. Nature Cell Biology, 2009, 11(12): 1487-1495. doi: 10.1038/ncb1998
    [15]
    CHEN L, GIBBONS D L, GOSWAMI S, et al. Metastasis is regulated via microRNA-200/ZEB1 axis control of tumour cell PD-L1 expression and intratumoral immunosuppression[J]. Nature Communications, 2014, 5(1): 5241. doi: 10.1038/ncomms6241
    [16]
    SIEMENS H, JACKSTADT R, HVNTEN S, et al. miR-34 and SNAIL form a double-negative feedback loop to regulate epithelial-mesenchymal transitions[J]. Cell Cycle, 2011, 10(24): 4256-4271. doi: 10.4161/cc.10.24.18552
    [17]
    HAHN S, JACKSTADT R, SIEMENS H, et al. SNAIL and miR-34a feed-forward regulation of ZNF281/ZBP99 promotes epithelial-mesenchymal transition[J]. The EMBO Journal, 2013, 32(23): 3079-3095. doi: 10.1038/emboj.2013.236
    [18]
    GREGORY P A, BRACKEN C P, SMITH E, et al. An autocrine TGF-β/ZEB/miR-200 signaling network regulates establishment and maintenance of epithelial-mesenchymal transition[J]. Molecular Biology of the Cell, 2011, 22(10): 1686-1698. doi: 10.1091/mbc.e11-02-0103
    [19]
    TIAN X J, ZHANG H, XING J. Coupled reversible and irreversible bistable switches underlying TGFβ-induced epithelial to mesenchymal transition[J]. Biophysical Journal, 2013, 105(4): 1079-1089. doi: 10.1016/j.bpj.2013.07.011
    [20]
    ZHANG J, TIAN X J, ZHANG H, et al. TGF-β-induced epithelial-to-mesenchymal transition proceeds through stepwise activation of multiple feedback loops[J]. Science Signaling, 2014, 7(345): ra91.
    [21]
    WEI S C, FATTET L, TSAI J H, et al. Matrix stiffness drives epithelial-mesenchymal transition and tumour metastasis through a TWIST1-G3BP2 mechanotransduction pathway[J]. Nature Cell Biology, 2015, 17(5): 678-688. doi: 10.1038/ncb3157
    [22]
    LEIGHT J L, WOZNIAK M A, CHEN S, et al. Matrix rigidity regulates a switch between TGF-β1-induced apoptosis and epithelial-mesenchymal transition[J]. Molecular Biology of the Cell, 2012, 23(5): 781-791. doi: 10.1091/mbc.e11-06-0537
    [23]
    LU M, JOLLY M K, LEVINE H, et al. MicroRNA-based regulation of epithelial-hybrid-mesenchymal fate determination[J]. Proceedings of the National Academy of Sciences, 2013, 110(45): 18144. doi: 10.1073/pnas.1318192110
    [24]
    TRIPATHI S, CHAKRABORTY P, LEVINE H, et al. A mechanism for epithelial-mesenchymal heterogeneity in a population of cancer cells[J]. PLOS Computational Biology, 2020, 16(2): e1007619. doi: 10.1371/journal.pcbi.1007619
    [25]
    BOCCI F, GEARHART-SERNA L, BOARETO M, et al. Toward understanding cancer stem cell heterogeneity in the tumor microenvironment[J]. Proceedings of the National Academy of Sciences, 2019, 116(1): 148-157. doi: 10.1073/pnas.1815345116
    [26]
    TRIPATHI S, LEVINE H, JOLLY M K. The physics of cellular decision making during epithelial-mesenchymal transition[J]. Annual Review of Biophysics, 2020, 49(1): 1-18. doi: 10.1146/annurev-biophys-121219-081557
    [27]
    PEINADO H, QUINTANILLA M, CANO A. Transforming growth factor β-1 induces snail transcription factor in epithelial cell lines: mechanisms for epithelial mesenchymal transitions[J]. Journal of Biological Chemistry, 2003, 278(23): 21113-21123. doi: 10.1074/jbc.M211304200
    [28]
    DAVE N, GUAITA-ESTERUELAS S, GUTARRA S, et al. Functional cooperation between SNAIL1 and TWIST in the regulation of ZEB1 expression during epithelial to mesenchymal transition[J]. Journal of Biological Chemistry, 2011, 286(14): 12024-12032. doi: 10.1074/jbc.M110.168625
    [29]
    CANO A, PÉREZ-MORENO M A, RODRIGO I, et al. The transcription factor snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression[J]. Nature Cell Biology, 2000, 2(2): 76-83. doi: 10.1038/35000025
    [30]
    BATLLE E, SANCHO E, FRANCÍ C, et al. The transcription factor snail is a repressor of E-cadherin gene expression in epithelial tumour cells[J]. Nature Cell Biology, 2000, 2(2): 84-89. doi: 10.1038/35000034
    [31]
    MORENO-BUENO G, CUBILLO E, SARRIÓ D, et al. Genetic profiling of epithelial cells expressing E-cadherin repressors reveals a distinct role for snail, slug, and E47 factors in epithelial-mesenchymal transition[J]. Cancer Research, 2006, 66(19): 9543-9556. doi: 10.1158/0008-5472.CAN-06-0479
    [32]
    VANDEWALLE C, COMIJN J, DE CRAENE B, et al. SIP1/ZEB2 induces EMT by repressing genes of different epithelial cell-cell junctions[J]. Nucleic Acids Research, 2005, 33(20): 6566-6578. doi: 10.1093/nar/gki965
    [33]
    JIN G, ZHANG Z, WAN J, et al. G3BP2: structure and function[J]. Pharmacological Research, 2022, 186: 106548. doi: 10.1016/j.phrs.2022.106548
    [34]
    FATTET L, JUNG H Y, MATSUMOTO M W, et al. Matrix rigidity controls epithelial-mesenchymal plasticity and tumor metastasis via a mechanoresponsive EPHA2/LYN complex[J]. Developmental Cell, 2020, 54(3): 302-316. doi: 10.1016/j.devcel.2020.05.031
    [35]
    龚博, 林骥, 王彦中, 等. 细胞骨架与细胞外基质的力学建模与分析[J]. 应用数学和力学, 2021, 42(10): 1024-1044. doi: 10.21656/1000-0887.420302

    GONG Bo, LIN Ji, WANG Yanzhong, et al. Mechanical modeling and analyses of cytoskeleton and extracellular matrix[J]. Applied Mathematics and Mechanics, 2021, 42(10): 1024-1044. (in Chinese) doi: 10.21656/1000-0887.420302
    [36]
    CHENG B, WAN W, HUANG G, et al. Nanoscale integrin cluster dynamics controls cellular mechanosensing via FAKY397 phosphorylation[J]. Science Advances, 2020, 6(10): eaax1909. doi: 10.1126/sciadv.aax1909
    [37]
    程波, 徐峰. 考虑细胞外基质黏弹性行为的细胞黏附力学模型[J]. 应用数学和力学, 2021, 42(10): 1074-1080. doi: 10.21656/1000-0887.420259

    CHENG Bo, XU Feng. A molecular clutch model of cellular adhesion on viscoelastic substrate[J]. Applied Mathematics and Mechanics, 2021, 42(10): 1074-1080. (in Chinese) doi: 10.21656/1000-0887.420259
    [38]
    ALEXANDER N R, TRAN N L, REKAPALLY H, et al. N-cadherin gene expression in prostate carcinoma is modulated by integrin-dependent nuclear translocation of TWIST1[J]. Cancer Research, 2006, 66(7): 3365-3369. doi: 10.1158/0008-5472.CAN-05-3401
    [39]
    REN J, CROWLEY S D. TWIST1: a double-edged sword in kidney diseases[J]. Kidney Diseases, 2020, 6(4): 247-257. doi: 10.1159/000505188
    [40]
    YANG M H, HSU D S, WANG H W, et al. BMI1 is essential in TWIST1-induced epithelial-mesenchymal transition[J]. Nature Cell Biology, 2010, 12(10): 982-992. doi: 10.1038/ncb2099
    [41]
    XU Y, LEE D K, FENG Z, et al. Breast tumor cell-specific knockout of TWIST1 inhibits cancer cell plasticity, dissemination, and lung metastasis in mice[J]. Proceedings of the National Academy of Sciences, 2017, 114(43): 11494-11499. doi: 10.1073/pnas.1618091114
    [42]
    CASAS E, KIM J, BENDESKY A, et al. SNAIL2 is an essential mediator of TWIST1-induced epithelial mesenchymal transition and metastasis[J]. Cancer Research, 2011, 71(1): 245-254. doi: 10.1158/0008-5472.CAN-10-2330
    [43]
    TRAN D D, CORSA CAS, BISWAS H, et al. Temporal and spatial cooperation of SNAIL1 and TWIST1 during epithelial-mesenchymal transition predicts for human breast cancer recurrence[J]. Molecular Cancer Research, 2011, 9(12): 1644-1657. doi: 10.1158/1541-7786.MCR-11-0371
    [44]
    SUBBALAKSHMI A R, ASHRAF B, JOLLY M K. Biophysical and biochemical attributes of hybrid epithelial/mesenchymal phenotypes[J]. Physical Biology, 2022, 19(2): 025001. doi: 10.1088/1478-3975/ac482c
    [45]
    CUI J, ZHANG C, LEE J E, et al. MLL3 loss drives metastasis by promoting a hybrid epithelial-mesenchymal transition state[J]. Nature Cell Biology, 2023, 25(1): 145-158. doi: 10.1038/s41556-022-01045-0
    [46]
    MULLINS R D Z, PAL A, BARRETT T F, et al. Epithelial-mesenchymal plasticity in tumor immune evasion[J]. Cancer Research, 2022, 82(13): 2329-2343. doi: 10.1158/0008-5472.CAN-21-4370
    [47]
    ZHU H, MIAO R, WANG J, et al. Advances in modeling cellular mechanical perceptions and responses via the membrane-cytoskeleton-nucleus machinery[J]. Mechanobiology in Medicine, 2024, 2(1): 100040. doi: 10.1016/j.mbm.2024.100040
    [48]
    ZHANG C, ZHU H, REN X, et al. Mechanics-driven nuclear localization of YAP can be reversed by N-cadherin ligation in mesenchymal stem cells[J]. Nature Communications, 2021, 12(1): 6229. doi: 10.1038/s41467-021-26454-x
    [49]
    ZHANG Z, ZHU H, ZHAO G, et al. Programmable and reversible integrin-mediated cell adhesion reveals hysteresis in actin kinetics that alters subsequent mechanotransduction[J]. Advanced Science, 2023, 10(35): 2302421. doi: 10.1002/advs.202302421
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