Molecular mechanisms of epithelial-mesenchymal transition

被引:6452
|
作者
Lamouille, Samy [1 ,2 ]
Xu, Jian [3 ]
Derynck, Rik [1 ,2 ]
机构
[1] Univ Calif San Francisco, Ctr Regenerat Med & Stem Cell Res, Dept Cell & Tissue Biol & Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Regenerat Med & Stem Cell Res, Dept Eli & Edythe Broad, San Francisco, CA 94143 USA
[3] Univ So Calif, Ctr Craniofacial Mol Biol, Los Angeles, CA 90033 USA
基金
美国国家卫生研究院;
关键词
GROWTH-FACTOR-BETA; E-CADHERIN REPRESSION; CANCER-CELL INVASION; NF-KAPPA-B; TRANSCRIPTION FACTOR SNAIL; NEGATIVE FEEDBACK LOOP; REGULATES LUNG-CANCER; TGF-BETA; UP-REGULATION; GENE-EXPRESSION;
D O I
10.1038/nrm3758
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The transdifferentiation of epithelial cells into motile mesenchymal cells, a process known as epithelial-mesenchymal transition (EMT), is integral in development, wound healing and stem cell behaviour, and contributes pathologically to fibrosis and cancer progression. This switch in cell differentiation and behaviour is mediated by key transcription factors, including SNAIL, zinc-finger E-box-binding (ZEB) and basic helix-loop-helix transcription factors, the functions of which are finely regulated at the transcriptional, translational and post-translational levels. The reprogramming of gene expression during EMT, as well as non-transcriptional changes, are initiated and controlled by signalling pathways that respond to extracellular cues. Among these, transforming growth factor-beta (TGF beta) family signalling has a predominant role; however, the convergence of signalling pathways is essential for EMT.
引用
收藏
页码:178 / 196
页数:19
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