The epithelial-mesenchymal transition under control: Global programs to regulate epithelial plasticity

被引:213
作者
Angela Nieto, M. [1 ]
Cano, Amparo [2 ]
机构
[1] UMH, CSIC, Inst Neurociencias, Alicante 03550, Spain
[2] UAM, CSIC, Inst Invest Biomed Alberto Sols, Dept Bioquim, Madrid 28029, Spain
关键词
EMT; Epithelial plasticity; Cancer; Sternness; Fibrosis; CANCER STEM-CELLS; GENE-EXPRESSION SIGNATURE; BREAST-CANCER; TRANSCRIPTION FACTORS; FIBROBLASTS DERIVE; LIVER FIBROSIS; FEEDBACK LOOP; E-CADHERIN; TUMOR; SNAIL;
D O I
10.1016/j.semcancer.2012.05.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The epithelial to mesenchymal transition or EMT has become one of the most exciting fields in cancer research. Nevertheless, its relevance in tumor biology and the metastatic process still faces some controversy. Clarification may arise when considering the EMT as a reversible and often incomplete process, essentially a manifestation of strong epithelial plasticity. Transient cellular states are generated to fulfill specific requirements in each and all the steps of the metastatic process, from primary tumor cell detachment to dissemination and colonization. Opposing multiple cellular programs that promote or prevent EMT, thereby destabilizing or reinforcing epithelial integrity, play a central role in the inherent cellular dynamics of cancer progression. These cell biology programs not only drive cells towards the epithelial or the mesenchymal state but also impinge into multiple cellular and global responses including proliferation, sternness, chemo and immunotherapy resistance, inflammation and immunity, all relevant for the development of the metastatic disease. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:361 / 368
页数:8
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