Cooperation, amplification, and feed-back in epithelial-mesenchymal transition

被引:49
作者
Garcia de Herreros, Antonio [1 ]
Baulida, Josep [1 ]
机构
[1] Hosp Mar, IMIM, Barcelona 08003, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2012年 / 1825卷 / 02期
关键词
EMT; Snail1; E-cadherin; NF-KAPPA-B; TRANSCRIPTION FACTOR SNAIL; REPRESSES E-CADHERIN; VITAMIN-D-RECEPTOR; BETA-CATENIN; MASTER REGULATOR; GENE-EXPRESSION; MIR-200; FAMILY; UP-REGULATION; PROTEIN;
D O I
10.1016/j.bbcan.2012.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The epithelial to mesenchymal transition (EMT) consists of a rapid change of cell phenotype, characterized by the loss of epithelial traits and the acquisition of a more motile phenotype reminiscent of a fibroblast. The study of this process has received considerable attention because of its potential role in the acquisition of several cancer traits, particularly in cell invasion. In this article we describe the current knowledge of the molecular mechanisms governing this transition. In particular we discuss how initiation of EMT is dependent on the mutually exclusive levels of the transmembrane cell to cell adhesion molecule E-cadherin and its transcriptional repressor Snail1 and how Snail1 and other E-cadherin transcriptional repressors drive the EMT process. We focus on several new aspects of Snail1 regulation and propose a model for understanding the initiation and progression of this transition, based on the existence of feed-back mechanisms that limit or amplify the response to extracellular cues. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:223 / 228
页数:6
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