Cadherins and cancer: how does cadherin dysfunction promote tumor progression?

被引:634
作者
Jeanes, A. [1 ]
Gottardi, C. J. [2 ]
Yap, A. S. [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Mol Cell Biol Div, Brisbane, Qld, Australia
[2] Northwestern Univ, Dept Med, Feinberg Sch Med, Chicago, IL 60611 USA
基金
英国医学研究理事会;
关键词
E-cadherin; beta-catenin; Wnt; growth factor receptor; cell polarity; metastasis;
D O I
10.1038/onc.2008.343
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has long been recognized that the cell-cell adhesion receptor, E-cadherin, is an important determinant of tumor progression, serving as a suppressor of invasion and metastasis in many contexts. Yet how the loss of E-cadherin function promotes tumor progression is poorly understood. In this review, we focus on three potential underlying mechanisms: the capacity of E-cadherin to regulate beta-catenin signaling in the canonical Wnt pathway; its potential to inhibit mitogenic signaling through growth factor receptors and the possible links between cadherins and the molecular determinants of epithelial polarity. Each of these potential mechanisms provides insights into the complexity that is likely responsible for the tumor-suppressive action of E-cadherin.
引用
收藏
页码:6920 / 6929
页数:10
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