The E-cadherin/epidermal growth factor receptor interaction: A hypothesis of reciprocal and reversible control of intercellular adhesion and cell proliferation

被引:0
作者
Jawhari, AU
Farthing, MJG
Pignatelli, M
机构
[1] Hammersmith Hosp, Imperial Coll, Sch Med, Div Diagnost & Investigat Sci, London W12 0NN, England
[2] St Bartholomews & Royal London Sch Med & Dent, Digest Dis Res Ctr, London E1 2AT, England
关键词
E-cadherin; epidermal growth factor receptor; EGFR; cell adhesion molecule;
D O I
10.1002/(SICI)1096-9896(199901)187:2<155::AID-PATH193>3.0.CO;2-E
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The E-cadherin/catenin complex is a calcium-dependent cell-cell adhesion molecule, whose function is critical to the integrity of the adherens junction and which plays a role in the establishment and maintenance of normal epithelial morphology and differentiation. Loss of E-cadherin-mediated adhesion appears to be a fundamental aspect of the neoplastic phenotype which in some cases appears to be mediated by post-translational modifications (i.e. tyrosine phosphorylation) of its interacting proteins, the catenins which link E-cadherin to the actin cytoskeleton. There is increasing experimental evidence to suggest that epidermal growth factor receptor tyrosine phosphorylation may lead to the inactivation of the E-cadherin/catenin complex in cancer cells through its interaction with beta- or gamma-catenin in the cytoskeleton. Modulation of epidermal growth factor receptor activity by pharmacological agents has the potential to regulate a variety of cellular processes including adhesion, differentiation, and proliferation. Copyright (C) 1999 John Wiley & Sons, Ltd.
引用
收藏
页码:155 / 157
页数:3
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