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
相关论文
共 33 条
[1]   Regulated binding of a PTP1B-like phosphatase to N-cadherin: Control of cadherin-mediated adhesion by dephosphorylation of beta-catenin [J].
Balsamo, J ;
Leung, TC ;
Ernst, H ;
Zanin, MKB ;
Hoffman, S ;
Lilien, J .
JOURNAL OF CELL BIOLOGY, 1996, 134 (03) :801-813
[2]  
BECKER KF, 1994, CANCER RES, V54, P3845
[3]  
BERGER MS, 1988, CANCER RES, V48, P1238
[4]  
BIRCHMEIER W, 1993, J CELL SCI, P159
[5]   INSULIN-LIKE GROWTH FACTOR-I ACTIVATES THE INVASION SUPPRESSOR FUNCTION OF E-CADHERIN IN MCF-7 HUMAN MAMMARY-CARCINOMA CELLS IN-VITRO [J].
BRACKE, ME ;
VYNCKE, BM ;
BRUYNEEL, EA ;
VERMEULEN, SJ ;
DEBRUYNE, GK ;
VANLAREBEKE, NA ;
VLEMINCKX, K ;
VANROY, FM ;
MAREEL, MM .
BRITISH JOURNAL OF CANCER, 1993, 68 (02) :282-289
[6]   RECEPTOR PROTEIN-TYROSINE-PHOSPHATASE PTP-MU ASSOCIATES WITH CADHERINS AND CATENINS IN-VIVO [J].
BRADYKALNAY, SM ;
RIMM, DL ;
TONKS, NK .
JOURNAL OF CELL BIOLOGY, 1995, 130 (04) :977-986
[7]  
BRINGUIER PP, 1993, CANCER RES, V53, P3241
[8]   TARGETING OF THE SF HGF RECEPTOR TO THE BASOLATERAL DOMAIN OF POLARIZED EPITHELIAL-CELLS [J].
CREPALDI, T ;
POLLACK, AL ;
PRAT, M ;
ZBOREK, A ;
MOSTOV, K ;
COMOGLIO, PM .
JOURNAL OF CELL BIOLOGY, 1994, 125 (02) :313-320
[9]   OVEREXPRESSION OF ERBB2 IN HUMAN MAMMARY EPITHELIAL-CELLS SIGNALS INHIBITION OF TRANSCRIPTION OF THE E-CADHERIN GENE [J].
DSOUZA, B ;
TAYLORPAPADIMITRIOU, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :7202-7206
[10]   BETA-CATENIN MEDIATES THE INTERACTION OF THE CADHERIN CATENIN COMPLEX WITH EPIDERMAL GROWTH-FACTOR RECEPTOR [J].
HOSCHUETZKY, H ;
ABERLE, H ;
KEMLER, R .
JOURNAL OF CELL BIOLOGY, 1994, 127 (05) :1375-1380