Epidermal growth factor increased the expression of α2β1-integrin and modulated integrin-mediated signaling in human cervical adenocarcinoma cells

被引：24

作者：

Yamanaka, I ^{[1
]}

Koizumi, M ^{[1
]}

Baba, T ^{[1
]}

Yamashita, S ^{[1
]}

Suzuki, T ^{[1
]}

Kudo, R ^{[1
]}

机构：

[1] Sapporo Med Univ, Dept Obstet & Gynecol, Sch Med, Chuo Ku, Sapporo, Hokkaido 0600061, Japan

来源：

EXPERIMENTAL CELL RESEARCH | 2003年 / 286卷 / 02期

关键词：

cervical adenocarcinoma cells; EGF; alpha; 2; beta; 1-integrin; ZD1839; cell migration;

D O I：

10.1016/S0014-4827(03)00065-X

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Epidermal growth factor (EGF) receptor (EGFR) is involved in various basic biochemical pathways and is thus thought to play an important role in cell migration. We examined the effect of EGF on motility, migration, and morphology of a human adenocarcinoma cell line CAC-1. EGF treatment increased the motility of cervical adenocarcinoma cells and promoted migration of the cells on fibronectin and type IV collagen. EGF induced morphological changes with lamellipodia during EGFR-mediated motility. The results of an immunoprecipitation study showed that EGF up-regulated the expression of alpha2beta1-integrin in a dose-dependent manner. EGF-induced cell migration was blocked by alpha2beta1-integrin antibody. Our results also showed that EGF treatment stimulated the level of tyrosine dephosphorylation of FAK, which is required for EGF-induced changes in motility, migration, and cell morphology. A tyrosine kinase inhibitor (ZD1839) blocked EGF-induced changes in cervical adenocarcinoma cells. The results suggest that EGF promotes cell motility and migration and increases the expression of alpha2beta1-integrin, possibly by decreasing FAK phosphorylation. (C) 2003 Elsevier Science (USA). All rights reserved.

引用

页码：165 / 174

页数：10

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