CD44 signaling through focal adhesion kinase and its anti-apoptotic effect

被引:93
作者
Fujita, Y
Kitagawa, M
Nakamura, S
Azuma, K
Ishii, G
Higashi, M
Kishi, H
Hiwasa, T
Koda, K
Nakajima, N
Harigaya, K
机构
[1] Chiba Univ, Grad Sch Med, Dept Mol & Tumor Pathol, Chuo Ku, Chiba 2608670, Japan
[2] Chiba Univ, Grad Sch Med, Dept Gen Surg, Chuo Ku, Chiba 2608670, Japan
[3] Chiba Univ, Grad Sch Med, Dept Biochem & Genet, Chuo Ku, Chiba 2608670, Japan
关键词
CD44; signal transduction; focal adhesion kinase; phosphatidylinositol; 3-kinase; mitogen-activated protein kinase; apoptosis;
D O I
10.1016/S0014-5793(02)03262-3
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
Adhesion molecules can initiate intracellular signaling. Engagement of CD44 either by its natural ligand hyaluronan or a specific antibody on a cell line induced tyrosine phosphorylation and activation of focal adhesion kinase (FAK), which then associated with phosphatidylinositol 3-kinase (PI3K) and activated mitogen-activated protein kinase at its downstream. However, the introduction of dominant negative Rho into the cells inhibited the CD44-stimulated FAK phosphorylation. Cells expressing CD44 were significantly resistant to etoposide-induced apoptosis. This anti-apoptotic effect was cancelled by the inhibition of either Rho, FAK or PI3K. These results may indicate a signaling pathway from CD44 to mediate the resistance against drug-induced apoptosis in cancer cells. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:101 / 108
页数:8
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