Signaling components involved in Bcl-w-induced migration of gastric cancer cells

被引:28
作者
Bae, In Hwa [1 ]
Yoon, Sung Hwan [1 ]
Lee, Seung Bum [1 ]
Park, Jong Kuk [1 ]
Ho, Jin-Nyoung [1 ]
Um, Hong-Duck [1 ]
机构
[1] Korea Inst Radiol & Med Sci, Lab Radiat Canc Biol, Seoul 139706, South Korea
关键词
Bcl-w; Migration; Cell signaling; Gastric carcinoma; FOCAL ADHESION KINASE; PLASMINOGEN-ACTIVATOR RECEPTOR; EXPRESSION; FAMILY; SUPPRESSES; PROTEINS; BLOCKING; CLONING; DEATH; ACID;
D O I
10.1016/j.canlet.2008.11.022
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
We have previously reported that Bcl-w enhances the invasiveness of gastric cancer cells by inducing MMP-2 expression via phosphoinositide 3-kinase (PI3K), Akt and Sp1. This study demonstrates that Bcl-w additionally induces uPA expression and FAK activation. Analyses of the hierarchical relationship and functions of these components showed that the PI3K-Akt-Sp1 pathway also mediates the induction of uPA, and that both uPA and MMP-2 contribute to Bcl-w-induced invasion via the stimulation of the FAK-dependent migratory pathway. These findings significantly advance our understandings of the Bcl-w-induced signaling processes that results in the migration and invasion of cancer cells. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:22 / 28
页数:7
相关论文
共 23 条
[1]
The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]
Bax and other pro-apoptotic Bcl-2 family "killer-proteins" and their victim, the mitochondrion [J].
Antonsson, B .
CELL AND TISSUE RESEARCH, 2001, 306 (03) :347-361
[3]
Bcl-w promotes gastric cancer cell invasion by inducing matrix metalloproteinase-2 expression via phosphoinositide 3-kinase, Akt, and Sp1 [J].
Bae, In Hwa ;
Park, Myung-Jin ;
Yoon, Sung Hwan ;
Kang, Sung Wook ;
Lee, Seung-Sook ;
Choi, Kyung-Mi ;
Um, Hong-Duck .
CANCER RESEARCH, 2006, 66 (10) :4991-4995
[4]
Plasminogen activation and cancer [J].
Dano, K ;
Behrendt, N ;
Hoyer-Hansen, G ;
Johnsen, M ;
Lund, LR ;
Ploug, M ;
Romer, J .
THROMBOSIS AND HAEMOSTASIS, 2005, 93 (04) :676-681
[5]
Inhibition of focal adhesion kinase (FAK) signaling in focal adhesions decreases cell motility and proliferation [J].
Gilmore, AP ;
Romer, LH .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (08) :1209-1224
[6]
BCL-2 family members and the mitochondria in apoptosis [J].
Gross, A ;
McDonnell, JM ;
Korsmeyer, SJ .
GENES & DEVELOPMENT, 1999, 13 (15) :1899-1911
[7]
Gene expression profile of glioblastoma multiforme invasive phenotype points to new therapeutic targets [J].
Hoelzinger, DB ;
Mariani, L ;
Weis, J ;
Woyke, T ;
Berens, TJ ;
McDonough, WS ;
Sloan, A ;
Coons, SW ;
Berens, ME .
NEOPLASIA, 2005, 7 (01) :7-16
[8]
c-Myc is essential for urokinase plasminogen activator expression on hypoxia-induced vascular smooth muscle cells [J].
Hou, YongZhong ;
Okamoto, Chikako ;
Okada, Kiyotaka ;
Kawao, Naoyaki ;
Kawata, Shuhei ;
Ueshima, Shigeru ;
Matsuo, Osamu .
CARDIOVASCULAR RESEARCH, 2007, 75 (01) :186-194
[9]
Kim DK, 2001, J CELL SCI, V114, P4329
[10]
BOVINE UROKINASE-TYPE PLASMINOGEN-ACTIVATOR AND ITS RECEPTOR - CLONING AND INDUCTION BY RETINOIC ACID [J].
KRATZSCHMAR, J ;
HAENDLER, B ;
KOJIMA, S ;
RIFKIN, DB ;
SCHLEUNING, WD .
GENE, 1993, 125 (02) :177-183