Regulation of tumor angiogenesis by integrin-linked kinase (ILK)

被引:258
|
作者
Tan, C
Cruet-Hennequart, S
Troussard, A
Fazli, L
Costello, P
Sutton, K
Wheeler, J
Gleave, M
Sanghera, J
Dedhar, S
机构
[1] Vancouver Hosp, Prostate Ctr, BC Canc Agcy, Vancouver, BC V6H 3Z6, Canada
[2] Univ British Columbia, Jack Bell Res Ctr, Dept Biochem & Mol Biol, Vancouver, BC V6H 3Z6, Canada
[3] Kinetek Pharmaceut Inc, Vancouver, BC V6P 5G6, Canada
关键词
D O I
10.1016/S1535-6108(03)00281-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We show that integrin-linked kinase (ILK) stimulates the expression of VEGF by stimulating HIF-1alpha protein expression in a PKB/Akt- and mTOR/FRAP-dependent manner. In human Prostate cancer cells, knockdown of ILK expression with siRNA, or inhibition of ILK activity, results in significant inhibition of HIF-1alpha and VEGF expression. In endothelial cells, VEGF stimulates ILK activity, and inhibition of ILK expression or activity results in the inhibition of VEGF-mediated endothelial cell migration, capillary formation in vitro, and angiogenesis in vivo. Inhibition of ILK activity also inhibits prostate tumor angiogenesis and suppresses tumor growth. These data demonstrate an important and essential role of ILK in two key aspects of tumor angiogenesis: VEGF expression by tumor cells and VEGF-stimulated blood vessel formation.
引用
收藏
页码:79 / 90
页数:12
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