P70S6K 1 regulation of angiogenesis through VEGF and HIF-1α expression

被引:71
|
作者
Bian, Chuan-Xiu [2 ]
Shi, Zhumei [2 ]
Meng, Qiao [1 ]
Jiang, Yue [1 ]
Liu, Ling-Zhi [1 ]
Jiang, Bing-Hua [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[2] Nanjing Med Univ, Ctr Canc, Dept Pathol, Nanjing 210029, Peoples R China
基金
中国国家自然科学基金;
关键词
p70S6K1; VEGF; HIF-1; Tumor angiogenesis; siRNA; ENDOTHELIAL GROWTH-FACTOR; PHOSPHATIDYLINOSITOL; 3-KINASE; MAMMALIAN TARGET; OVARIAN-CANCER; SIGNALING PATHWAY; KINASE-ACTIVITY; MTOR; RAPAMYCIN; CELLS; TRANSLATION;
D O I
10.1016/j.bbrc.2010.06.080
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
The 70 kDa ribosomal S6 kinase 1 (p70S6K1), a downstream target of phosphoinositide 3-kinase (PI3K) and ERK mitogen-activated protein kinase (MAPK), is an important regulator of cell cycle progression, and cell proliferation. Recent studies indicated an important role of p70S6K1 in PTEN-negative and AKT-overexpressing tumors. However, the mechanism of p70S6K1 in tumor angiogenesis remains to be elucidated. In this study, we specifically inhibited p70S6K1 activity in ovarian cancer cells using vector-based small interfering RNA (siRNA) against p70S6K1. We found that knockdown of p70S6K1 significantly decreased VEGF protein expression and VEGF transcriptional activation through the HIF-1 alpha binding site at its enhancer region. The expression of p70S6K1 siRNA specifically inhibited but HIF-1 alpha, but not HIF-1 beta protein expression. We also found that p70S6K1 down-regulation inhibited ovarian tumor growth and angiogenesis, and decreased cell proliferation and levels of VEGF and HIF-1 alpha expression in tumor tissues. Our results suggest that p70S6K1 is required for tumor growth and angiogenesis through HIF-1 alpha and VEGF expression, providing a molecular mechanism of human ovarian cancer mediated by p70S6K1 signaling. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:395 / 399
页数:5
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