Mdm2 and HIF-1α interaction in tumor cells during hypoxia

被引:74
|
作者
Nieminen, AL
Qanungo, S
Schneider, EA
Jiang, BH
Agani, FH
机构
[1] Case Western Reserve Univ, Sch Med, Case Comprehens Canc Ctr Labs, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Anat, Cleveland, OH 44106 USA
[3] W Virginia Univ, Mary Babb Randolph Canc Ctr, Dept Microbiol Immunol & Cell Biol, Morgantown, WV 26506 USA
关键词
D O I
10.1002/jcp.20406
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The interaction between HIF-1 alpha, Mdm2, and p53 proteins during hypoxia has received recent attention. Here, we investigated the consequences of interaction between HIF-1 alpha and Mdm2 under hypoxic conditions. Endogenous HIF-1 alpha and Mdm2 proteins were co-immunoprecipitated from lysates of hypoxic HCT116 p53WT and p53(-/-) cells, suggesting that association of these two proteins is a p53-independent event. The cellular Mdm2 protein content was not significantly altered in hypoxic tumor cells. Overexpression of Mdm2 resulted in an increase in HIF-1 alpha protein content in hypoxic cells and increased hypoxia-induced vascular endothelial growth factor (VEGF) transcriptional activation. These results point toward a novel and p53-independent function of Mdm2 to promote tumor cell adaptations to hypoxia by interacting with and promoting HIF-1 activation. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:364 / 369
页数:6
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