Phosphoinositide 3-OH kinase (PI3K) and PKB/Akt delay the onset of p53-mediated, transcriptionally dependent apoptosis

被引:122
|
作者
Sabbatini, P [1 ]
McCormick, F [1 ]
机构
[1] Univ Calif San Francisco, Sch Med, Inst Canc Res, San Francisco, CA 94143 USA
关键词
D O I
10.1074/jbc.274.34.24263
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 phosphoinositide 3-OH kinase (PI3K)-PKB/Akt signaling pathway has been shown to mediate both Ras- and cytokine-induced protection from apoptosis. In addition, apoptosis induced by the p53 tumor suppressor protein can be inhibited by Ras- and cytokine-mediated signaling pathways. It was therefore of interest to determine if the PI3K-PKB/Akt signaling pathway was capable of conferring protection from apoptosis induced by p53. We demonstrate in this report that constitutively active PI3K and PKB/Akt are capable of significantly delaying the onset of p53-mediated apoptosis. This was manifested as a delay in the kinetics of DNA degradation and cell death as well as a profound attenuation in the accumulation of cells with a sub-G, DNA content. Moreover, we found that this effect is mediated in the absence of changes in expression of Bcl-2, Bcl-XI, and the proapoptotic protein Pax. Our results provide the first direct and unambiguous link between p53-mediated apoptosis and the PI3K-PKB/Akt signaling pathway.
引用
收藏
页码:24263 / 24269
页数:7
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