Sabbatini P, McCormick F
Cancer Research Institute, University of California, School of Medicine, San Francisco, California 94143-0128, USA.
J Biol Chem. 1999 Aug 20;274(34):24263-9. doi: 10.1074/jbc.274.34.24263.
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(1) DNA content. Moreover, we found that this effect is mediated in the absence of changes in expression of Bcl-2, Bcl-Xl, and the pro-apoptotic protein Bax. Our results provide the first direct and unambiguous link between p53-mediated apoptosis and the PI3K-PKB/Akt signaling pathway.
磷酸肌醇3 - 羟基激酶(PI3K)- PKB/Akt信号通路已被证明可介导Ras和细胞因子诱导的抗凋亡作用。此外,p53肿瘤抑制蛋白诱导的细胞凋亡可被Ras和细胞因子介导的信号通路抑制。因此,确定PI3K - PKB/Akt信号通路是否能够抵御p53诱导的细胞凋亡具有重要意义。我们在本报告中证明,组成型激活的PI3K和PKB/Akt能够显著延迟p53介导的细胞凋亡的发生。这表现为DNA降解和细胞死亡动力学的延迟,以及亚G1期DNA含量细胞积累的显著减少。此外,我们发现这种效应是在Bcl - 2、Bcl - Xl和促凋亡蛋白Bax表达没有变化的情况下介导的。我们的结果首次在p53介导的细胞凋亡与PI3K - PKB/Akt信号通路之间建立了直接且明确的联系。