Akt suppresses androgen-induced apoptosis by phosphorylating and inhibiting androgen receptor

被引:334
作者
Lin, HK
Yeh, SY
Kang, HY
Chang, CS
机构
[1] Univ Rochester, George Whipple Lab Canc Res, Dept Pathol, Rochester, NY 14642 USA
[2] Univ Rochester, Dept Urol, Rochester, NY 14642 USA
[3] Univ Rochester, Dept Radiat Oncol, Rochester, NY 14642 USA
[4] Univ Rochester, Ctr Canc, Rochester, NY 14642 USA
关键词
D O I
10.1073/pnas.121173298
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Whereas several apoptosis-related proteins have been linked to the antiapoptotic effects of Akt serine-threonine kinase, the search continues to explain the Akt signaling role in promoting cell survival via antiapoptotic effects. Here, we demonstrate that Akt phosphorylates the androgen receptor (AR) at Ser-210 and Ser-790, A mutation at AR Ser-210 results in the reversal of Akt-mediated suppression of AR transactivation. Activation of the phosphatidyl-inositol-3-OH kinase/Akt pathway results in the suppression of AR target genes, such as p21, and the decrease of androgen/AR-mediated apoptosis, which may involve the inhibition of interaction between AR and AR coregulators, Together, these findings provide a molecular basis for cross-talk between two signaling pathways at the level of Akt and AR-AR coregulators that may help us to better understand the roles of Akt in the androgen/AR-mediated apoptosis.
引用
收藏
页码:7200 / 7205
页数:6
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