Increase of androgen-induced cell death and androgen receptor transactivation by BRCA1 in prostate cancer cells

被引:126
作者
Yeh, SY
Hu, YC
Rahman, M
Lin, HK
Hsu, CL
Ting, HJ
Kang, HY
Chang, CS
机构
[1] Univ Rochester, George Whipple Lab Canc Res, Dept Urol, Rochester, NY 14642 USA
[2] Univ Rochester, Dept Pathol, Rochester, NY 14642 USA
[3] Univ Rochester, Dept Radiat Oncol, Rochester, NY 14642 USA
[4] Univ Rochester, Dept Biochem, Rochester, NY 14642 USA
[5] Univ Rochester, Dept Toxicol, Rochester, NY 14642 USA
[6] Univ Rochester, Ctr Canc, Rochester, NY 14642 USA
关键词
D O I
10.1073/pnas.190353897
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
Although mutations of the breast cancer susceptibility gene 1 (BRCA1) may play important roles in breast and prostate cancers, the detailed mechanism linking the functions of BRCA1 to these two hormone-related tumors remains to be elucidated. Here, we report that BRCA1 interacts with androgen receptor (AR) and enhances AR target genes, such as p21((WAF1/CIP1)), that may result in the increase of androgen-induced cell death in prostate cancer cells. The BRCA1-enhanced AR transactivation can be further induced synergistically with AR coregulators. such as CBP, ARA55, and ARA70, Together, these data suggest that the BRCA1 may function as an AR coregulator and play positive roles in androgen-induced cell death in prostate cancer cells and other androgen/AR target organs.
引用
收藏
页码:11256 / 11261
页数:6
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