ZBTB7A Mediates the Transcriptional Repression Activity of the Androgen Receptor in Prostate Cancer

被引:22
作者
Han, Dong [1 ]
Chen, Sujun [2 ,3 ]
Han, Wanting [1 ]
Gao, Shuai [1 ]
Owiredu, Jude N. [1 ]
Li, Muqing [1 ]
Balk, Steven P. [4 ]
He, Housheng Hansen [2 ,3 ]
Cai, Changmeng [1 ]
机构
[1] Univ Massachusetts, Ctr Personalized Canc Therapy, Boston, MA 02125 USA
[2] Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON M5G 1L7, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[4] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
基金
加拿大自然科学与工程研究理事会;
关键词
LONG NONCODING RNA; TUMOR-SUPPRESSOR; EXPRESSION; RESISTANCE; PROLIFERATION; RECRUITMENT; MECHANISMS; TARGET; PCAT-1;
D O I
10.1158/0008-5472.CAN-19-0815
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Loss of expression of context-specific tumor suppressors is a critical event that facilitates the development of prostate cancer. Zinc finger and BTB domain containing transcriptional repressors, such as ZBTB7A and ZBTB16, have been recently identified as tumor suppressors that play important roles in preventing prostate cancer progression. In this study, we used combined ChIP-seq and RNA-seq analyses of prostate cancer cells to identify direct ZBTB7A-repressed genes, which are enriched for transcriptional targets of E2F, and identified that the androgen receptor (AR) played a critical role in the transcriptional suppression of these E2F targets. AR recruitment of the retinoblastoma protein (Rb) was required to strengthen the E2F-Rb transcriptional repression complex. In addition, ZBTB7A was rapidly recruited to the E2F-Rb binding sites by AR and negatively regulated the transcriptional activity of E2F1 on DNA replication genes. Finally, ZBTB7A suppressed the growth of castration-resistant prostate cancer (CRPC) in vitro and in vivo, and overexpression of ZBTB7A acted in synergy with high-dose testosterone treatment to effectively prevent the recurrence of CRPC. Overall, this study provides novel molecular insights of the role of ZBTB7A in CRPC cells and demonstrates globally its critical role in mediating the transcriptional repression activity of AR. Significance: ZBTB7A is recruited to the E2F-Rb binding sites by AR and negatively regulates the transcriptional activity of E2F1 on DNA replication genes.
引用
收藏
页码:5260 / 5271
页数:12
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