MicroRNA let-7c Suppresses Androgen Receptor Expression and Activity via Regulation of Myc Expression in Prostate Cancer Cells

被引:160
作者
Nadiminty, Nagalakshmi [1 ]
Tummala, Ramakumar
Lou, Wei
Zhu, Yezi
Zhang, Jin [3 ]
Chen, Xinbin [2 ]
White, Ralph W. deVere [2 ]
Kung, Hsing-Jien [2 ,4 ]
Evans, Christopher P. [2 ]
Gao, Allen C. [1 ,2 ]
机构
[1] Univ Calif Davis, Med Ctr, Dept Urol, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Ctr Canc, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Comparat Oncol Lab, Sch Vet Med, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
基金
美国国家卫生研究院;
关键词
STAT3; ACTIVATION; PROGRESSION; LIN28; NF-KAPPA-B2/P52; DIFFERENTIATION; ANTIANDROGEN; ONCOGENE; PROFILES; THERAPY; MIRNAS;
D O I
10.1074/jbc.M111.278705
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
Castration-resistant prostate cancer continues to rely on androgen receptor (AR) expression. AR plays a central role in the development of prostate cancer and progression to castration resistance during and after androgen deprivation therapy. Here, we identified miR-let-7c as a key regulator of expression of AR. miR-let-7c suppresses AR expression and activity in human prostate cancer cells by targeting its transcription via c-Myc. Suppression of AR by let-7c leads to decreased cell proliferation of human prostate cancer cells. Down-regulation of Let-7c in prostate cancer specimens is inversely correlated with AR expression, whereas the expression of Lin28 (a repressor of let-7) is correlated positively with AR expression. Our study demonstrates that the miRNA let-7c plays an important role in the regulation of androgen signaling in prostate cancer by down-regulating AR expression. These results suggest that reconstitution of miR-let-7c may aid in targeting enhanced and hypersensitive AR in advanced prostate cancer.
引用
收藏
页码:1527 / 1537
页数:11
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