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c-Jun 的转录活性对于抑制 AR 功能至关重要。

Transcriptional activity of c-Jun is critical for the suppression of AR function.

机构信息

Department of Medicinal Chemistry and Molecular Pharmacology and the Purdue University Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.

出版信息

Mol Cell Endocrinol. 2013 Jun 15;372(1-2):12-22. doi: 10.1016/j.mce.2013.03.004. Epub 2013 Mar 21.

Abstract

Androgen receptor (AR) signaling plays a pivotal role in growth and survival of prostate cancer cells. c-Jun is an important member of the activator protein 1 (AP-1) family and was shown to interact with AR. However, the role of c-Jun in AR signaling remains controversial, with being a coactivator or a corepressor reported. Here, utilizing multiple approaches, we show that c-Jun efficiently inhibits AR activity and the growth of prostate cancer cells. Overexpression of c-Jun inhibits not only the activities of various androgen-responsive promoters but also the transcripts of multiple AR target genes. Interestingly, long-term c-Jun overexpression also down-regulates AR expression at both the protein and mRNA levels. Molecular analysis suggests that c-Jun inhibits AR transactivation potential via an unknown target gene. The inhibition of AR by c-Jun occurs in both hormone naïve and castration-resistant prostate cancer cells. Our results unravel a novel mechanism by which c-Jun antagonizes the AR signaling.

摘要

雄激素受体(AR)信号在前列腺癌细胞的生长和存活中起着关键作用。c-Jun 是激活蛋白 1(AP-1)家族的重要成员,已被证明与 AR 相互作用。然而,c-Jun 在 AR 信号中的作用仍存在争议,有报道称其既是共激活剂又是核心抑制剂。在这里,我们利用多种方法表明 c-Jun 能有效地抑制 AR 活性和前列腺癌细胞的生长。c-Jun 的过表达不仅抑制了各种雄激素反应启动子的活性,还抑制了多个 AR 靶基因的转录本。有趣的是,长期过表达 c-Jun 也会下调 AR 在蛋白质和 mRNA 水平的表达。分子分析表明,c-Jun 通过未知的靶基因抑制 AR 的转录激活潜能。c-Jun 对 AR 的抑制作用发生在激素敏感和去势抵抗的前列腺癌细胞中。我们的研究结果揭示了 c-Jun 拮抗 AR 信号的新机制。

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