Department of Medicinal Chemistry and Molecular Pharmacology and the Purdue University Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.
Mol Cell Endocrinol. 2013 Jun 15;372(1-2):12-22. doi: 10.1016/j.mce.2013.03.004. Epub 2013 Mar 21.
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.
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。