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细胞周期蛋白D1抑制域介导前列腺癌的增殖和存活。

Cyclin D1 repressor domain mediates proliferation and survival in prostate cancer.

作者信息

Schiewer M J, Morey L M, Burd C J, Liu Y, Merry D E, Ho S-M, Knudsen K E

机构信息

Department of Cancer Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Oncogene. 2009 Feb 19;28(7):1016-27. doi: 10.1038/onc.2008.446. Epub 2008 Dec 15.

DOI:10.1038/onc.2008.446
PMID:19079343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2852245/
Abstract

Regulation of the androgen receptor (AR) is critical to prostate cancer (PCa) development; therefore, AR is the first line therapeutic target for disseminated tumors. Cell cycle-dependent accumulation of cyclin D1 negatively modulates the transcriptional regulation of AR through discrete, CDK4-independent mechanisms. The transcriptional corepressor function of cyclin D1 resides within a defined motif termed repressor domain (RD), and it was hypothesized that this motif could be utilized as a platform to develop new strategies for blocking AR function. Here, we demonstrate that expression of the RD peptide is sufficient to disrupt AR transcriptional activation of multiple, prostate-specific AR target genes. Importantly, these actions are sufficient to specifically inhibit S-phase progression in AR-positive PCa cells, but not in AR-negative cells or tested AR-positive cells of other lineages. As expected, impaired cell cycle progression resulted in a suppression of cell doubling. Additionally, cell death was observed in AR-positive cells that maintain androgen dependence and in a subset of castrate-resistant PCa cells, dependent on Akt activation status. Lastly, the ability of RD to cooperate with existing hormone therapies was examined, which revealed that RD enhanced the cellular response to an AR antagonist. Together, these data demonstrate that RD is sufficient to disrupt AR-dependent transcriptional and proliferative responses in PCa, and can enhance efficacy of AR antagonists, thus establishing the impetus for development of RD-based mimetics.

摘要

雄激素受体(AR)的调控对前列腺癌(PCa)的发展至关重要;因此,AR是播散性肿瘤的一线治疗靶点。细胞周期蛋白D1的细胞周期依赖性积累通过离散的、不依赖CDK4的机制对AR的转录调控产生负向调节作用。细胞周期蛋白D1的转录共抑制功能存在于一个称为抑制域(RD)的特定基序内,并且据推测该基序可作为开发阻断AR功能新策略的平台。在此,我们证明RD肽的表达足以破坏多个前列腺特异性AR靶基因的AR转录激活。重要的是,这些作用足以特异性抑制AR阳性PCa细胞中的S期进程,但对AR阴性细胞或其他谱系的经测试的AR阳性细胞则无此作用。正如预期的那样,细胞周期进程受损导致细胞倍增受到抑制。此外,在维持雄激素依赖性的AR阳性细胞以及一部分去势抵抗性PCa细胞中观察到细胞死亡,这取决于Akt激活状态。最后,研究了RD与现有激素疗法协同作用的能力,结果表明RD增强了细胞对AR拮抗剂的反应。总之,这些数据表明RD足以破坏PCa中AR依赖性的转录和增殖反应,并可增强AR拮抗剂的疗效,从而为基于RD的模拟物的开发提供了动力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/c73ade1d4736/nihms78288f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/c05cacedb5b6/nihms78288f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/c73ade1d4736/nihms78288f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/c05cacedb5b6/nihms78288f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/e432fe1bbb2c/nihms78288f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/bb689bc28b3a/nihms78288f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/7e57cddc85e2/nihms78288f4a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/2ec6a29d465d/nihms78288f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f8/2852245/c73ade1d4736/nihms78288f6.jpg

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