Howard Hughes Medical Institute, Department of Medicine, University of California San Diego, La Jolla 92093, USA.
Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Nature. 2013 Aug 29;500(7464):598-602. doi: 10.1038/nature12451. Epub 2013 Aug 14.
Although recent studies have indicated roles of long non-coding RNAs (lncRNAs) in physiological aspects of cell-type determination and tissue homeostasis, their potential involvement in regulated gene transcription programs remains rather poorly understood. The androgen receptor regulates a large repertoire of genes central to the identity and behaviour of prostate cancer cells, and functions in a ligand-independent fashion in many prostate cancers when they become hormone refractory after initial androgen deprivation therapy. Here we report that two lncRNAs highly overexpressed in aggressive prostate cancer, PRNCR1 (also known as PCAT8) and PCGEM1, bind successively to the androgen receptor and strongly enhance both ligand-dependent and ligand-independent androgen-receptor-mediated gene activation programs and proliferation in prostate cancer cells. Binding of PRNCR1 to the carboxy-terminally acetylated androgen receptor on enhancers and its association with DOT1L appear to be required for recruitment of the second lncRNA, PCGEM1, to the androgen receptor amino terminus that is methylated by DOT1L. Unexpectedly, recognition of specific protein marks by PCGEM1-recruited pygopus 2 PHD domain enhances selective looping of androgen-receptor-bound enhancers to target gene promoters in these cells. In 'resistant' prostate cancer cells, these overexpressed lncRNAs can interact with, and are required for, the robust activation of both truncated and full-length androgen receptor, causing ligand-independent activation of the androgen receptor transcriptional program and cell proliferation. Conditionally expressed short hairpin RNA targeting these lncRNAs in castration-resistant prostate cancer cell lines strongly suppressed tumour xenograft growth in vivo. Together, these results indicate that these overexpressed lncRNAs can potentially serve as a required component of castration-resistance in prostatic tumours.
虽然最近的研究表明长非编码 RNA(lncRNA)在细胞类型决定和组织稳态的生理方面发挥作用,但它们在调节基因转录程序中的潜在作用仍知之甚少。雄激素受体调节着与前列腺癌细胞特征和行为相关的大量基因,在许多前列腺癌中,当它们在初始雄激素剥夺治疗后变得对激素不敏感时,以非配体依赖的方式发挥作用。在这里,我们报告两种在侵袭性前列腺癌中高度过表达的 lncRNA,PRNCR1(也称为 PCAT8)和 PCGEM1,先后与雄激素受体结合,并强烈增强配体依赖性和配体非依赖性雄激素受体介导的基因激活程序以及前列腺癌细胞的增殖。PRNCR1 与增强子上羧基末端乙酰化的雄激素受体结合及其与 DOT1L 的关联似乎是第二个 lncRNA PCGEM1 募集到雄激素受体氨基末端所必需的,该末端被 DOT1L 甲基化。出乎意料的是,PCGEM1 募集的 pygopus 2 PHD 结构域识别特定的蛋白质标记,增强了这些细胞中雄激素受体结合增强子的特异性环化,以靶向基因启动子。在“耐药”前列腺癌细胞中,这些过表达的 lncRNA 可以与截断和全长雄激素受体相互作用,并且是其强烈激活所必需的,导致雄激素受体转录程序和细胞增殖的非配体依赖性激活。在去势抵抗性前列腺癌细胞系中,针对这些 lncRNA 的条件表达短发夹 RNA 强烈抑制了体内肿瘤异种移植物的生长。总之,这些结果表明这些过表达的 lncRNA 可能成为前列腺肿瘤去势抵抗的必需组成部分。