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Targeting castration-resistant prostate cancer with a novel ROR

机译:用新颖的ROR定位抵抗抗阉割前列腺癌

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摘要

Prostate cancer (PCa) patients who progress to metastatic castration-resistant PCa (mCRPC) mostly have poor outcomes due to the lack of effective therapies. Our recent study established the orphan nuclear receptor RORγ as a novel therapeutic target for CRPC. Here, we reveal that elaiophylin (Elai), an antibiotic from Actinomycete streptomyces, is a novel RORγ antagonist and showed potent antitumor activity against CRPC in vitro and in vivo. We demonstrated that Elai selectively binded to RORγ protein and potently blocked RORγ transcriptional regulation activities. Structure–activity relationship studies showed that Elai occupied the binding pocket with several key interactions. Furthermore, Elai markedly reduced the recruitment of RORγ to its genomic DNA response element (RORE), suppressed the expression of RORγ target genes AR and AR variants, and significantly inhibited PCa cell growth. Importantly, Elai strongly suppressed tumor growth in both cell line based and patient-derived PCa xenograft models. Taken together, these results suggest that Elai is novel therapeutic RORγ inhibitor that can be used as a drug candidate for the treatment of human CRPC.
机译:前列腺癌(PCA)转移阉割抵抗力PCA(MCRPC)的患者主要具有较差的结果,由于缺乏有效的疗法。我们最近的研究将孤儿核受体RORγ作为CRPC的新疗法靶向。在这里,我们揭示了Elaiophylin(Elai),来自辐射瘤素链霉菌的抗生素是一种新的Rorγ拮抗剂,并在体外和体内显示出对CRPC的有效抗肿瘤活性。我们证明Elai选择性地结合RORγ蛋白,并且有效地阻断了RORγ转录调节活动。结构 - 活性关系研究表明,Elai占用了具有几个关键相互作用的装订口袋。此外,Elai显着降低了RORγ的募集到其基因组DNA响应元件(RORE),抑制了RORγ靶基因AR和AR变体的表达,并显着抑制了PCA细胞生长。重要的是,Elai在基于细胞系和患者衍生的PCA异种移植模型中强制抑制肿瘤生长。总之,这些结果表明Elai是新的治疗性RORγ抑制剂,可用作治疗人类CRPC的药物候选物。

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