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G-四链体配体下调雄激素受体使去势抵抗性前列腺癌细胞对恩杂鲁胺敏感。

Down-Regulation of the Androgen Receptor by G-Quadruplex Ligands Sensitizes Castration-Resistant Prostate Cancer Cells to Enzalutamide.

机构信息

Department of Molecular Medicine , University of Padua , via A. Gabelli 63 , 35121 Padua , Italy.

Department of Applied Research and Technological Development , Fondazione IRCCS Istituto Nazionale dei Tumori di Milano , Via G. A. Amadeo 42 , 20133 Milan , Italy.

出版信息

J Med Chem. 2018 Oct 11;61(19):8625-8638. doi: 10.1021/acs.jmedchem.8b00502. Epub 2018 Sep 20.

Abstract

Stabilization of the G-quadruplexes (G4s) within the androgen receptor (AR) gene promoter to block transcription may represent an innovative approach to interfere with aberrant AR signaling in castration resistant prostate cancer (CRPC). A library of differently functionalized naphthalene diimides (NDIs) was screened for their ability to stabilize AR G4s: the core-extended NDI (7) stood out as the most promising ligand. AR-positive cells were remarkably sensitive to 7 in comparison to AR-negative CRCP or normal prostate epithelial cells; 7 induced remarkable impairment of AR mRNA and protein amounts and significant perturbations in the expression levels of KLK3 and of genes involved in the activation of AR program via feedback mechanisms. Moreover, 7 synergistically interacted with Enzalutamide, an inhibitor of AR signaling used in second-line therapies. Overall, our data show that stabilization of AR G4s may represent an alternative treatment options for CRPC and other malignancies relying on aberrant androgen signaling.

摘要

稳定雄激素受体 (AR) 基因启动子中的 G-四链体 (G4s) 以阻止转录可能代表一种创新的方法来干扰去势抵抗性前列腺癌 (CRPC) 中异常的 AR 信号。筛选了一系列不同功能化的萘二酰亚胺 (NDIs),以研究它们稳定 AR G4s 的能力:核心扩展的 NDI (7) 脱颖而出,成为最有前途的配体。与 AR 阴性的 CRPC 或正常前列腺上皮细胞相比,AR 阳性细胞对 7 非常敏感;7 诱导 AR mRNA 和蛋白数量的显著减少,并通过反馈机制显著扰乱 KLK3 和参与 AR 程序激活的基因的表达水平。此外,7 与恩杂鲁胺(一种用于二线治疗的 AR 信号抑制剂)协同作用。总的来说,我们的数据表明,稳定 AR G4s 可能代表治疗 CRPC 和其他依赖异常雄激素信号的恶性肿瘤的另一种治疗选择。

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