治疗前列腺癌的雄激素受体抑制剂。

Ryan N Cole, Qinghua Fang, Kanako Matsuoka, Zhou Wang
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引用次数: 0

摘要

摘要:雄激素在前列腺癌的发生和发展过程中起着重要作用。雄激素的作用是通过雄激素受体(AR)介导的,AR是一种依赖配体的DNA结合转录因子。可以说,AR 是治疗前列腺癌最重要的靶点。目前美国食品和药物管理局(FDA)批准的AR抑制剂以配体结合域(LBD)为靶点,对前列腺癌患者具有疗效,尤其是与雄激素剥夺疗法联合使用时。遗憾的是,接受目前已获批准的 AR 靶向药物治疗的患者会产生耐药性,并复发阉割抗性前列腺癌(CRPC)。导致 CRPC 的主要机制涉及主要通过 AR 基因扩增、突变和/或剪接变体重新激活 AR 信号。为了有效抑制重新激活的 AR 信号,目前正在积极探索针对 AR 的新方法。这些新方法包括靶向 AR 不同结构域的新型小分子抑制剂和可降解 AR 的药物。本综述概述了现有的经 FDA 批准的 AR 拮抗剂以及一些 AR 靶向药物目前的发展情况。
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Androgen receptor inhibitors in treating prostate cancer.

Abstract: Androgens play an important role in prostate cancer development and progression. Androgen action is mediated through the androgen receptor (AR), a ligand-dependent DNA-binding transcription factor. AR is arguably the most important target for prostate cancer treatment. Current USA Food and Drug Administration (FDA)-approved AR inhibitors target the ligand-binding domain (LBD) and have exhibited efficacy in prostate cancer patients, particularly when used in combination with androgen deprivation therapy. Unfortunately, patients treated with the currently approved AR-targeting agents develop resistance and relapse with castration-resistant prostate cancer (CRPC). The major mechanism leading to CRPC involves reactivation of AR signaling mainly through AR gene amplification, mutation, and/or splice variants. To effectively inhibit the reactivated AR signaling, new approaches to target AR are being actively explored. These new approaches include novel small molecule inhibitors targeting various domains of AR and agents that can degrade AR. The present review provides a summary of the existing FDA-approved AR antagonists and the current development of some of the AR targeting agents.

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