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雄激素受体抑制剂在前列腺癌治疗中的应用

Androgen receptor inhibitors in treating prostate cancer.

作者信息

Cole Ryan N, Fang Qinghua, Matsuoka Kanako, Wang Zhou

机构信息

Department of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15232, USA.

UPMC Hillman Cancer Center, University of Pittsburgh School of Medicine, Pittsburgh, PA 15232, USA.

出版信息

Asian J Androl. 2025 Mar 1;27(2):144-155. doi: 10.4103/aja202494. Epub 2024 Nov 19.

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.

摘要

雄激素在前列腺癌的发生和发展中起着重要作用。雄激素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。AR可以说是前列腺癌治疗的最重要靶点。目前美国食品药品监督管理局(FDA)批准的AR抑制剂作用于配体结合域(LBD),并已在前列腺癌患者中显示出疗效,尤其是与雄激素剥夺疗法联合使用时。不幸的是,接受目前批准的AR靶向药物治疗的患者会产生耐药性,并复发为去势抵抗性前列腺癌(CRPC)。导致CRPC的主要机制涉及AR信号的重新激活,主要是通过AR基因扩增、突变和/或剪接变体。为了有效抑制重新激活的AR信号,人们正在积极探索靶向AR的新方法。这些新方法包括靶向AR各个结构域的新型小分子抑制剂和能够降解AR的药物。本综述总结了现有的FDA批准的AR拮抗剂以及一些AR靶向药物的当前研发情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a1e/11949463/752f27cc529e/AJA-27-144-g001.jpg

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