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靶向“不可成药”靶点:增殖细胞核抗原(PCNA)小分子抑制剂在癌症治疗中备受关注

Targeting the "Undruggable": Small-Molecule Inhibitors of Proliferating Cell Nuclear Antigen (PCNA) in the Spotlight in Cancer Therapy.

作者信息

Wang Tiantian, Wang Zengtao

机构信息

College of Pharmacy, Jiangxi University of Chinese Medicine, Nanchang 330004, P. R. China.

National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang 330006, P. R. China.

出版信息

J Med Chem. 2025 Feb 13;68(3):2058-2088. doi: 10.1021/acs.jmedchem.4c00526. Epub 2025 Feb 4.

Abstract

PCNA plays multiple roles in cancer development, including cell proliferation regulation, DNA repair, replication, and serving as a widely used biomarker and therapeutic target. Despite its significant role in oncology, PCNA has historically been considered "undruggable" due to the absence of known endogenous small molecule modulators and identifiable ligand binding sites. Unlike other protein-protein interfaces, PCNA lacks explicit binding grooves, featuring a relatively small and shallow surface pocket, which hinders the discovery of traditional small molecule targets. Recent breakthroughs have introduced promising PCNA-targeting candidates, with and entering phase I clinical trials for cancer therapy, garnering academic and industry interest. These achievements provide new evidence for PCNA as a drug target. This article provides insight and perspective on the application of small-molecule PCNA inhibitors in cancer treatment, covering PCNA function, its relationship with cancer, structural modification of small molecule inhibitors, and discovery strategies.

摘要

增殖细胞核抗原(PCNA)在癌症发展中发挥多种作用,包括细胞增殖调控、DNA修复、复制,并且作为一种广泛使用的生物标志物和治疗靶点。尽管PCNA在肿瘤学中具有重要作用,但由于缺乏已知的内源性小分子调节剂和可识别的配体结合位点,它在历史上一直被认为“难以成药”。与其他蛋白质-蛋白质界面不同,PCNA缺乏明确的结合凹槽,其表面口袋相对较小且较浅,这阻碍了传统小分子靶点的发现。最近的突破引入了有前景的靶向PCNA的候选药物,其中[具体药物1]和[具体药物2]已进入癌症治疗的I期临床试验,引起了学术界和产业界的兴趣。这些成果为PCNA作为药物靶点提供了新证据。本文提供了关于小分子PCNA抑制剂在癌症治疗中的应用的见解和观点,涵盖PCNA功能、其与癌症的关系、小分子抑制剂的结构修饰以及发现策略。

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