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靶向组蛋白去乙酰化酶的表观遗传调节剂在癌症免疫治疗中的应用。

HDAC-targeting epigenetic modulators for cancer immunotherapy.

机构信息

School of Medicine, Hubei Polytechnic University, Huangshi, 435003, PR China; Key Laboratory of Joint Diagnosis and Treatment of Chronic Liver Disease and Liver Cancer of Lishui, The Sixth Affiliated Hospital of Wenzhou Medical University, Lishui People's Hospital, Lishui, Zhejiang, 323000, PR China; Molecular Pharmacology Research Center, School of Pharmaceutical Science, Wenzhou Medical University, Wenzhou, 325035, PR China.

CardioIogy Department, Geriatric Department, Foshan Women and Children Hospital, Foshan, Guangdong, 528000, PR China.

出版信息

Eur J Med Chem. 2024 Feb 5;265:116129. doi: 10.1016/j.ejmech.2024.116129. Epub 2024 Jan 6.

Abstract

HDAC inhibitors, which can inhibit the activity of HDAC enzymes, have been extensively studied in tumor immunotherapy and have shown potential therapeutic effects in cancer immunotherapy. To date, numerous small molecule HDAC inhibitors have been identified, but many of them suffer from limited clinical efficacy and serious toxicity. Hence, HDAC inhibitor-based combination therapies, and other HDAC modulators (e.g. PROTAC degraders, dual-acting agents) have attracted great attention with significant advancements achieved in the past few years due to their superior efficacy compared to single-target HDAC inhibitors. In this review, we overviewed the recent progress on HDAC-based drug discovery with a focus on HDAC inhibitor-based drug combination therapy and other HDAC-targeting strategies (e.g. selective HDAC inhibitors, HDAC-based dual-target inhibitors, and PROTAC HDAC degraders) for cancer immunotherapy. In addition, we also summarized the reported co-crystal structures of HDAC inhibitors in complex with their target proteins and the binding interactions. Finally, the challenges and future directions for HDAC-based drug discovery in cancer immunotherapy are also discussed in detail.

摘要

组蛋白去乙酰化酶抑制剂可抑制组蛋白去乙酰化酶酶的活性,在肿瘤免疫治疗中得到了广泛的研究,并在癌症免疫治疗中显示出潜在的治疗效果。迄今为止,已经鉴定出许多小分子组蛋白去乙酰化酶抑制剂,但其中许多抑制剂由于临床疗效有限和严重的毒性而受到限制。因此,基于组蛋白去乙酰化酶抑制剂的联合治疗以及其他组蛋白去乙酰化酶调节剂(例如 PROTAC 降解剂、双作用剂)引起了极大的关注,由于与单靶标组蛋白去乙酰化酶抑制剂相比具有更好的疗效,近年来在这方面取得了显著进展。在这篇综述中,我们综述了基于组蛋白去乙酰化酶的药物发现的最新进展,重点介绍了基于组蛋白去乙酰化酶抑制剂的药物联合治疗以及其他组蛋白去乙酰化酶靶向策略(例如选择性组蛋白去乙酰化酶抑制剂、基于组蛋白去乙酰化酶的双靶标抑制剂和 PROTAC 组蛋白去乙酰化酶降解剂)在癌症免疫治疗中的应用。此外,我们还总结了报道的组蛋白去乙酰化酶抑制剂与靶蛋白的共晶体结构以及结合相互作用。最后,还详细讨论了基于组蛋白去乙酰化酶的药物发现在癌症免疫治疗中的挑战和未来方向。

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