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组蛋白去乙酰化酶抑制剂在肿瘤治疗中的进展:通过免疫调节的潜在应用

Advances of HDAC inhibitors in tumor therapy: potential applications through immune modulation.

作者信息

Tian Jiaqi, Han Miaomiao, Song Fuyang, Liu Yun, Shen Yuhou, Zhong Jiateng

机构信息

Department of Pathology, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, China.

Xinxiang Engineering Technology Research Center of Digestive Tumor Molecular Diagnosis, the First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.

出版信息

Front Oncol. 2025 Jun 27;15:1576781. doi: 10.3389/fonc.2025.1576781. eCollection 2025.

Abstract

Histone deacetylase inhibitors (HDAC inhibitors, HDACi) have garnered considerable attention due to their potential in treating various types of malignant tumors. Histone deacetylases (HDACs) not only influence chromatin structure and gene transcription by regulating histone acetylation status but also acetylate various non-histone proteins. They are widely involved in several key biological processes, such as cell cycle regulation, apoptosis induction, and immune responses. HDACi exert their effects by inhibiting HDAC activity; however, these effects are highly concentration-dependent and non-selective. HDACi inevitably disrupt both gene expression and signaling networks, leading to multi-target, non-specific biological effects. This article focuses on the immunomodulatory mechanisms of HDACi, including their role in remodeling the tumor extracellular matrix and their impact on various immune cell populations. The synergistic potential of combining HDACi with other therapeutic approaches is also discussed. This review examines the application of HDACi across different tumor types, highlighting preclinical and clinical evidence that demonstrates the multifunctionality and efficacy of HDACi. By leveraging their unique mechanism of action, HDACi opens new avenues for enhancing antitumor immunity and achieving durable therapeutic responses. Future research and clinical trials will play a crucial role in optimizing the use of HDACi, elucidating resistance mechanisms, and identifying the most effective combinations to maximize patient benefit.

摘要

组蛋白去乙酰化酶抑制剂(HDAC抑制剂,HDACi)因其在治疗各类恶性肿瘤方面的潜力而备受关注。组蛋白去乙酰化酶(HDACs)不仅通过调节组蛋白乙酰化状态影响染色质结构和基因转录,还能使多种非组蛋白乙酰化。它们广泛参与多个关键生物学过程,如细胞周期调控、凋亡诱导和免疫反应。HDACi通过抑制HDAC活性发挥作用;然而,这些作用高度依赖浓度且无选择性。HDACi不可避免地会扰乱基因表达和信号网络,导致多靶点、非特异性生物学效应。本文重点关注HDACi的免疫调节机制,包括它们在重塑肿瘤细胞外基质中的作用以及对各种免疫细胞群体的影响。还讨论了HDACi与其他治疗方法联合使用的协同潜力。本综述考察了HDACi在不同肿瘤类型中的应用,突出了临床前和临床证据,这些证据证明了HDACi的多功能性和有效性。通过利用其独特的作用机制,HDACi为增强抗肿瘤免疫力和实现持久治疗反应开辟了新途径。未来的研究和临床试验将在优化HDACi的使用、阐明耐药机制以及确定最有效的联合用药方案以最大化患者获益方面发挥关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3df4/12245688/1933955b2403/fonc-15-1576781-g001.jpg

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