Use of Protein Arginine Methyltransferase Inhibitors in Gliomas.

IF 5.6 2区 医学 Q1 ONCOLOGY
JCO precision oncology Pub Date : 2025-08-01 Epub Date: 2025-08-27 DOI:10.1200/PO-25-00518
Emirhan Harbi, Christopher E Mason
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引用次数: 0

Abstract

Gliomas are a type of CNS tumors. Protein arginine methyltransferases (PRMTs) play important epigenetic regulatory roles in various cancers, including gliomas, by regulating DNA repair and cellular signaling pathways. Recent studies have also identified overexpression of PRMTs in gliomas and have shown that it is associated with tumor progression and resistance to conventional therapies. Targeting PRMTs has shown promising preclinical results demonstrating the potential to disrupt tumor growth, enhance DNA damage responses, and improve the sensitivity of gliomas to radiotherapy and temozolomide. In this review, we focus on the translational and clinical relevance of PRMT inhibitors in glioma subtypes, highlighting their latest clinical developments and ongoing clinical trials. Unlike previous reviews, our article provides an updated synthesis of clinical data, discusses challenges and opportunities in clinical translation, and suggests future directions for integrating PRMT inhibitors into glioma therapy.

蛋白精氨酸甲基转移酶抑制剂在胶质瘤中的应用。
胶质瘤是一种中枢神经系统肿瘤。蛋白精氨酸甲基转移酶(PRMTs)通过调节DNA修复和细胞信号通路,在包括胶质瘤在内的多种癌症中发挥重要的表观遗传调控作用。最近的研究也发现了PRMTs在胶质瘤中的过表达,并表明它与肿瘤进展和对常规治疗的耐药性有关。靶向PRMTs已经显示出有希望的临床前结果,表明有可能破坏肿瘤生长,增强DNA损伤反应,并提高胶质瘤对放疗和替莫唑胺的敏感性。在这篇综述中,我们重点讨论了PRMT抑制剂在胶质瘤亚型中的转化和临床相关性,重点介绍了它们的最新临床进展和正在进行的临床试验。与之前的综述不同,我们的文章提供了最新的临床数据综合,讨论了临床转化的挑战和机遇,并提出了将PRMT抑制剂整合到胶质瘤治疗中的未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.10
自引率
4.30%
发文量
363
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