Department of Radiation and Medical Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Hubei Key Laboratory of Tumor Biological Behaviors, Zhongnan Hospital of Wuhan University, Wuhan, China.
Front Immunol. 2022 Apr 14;13:865964. doi: 10.3389/fimmu.2022.865964. eCollection 2022.
In recent years, protein arginine methyltransferases (PRMTs) have emerged as new members of a gene expression regulator family in eukaryotes, and are associated with cancer pathogenesis and progression. Cancer immunotherapy has significantly improved cancer treatment in terms of overall survival and quality of life. Protein arginine methylation is an epigenetic modification function not only in transcription, RNA processing, and signal transduction cascades, but also in many cancer-immunity cycle processes. Arginine methylation is involved in the activation of anti-cancer immunity and the regulation of immunotherapy efficacy. In this review, we summarize the most up-to-date information on regulatory molecular mechanisms and different underlying arginine methylation signaling pathways in innate and adaptive immune responses during cancer. We also outline the potential of PRMT-inhibitors as effective combinatorial treatments with immunotherapy.
近年来,蛋白精氨酸甲基转移酶(PRMTs)已成为真核生物基因表达调控家族的新成员,与癌症的发病机制和进展有关。癌症免疫疗法在整体生存率和生活质量方面显著改善了癌症治疗效果。蛋白质精氨酸甲基化是一种表观遗传修饰功能,不仅存在于转录、RNA 加工和信号转导级联中,也存在于许多癌症免疫周期过程中。精氨酸甲基化参与了抗癌免疫的激活和免疫治疗效果的调节。在这篇综述中,我们总结了关于癌症期间固有和适应性免疫反应中调节分子机制和不同潜在精氨酸甲基化信号通路的最新信息。我们还概述了 PRMT 抑制剂作为与免疫疗法相结合的有效联合治疗的潜力。