Huang Jiezuo, Qiao Beining, Yuan Yixin, Xie Yuxuan, Xia Xiaomeng, Li Fenghe, Wang Lei
College of Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.
Xiangya College of Public Health, Central South University, Changsha, China.
J Cell Mol Med. 2025 Feb;29(4):e70386. doi: 10.1111/jcmm.70386.
The family of protein arginine methyltransferases (PRMTs) occupies an important position in biology, especially during the initiation and development of cancer. PRMT3 and CARM1(also known as PRMT4), being type I protein arginine methyltransferases, are key in controlling tumour progression by catalysing the mono-methylation and asymmetric di-methylation of both histone and non-histone substrates. This paper reviews the functions and potential therapeutic target value of PRMT3 and CARM1 in a variety of cancers. Studies have identified abnormal expressions of PRMT3 and CARM1 in several malignancies, closely linked to cancer progression, advancement, and resistance to treatment. Such as hepatocellular carcinoma, colorectal cancer, ovarian cancer, and endometrial cancer. These findings offer new strategies and directions for cancer treatment, especially in enhancing the effectiveness of conventional treatment methods.
蛋白质精氨酸甲基转移酶(PRMTs)家族在生物学中占据重要地位,尤其是在癌症的发生和发展过程中。PRMT3和CARM1(也称为PRMT4)作为I型蛋白质精氨酸甲基转移酶,通过催化组蛋白和非组蛋白底物的单甲基化和不对称二甲基化,在控制肿瘤进展中起关键作用。本文综述了PRMT3和CARM1在多种癌症中的功能及潜在治疗靶点价值。研究已确定PRMT3和CARM1在几种恶性肿瘤中表达异常,这与癌症进展、恶化及治疗耐药性密切相关。如肝细胞癌、结直肠癌、卵巢癌和子宫内膜癌。这些发现为癌症治疗提供了新策略和方向,特别是在提高传统治疗方法的有效性方面。