Chen Ting, Liu Jinxin, Li Shizhe, Wang Peter, Shang Guanning
Department of Orthopedics, Shengjing Hospital of China Medical University, Shenyang, Liaoning 110004, China.
Bengbu Medical College Key Laboratory of Cancer Research and Clinical Laboratory Diagnosis, Department of Biochemistry and Molecular Biology, School of Laboratory Medicine, Bengbu Medical College, Anhui 233030, China.
Semin Cell Dev Biol. 2024 Feb 15;154(Pt C):208-214. doi: 10.1016/j.semcdb.2022.08.005. Epub 2022 Sep 6.
Protein arginine methyltransferases (PRMTs) promote the methylation of numerous proteins at their arginine residues. An increasing number of publications have suggested that dysregulation of PRMTs participates in various human diseases, such as cardiovascular diseases, cancer, diabetes and neurodegenerative disorders. Inflammation is one normal response to infection or injury by immune system, which can keep body homeostasis. Emerging data reveal that inflammation is associated with the development of numerous diseases. Moreover, accumulated evidence proves that PRMTs have been characterized to regulate inflammation in various diseases. In this review article, we delineate the function and molecular mechanism of PRMTs in regulation of inflammation in current literature. Moreover, we discuss that targeting PRMTs by its inhibitors and compounds could have therapeutic potential.
蛋白质精氨酸甲基转移酶(PRMTs)可促进多种蛋白质的精氨酸残基发生甲基化。越来越多的出版物表明,PRMTs的失调参与了各种人类疾病,如心血管疾病、癌症、糖尿病和神经退行性疾病。炎症是免疫系统对感染或损伤的一种正常反应,可维持身体的稳态。新出现的数据表明,炎症与多种疾病的发生发展有关。此外,越来越多的证据证明,PRMTs在多种疾病中已被证实可调节炎症。在这篇综述文章中,我们阐述了当前文献中PRMTs在炎症调节中的功能和分子机制。此外,我们还讨论了通过其抑制剂和化合物靶向PRMTs可能具有治疗潜力。