Targeting type I PRMTs as promising targets for the treatment of pulmonary disorders: Asthma, COPD, lung cancer, PF, and PH

被引:1
作者
Zhou, Shuyan [1 ,2 ]
Zhang, Qiangsheng [1 ,2 ]
Yang, Honglin [1 ,2 ]
Zhu, Yongxia [3 ]
Hu, Xiang [1 ,2 ]
Wan, Guoquan [1 ,2 ]
Yu, Luoting [1 ,2 ]
机构
[1] Sichuan Univ, Canc Ctr, Dept Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[3] Univ Elect Sci & Technol China, Sichuan Canc Hosp & Inst, Sichuan Canc Ctr, Sch Med,Dept Pharm, Chengdu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Epigenetics; Asthma; COPD; Lung cancer; Pulmonary fibrosis; Pulmonary hypertension; Type I PRMTs; ARGININE METHYLTRANSFERASE 1; ACTIVE ALLOSTERIC INHIBITOR; ASYMMETRIC DIMETHYLARGININE; ACUTE EXACERBATION; STRUCTURAL BASIS; NITRIC-OXIDE; POTENT; CARM1; EXPRESSION; DISCOVERY;
D O I
10.1016/j.lfs.2024.122538
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Pulmonary disorders, including asthma, chronic obstructive pulmonary disease (COPD), pulmonary fibrosis (PF), pulmonary hypertension (PH), and lung cancer, seriously impair the quality of lives of patients. A deeper understanding of the occurrence and development of the above diseases may inspire new strategies to remedy the scarcity of treatments. Type I protein arginine methyltransferases (PRMTs) can affect processes of inflammation, airway remodeling, fibroblast proliferation, mitochondrial mass, and epithelial dysfunction through substrate methylation and non-enzymatic activity, thus affecting the occurrence and development of asthma, COPD, lung cancer, PF, and PH. As potential therapeutic targets, inhibitors of type I PRMTs are developed, moreover, representative compounds such as GSK3368715 and MS023 have also been used for early research. Here, we collated structures of type I PRMTs inhibitors and compared their activity. Finally, we highlighted the physiological and pathological associations of type I PRMTs with asthma, COPD, lung cancer, PF, and PH. The developing of type I PRMTs modulators will be beneficial for the treatment of these diseases.
引用
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页数:14
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