Mei Chao, Chen Tao, Huang Xiangfei, Xiong Chenlu, Chen Shibiao, Li Yong
Department of Anesthesiology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Exp Ther Med. 2024 Mar 8;27(5):190. doi: 10.3892/etm.2024.12478. eCollection 2024 May.
Pulmonary fibrosis (PF) is a progressive and irreversible pulmonary disease with a high mortality rate and limited treatment options. The cAMP-dependent protein kinase A, cGMP-dependent protein kinase G and phospholipid-dependent protein kinase C, collectively known as AGC kinases, are evolutionarily conserved protein kinases that are widely distributed among eukaryotes. AGC kinases serve a crucial role in a variety of cellular functions and pathological processes, including cancer, diabetes, inflammation and viral infections, where they have been implicated the pathogenesis of PF. The present review summarizes the evidence for the involvement of specific AGC kinases in the pathogenesis of PF, and provides a theoretical basis for the development of targeted AGC kinase small molecule inhibitors or targeted drugs, offering more effective treatment options and strategies for patients with PF.
肺纤维化(PF)是一种进行性且不可逆的肺部疾病,死亡率高且治疗选择有限。环磷酸腺苷(cAMP)依赖性蛋白激酶A、环磷酸鸟苷(cGMP)依赖性蛋白激酶G和磷脂依赖性蛋白激酶C统称为AGC激酶,是进化上保守的蛋白激酶,广泛分布于真核生物中。AGC激酶在多种细胞功能和病理过程中起关键作用,包括癌症、糖尿病、炎症和病毒感染,它们与PF的发病机制有关。本综述总结了特定AGC激酶参与PF发病机制的证据,并为开发靶向AGC激酶的小分子抑制剂或靶向药物提供理论基础,为PF患者提供更有效的治疗选择和策略。