Role and targeting of the AGC kinase family in pulmonary fibrosis (Review)

Exp Ther Med. 2024 Mar 8;27(5):190. doi: 10.3892/etm.2024.12478. eCollection 2024 May.

Abstract

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.

Keywords: cAMP-dependent protein kinase A; cGMP-dependent protein kinase G; epithelial cell; extracellular matrix; fibroblasts; phospholipid-dependent protein kinase C; pulmonary fibrosis.

Publication types

  • Review

Grants and funding

Funding: The present study was supported by grants from the National Natural Science Foundation of China (grant nos. 82060023 and 82160133) and the Jiangxi Provincial Natural Science Foundation (grant nos. 20202ACBL206015, 20224BAB206007 and 20212ACB216005).