Src kinase as a potential therapeutic target in non-alcoholic and alcoholic steatohepatitis

Publons ID(not set)
Wos IDWOS:001288746200002
Doi10.1002/ctd2.18
TitleSrc kinase as a potential therapeutic target in non-alcoholic and alcoholic steatohepatitis
First Author
Last Author
AuthorsKurniawan, DW; Booijink, R; Jajoriya, AK; Dhawan, G; Mishra, D; Oosterhuis, D; Argemi, J; Storm, G; Olinga, P; Bataller, R; Mohanty, SK; Mishra, DP; Prakash, J; Bansal, R;
Publish DateMAR 2022
Journal NameCLINICAL AND TRANSLATIONAL DISCOVERY
Citation
AbstractNon-alcoholic steatohepatitis (NASH) and alcohol-associated steatohepatitis (ASH) are the major cause of liver-related mortality with limited therapeutic options available. In this study, we investigated the role of Src tyrosine kinase in the pathogenesis of (N)ASH. We examined Src kinase expression in livers from patients with NASH, ASH, cirrhosis and biliary atresia, and from preclinical mouse models: methionine choline deficient (MCD)-diet-induced NASH, Lieber-DeCarli ethanol (EtOH)-diet-induced ASH, carbon tetrachloride (CCl4)- and bile duct ligation (BDL)-induced liver fibrosis. Functional studies, using Src kinase inhibitor KX2-391, were performed in NASH and ASH mouse models, and in relevant in vitro models. Transcriptomic analysis revealed increased Src kinase expression in human and mouse diseased livers that positively correlated with disease progression. Src kinase inhibition ameliorated lipid biosynthesis (steatosis); monocytes/macrophages infiltration and inflammatory cytokines expression (inflammation) and hepatic stellate cells (HSCs) activation and collagen expression (fibrosis) in MCD-diet and EtOH-diet induced liver disease mouse models. In vitro Src inhibition attenuated FFA-induced hepatocytic lipid accumulation, LPS/IFN gamma-induced nitric oxide release and expression of several inflammatory signatures in macrophages and TGF beta-induced HSCs activation, contractility and collagen expression. Moreover, Src inhibition diminished gene expression of inflammatory markers in LPS/IFN gamma-stimulated BMDMs and LPS-stimulated PCLS, and reduced FA accumulation, macrophage activation and collagen deposition in 3D human liver spheroids. Mechanistic studies further revealed that Src kinase mediated the effects through FAK/PI3K/AKT pathway. Our results demonstrate a multicellular and functional role of Src kinase highlighting Src kinase as a promising therapeutic target in (non)alcoholic steatohepatitis.
Publish TypeJournal
Publish Year2022
Page Begin(not set)
Page End(not set)
Issn
Eissn2768-0622
Urlhttps://www.webofscience.com/wos/woscc/full-record/WOS:001288746200002
AuthorDr DHADHANG WAHYU KURNIAWAN, S.Si, M.Sc.
File162980.pdf