GSK-3 in liver diseases: Friend or foe?

Biochim Biophys Acta Mol Cell Res. 2020 Sep;1867(9):118743. doi: 10.1016/j.bbamcr.2020.118743. Epub 2020 May 15.

Abstract

Liver diseases, including hepatitis due to hepatitis B or C virus infection, non-alcoholic fatty liver disease, and hepatocellular carcinoma pose major challenges for overall health due to limited curative treatment options. Thus, there is an urgent need to develop new therapeutic strategies for the treatment of these diseases. A better understanding of the signaling pathways involved in the pathogenesis of liver diseases can help to improve the efficacy of emerging therapies, mainly based on pharmacological approaches, which influence one or more specific molecules involved in key signal transduction pathways. These emerging therapies are very promising for the prevention and treatment of liver diseases. One promising druggable molecular target is the multifunctional serine/threonine kinase, glycogen synthase kinase 3 (GSK-3). In this review, we discuss conditions in which GSK-3 is implicated in liver diseases. In addition, we explore newly emerging drugs that target GSK-3β, as well as their potential use in and impact on the management of liver diseases.

Keywords: Glycogen synthase kinase 3 (GSK-3); Hepatitis B virus (HBV); Hepatitis C virus (HCV); Hepatocellular carcinoma (HCC); Non-alcoholic fatty liver disease (NAFLD); Signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Disease Management
  • Disease Susceptibility*
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use
  • Gene Expression Regulation
  • Glycogen Synthase Kinase 3 / antagonists & inhibitors
  • Glycogen Synthase Kinase 3 / genetics*
  • Glycogen Synthase Kinase 3 / metabolism*
  • Host-Pathogen Interactions / genetics
  • Humans
  • Liver Diseases / drug therapy
  • Liver Diseases / etiology*
  • Liver Diseases / metabolism*
  • Liver Diseases / pathology
  • Molecular Targeted Therapy
  • Multigene Family
  • Signal Transduction

Substances

  • Biomarkers
  • Enzyme Inhibitors
  • Glycogen Synthase Kinase 3