Current and emerging pharmacotherapeutic interventions for the treatment of liver fibrosis.
Animals
Apoptosis
/ drug effects
Clinical Trials as Topic
Disease Progression
Drug Evaluation, Preclinical
Humans
Inflammation
Liver
/ drug effects
Liver Cirrhosis
/ drug therapy
Metabolic Networks and Pathways
/ drug effects
Molecular Targeted Therapy
Non-alcoholic Fatty Liver Disease
/ complications
Apoptosis
FXR
NAFLD
NASH
PPAR
gut-liver axis
hepatic stellate cell
molecular targets
myofibroblast
nuclear receptor
regression
Journal
Expert opinion on pharmacotherapy
ISSN: 1744-7666
Titre abrégé: Expert Opin Pharmacother
Pays: England
ID NLM: 100897346
Informations de publication
Date de publication:
Sep 2020
Sep 2020
Historique:
pubmed:
17
6
2020
medline:
15
9
2020
entrez:
17
6
2020
Statut:
ppublish
Résumé
Chronic liver disease is due to various causes of persistent liver damage and will eventually lead to the development of liver fibrosis. If no treatment is initiated, this condition may progress to cirrhosis and hepatocellular carcinoma. Current treatments comprise the elimination of the cause of injury, such as by lifestyle changes, alcohol abstinence, and antiviral agents. However, such etiology-driven therapy is often insufficient in patients with late-stage fibrosis/cirrhosis, therefore maintaining the need for efficient antifibrotic pharmacotherapeutic interventions. The authors discuss the recent advances in the development of antifibrotic drugs, which target various pathways of the fibrogenesis process, including cell death, inflammation, gut-liver axis, and myofibroblast activation. Due to the significant burden of nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH), various agents which specifically target metabolic pathways and their related receptors/ligands have been developed. For some of them, e.g., obeticholic acid, advanced stage clinical trials indicate antifibrotic efficacy in NAFLD and NASH. Significant advances have been made in the development of novel antifibrotic pharmacotherapeutics. The authors expect that the development of combinatorial therapies, which combine compounds that target various pathways of fibrosis progression, will have a major impact as future etiology-independent therapies.
Identifiants
pubmed: 32543284
doi: 10.1080/14656566.2020.1774553
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM