Metabolic dysfunction and cancer in HCV: Shared pathways and mutual interactions.
HCC
HCV
Hepatitis C virus
Hepatocellular carcinoma
metabolic dysfunction
senescence
steatosis
Journal
Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886
Informations de publication
Date de publication:
07 2022
07 2022
Historique:
received:
31
08
2021
revised:
12
01
2022
accepted:
31
01
2022
pubmed:
15
2
2022
medline:
22
6
2022
entrez:
14
2
2022
Statut:
ppublish
Résumé
HCV hijacks many host metabolic processes in an effort to aid viral replication. The resulting hepatic metabolic dysfunction underpins many of the hepatic and extrahepatic manifestations of chronic hepatitis C (CHC). However, the natural history of CHC is also substantially influenced by the host metabolic status: obesity, insulin resistance and hepatic steatosis are major determinants of CHC progression toward hepatocellular carcinoma (HCC). Direct-acting antivirals (DAAs) have transformed the treatment and natural history of CHC. While DAA therapy effectively eradicates the virus, the long-lasting overlapping metabolic disease can persist, especially in the presence of obesity, increasing the risk of liver disease progression. This review covers the mechanisms by which HCV tunes hepatic and systemic metabolism, highlighting how systemic metabolic disturbance, lipotoxicity and chronic inflammation favour disease progression and a precancerous niche. We also highlight the therapeutic implications of sustained metabolic dysfunction following sustained virologic response as well as considerations for patients who develop HCC on the background of metabolic dysfunction.
Identifiants
pubmed: 35157957
pii: S0168-8278(22)00076-9
doi: 10.1016/j.jhep.2022.01.029
pii:
doi:
Substances chimiques
Antiviral Agents
0
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
219-236Subventions
Organisme : Medical Research Council
ID : MR/R023026/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/K0019494/1
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C9380/A26813
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C18342/A23390
Pays : United Kingdom
Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Conflicts of interest D.A.M. is a director of Fibrofind limited. J.L. and D.A.M. are shareholders in Fibrofind limited. The other authors report no conflicts of interest. Please refer to the accompanying ICMJE disclosure forms for further details.