Publication: Metabolic dysfunction and cancer in HCV: shared pathways and mutual interactions
dc.contributor.coauthor | Leslie, Jack | |
dc.contributor.coauthor | Geh, Daniel | |
dc.contributor.coauthor | Elsharkawy, Ahmed M. | |
dc.contributor.coauthor | Vacca, Michele | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Mann, Derek Austin | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2024-11-09T22:59:32Z | |
dc.date.issued | 2022 | |
dc.description.abstract | 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. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 1 | |
dc.description.openaccess | YES | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.sponsorship | UK Medical Research Council [MR/K0019494/1, MR/R023026/1] | |
dc.description.sponsorship | CRUK program [C9380/A26813, C18342/A23390] | |
dc.description.sponsorship | Newcastle CRUK Clinical Academic Training Programme JL, DG and DAM are supported by UK Medical Research Council program grants MR/K0019494/1, MR/R023026/1 and CRUK program grants (C9380/A26813) and (C18342/A23390) . DG is funded by the Newcastle CRUK Clinical Academic Training Programme. | |
dc.description.volume | 77 | |
dc.identifier.doi | 10.1016/j.jhep.2022.01.029 | |
dc.identifier.eissn | 1600-0641 | |
dc.identifier.issn | 0168-8278 | |
dc.identifier.quartile | Q1 | |
dc.identifier.scopus | 2-s2.0-85127356304 | |
dc.identifier.uri | https://doi.org/10.1016/j.jhep.2022.01.029 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/7908 | |
dc.identifier.wos | 833420900006 | |
dc.keywords | Hepatitis C Virus | |
dc.keywords | HCV | |
dc.keywords | Hepatocellular carcinoma | |
dc.keywords | Hcc metabolic dysfunction | |
dc.keywords | Steatosis | |
dc.keywords | Senescence | |
dc.keywords | Chronic Hepatitis-C | |
dc.keywords | Fatty liver-disease | |
dc.keywords | Virus core protein | |
dc.keywords | Hepatocellular-carcinoma patients | |
dc.keywords | Triglyceride transfer protein | |
dc.keywords | Endoplasmic-reticulum stress | |
dc.keywords | Type-2 diabetes-mellitus | |
dc.keywords | Body-mass index | |
dc.keywords | Insulin-resistance | |
dc.keywords | Oxidative stress | |
dc.language.iso | eng | |
dc.publisher | Elsevier | |
dc.relation.ispartof | Journal of Hepatology | |
dc.subject | Gastroenterology | |
dc.subject | Hepatology | |
dc.title | Metabolic dysfunction and cancer in HCV: shared pathways and mutual interactions | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Mann, Derek Austin | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
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relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
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