Publication:
Metabolic dysfunction and cancer in HCV: shared pathways and mutual interactions

dc.contributor.coauthorLeslie, Jack
dc.contributor.coauthorGeh, Daniel
dc.contributor.coauthorElsharkawy, Ahmed M.
dc.contributor.coauthorVacca, Michele
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorMann, Derek Austin
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T22:59:32Z
dc.date.issued2022
dc.description.abstractHCV 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.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue1
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipUK Medical Research Council [MR/K0019494/1, MR/R023026/1]
dc.description.sponsorshipCRUK program [C9380/A26813, C18342/A23390]
dc.description.sponsorshipNewcastle 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.volume77
dc.identifier.doi10.1016/j.jhep.2022.01.029
dc.identifier.eissn1600-0641
dc.identifier.issn0168-8278
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85127356304
dc.identifier.urihttps://doi.org/10.1016/j.jhep.2022.01.029
dc.identifier.urihttps://hdl.handle.net/20.500.14288/7908
dc.identifier.wos833420900006
dc.keywordsHepatitis C Virus
dc.keywordsHCV
dc.keywordsHepatocellular carcinoma
dc.keywordsHcc metabolic dysfunction
dc.keywordsSteatosis
dc.keywordsSenescence
dc.keywordsChronic Hepatitis-C
dc.keywordsFatty liver-disease
dc.keywordsVirus core protein
dc.keywordsHepatocellular-carcinoma patients
dc.keywordsTriglyceride transfer protein
dc.keywordsEndoplasmic-reticulum stress
dc.keywordsType-2 diabetes-mellitus
dc.keywordsBody-mass index
dc.keywordsInsulin-resistance
dc.keywordsOxidative stress
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofJournal of Hepatology
dc.subjectGastroenterology
dc.subjectHepatology
dc.titleMetabolic dysfunction and cancer in HCV: shared pathways and mutual interactions
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorMann, Derek Austin
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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