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    Metabolic dysfunction and cancer in HCV: Shared pathways and mutual interactions.

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    Author
    Leslie, Jack
    Geh, Daniel
    Elsharkawy, Ahmed M
    Mann, Derek A
    Vacca, Michele
    Publication date
    2022-02-12
    Subject
    Oncology. Pathology.
    
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    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.
    Citation
    Leslie J, Geh D, Elsharkawy AM, Mann DA, Vacca M. Metabolic dysfunction and cancer in HCV: Shared pathways and mutual interactions. J Hepatol. 2022 Jul;77(1):219-236. doi: 10.1016/j.jhep.2022.01.029. Epub 2022 Feb 12
    Type
    Article
    Handle
    http://hdl.handle.net/20.500.14200/2378
    Additional Links
    http://www.sciencedirect.com/science/journal/01688278
    DOI
    10.1016/j.jhep.2022.01.029
    PMID
    35157957
    Journal
    Journal of Hepatology
    Publisher
    Elsevier
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.jhep.2022.01.029
    Scopus Count
    Collections
    Gastroenterology

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