Abstract
Several microRNAs (miRNAs), including liver-specific miR-122, have been implicated in the control of hepatitis C virus (HCV) RNA replication and its response to interferon (IFN) in human hepatoma cells. Our analysis of liver biopsies from subjects with chronic hepatitis C (CHC) undergoing IFN therapy revealed no correlation of miR-122 expression with viral load and markedly decreased pretreatment miR-122 levels in subjects who had no virological response during later IFN therapy; other investigated miRNAs showed only limited changes. These data have implications for the prospect of targeting miRNAs for CHC therapy.
Publication types
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Clinical Trial
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Antiviral Agents / therapeutic use
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Biomarkers, Pharmacological / metabolism
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Cells, Cultured
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Down-Regulation / genetics
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Drug Resistance, Viral / genetics
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Hepatitis C / drug therapy*
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Hepatitis C / genetics
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Hepatitis C / metabolism
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Hepatitis C / pathology
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Humans
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Interferon-alpha / therapeutic use*
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Liver / metabolism
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Liver / pathology
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Liver / virology
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MicroRNAs / genetics*
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MicroRNAs / metabolism
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Treatment Failure
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Viral Load
Substances
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Antiviral Agents
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Biomarkers, Pharmacological
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Interferon-alpha
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MIRN122 microRNA, human
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MicroRNAs