HCV core protein-induced down-regulation of microRNA-152 promoted aberrant proliferation by regulating Wnt1 in HepG2 cells.

HCV core protein-induced down-regulation of microRNA-152 promoted aberrant proliferation by regulating Wnt1 in HepG2 cells.

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BackgroundHepatitis C virus (HCV) psithurisme has been reported to regulate cellular microRNAs (miRNAs).The HCV core protein is considered to be a potential oncoprotein in HCV-related hepatocellular carcinoma (HCV-HCC), but HCV core-regulated miRNAs are largely unknown.Our preliminary experiments revealed significant down-regulation of microRNA-152 (miR-152) by HCV core protein in HepG2 cells.Through target gene prediction softwares, Wnt1 was predicted to be a potential target of miR-152.The present study was initiated to investigate whether miR-152 is aberrantly regulated by the HCV core protein, and involved in the regulation of the aberrant proliferation of HCV-HCC cells.

MethodsMiR-152 levels were examined by stem-loop real-time RT-PCR (SLqRT-PCR).Cell proliferation was analyzed by MTT and colony formation assay.Cell cycle analysis was performed by flow cytometry.Luciferase reporter assay was conducted to confirm miRNA-target association.Wnt1 tanguray covington expression was determined by real-time qPCR and Western blotting.

ResultsHCV core protein significantly suppressed miR-152 expression, and led to significant Wnt1 up-regulation with a concomitant aberrantly promoted proliferation.Moreover, we validated that miR-152 inhibition promoted, while miR-152 mimics inhibited cell proliferation.Using, qRT-PCR and western blot, Wnt1 was demonstrated to be regulated by miR-152.Luciferase activity assay showed that while miR-152 mimics significantly reduced the luciferase activity by 83.76% (PConclusionThese findings provide important evidence that the reduced miR-152 expression by HCV core protein can indirectly lose an inhibitory effect on Wnt1, which might, at least partially lead to cell proliferation of liver cancer cells.

MiR-152 may have a therapeutic potential to suppress liver cancer proliferation.