Viral non-coding RNA inhibits HNF4α expression in HCV associated hepatocellular carcinoma

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Wang, Zhao and Ceniccola, Kristin and Florea, Liliana and Wang, Bi-Dar and Lee, Norman H. and Kumar, Ajit (2015) Viral non-coding RNA inhibits HNF4α expression in HCV associated hepatocellular carcinoma. Infectious Agents and Cancer, 10. 19. ISSN 1750-9378 (https://doi.org/10.1186/s13027-015-0014-0)

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Abstract

Background Hepatitis C virus (HCV) infection is an established cause of chronic hepatitis, cirrhosis and hepatocellular carcinoma (HCC); however, it is unclear if the virus plays a direct role in the development of HCC. Hepatocyte nuclear factor 4α (HNF4α) is critical determinant of epithelial architecture and hepatic development; depletion of HNF4α is correlated with oncogenic transformation. We explored the viral role in the inhibition of HNF4α expression, and consequent induction of tumor-promoting genes in HCV infection-associated HCC. Methods Western blot analysis was used to monitor the changes in expression levels of oncogenic proteins in liver tissues from HCV-infected humanized mice. The mechanism of HNF4α depletion was studied in HCV-infected human hepatocyte cultures in vitro. Targeting of HNF4α expression by viral non-coding RNA was examined by inhibition of Luciferase HNF4α 3’-UTR reporter. Modulation of invasive properties of HCV-infected cells was examined by Matrigel cell migration assay. Results Results show inhibition of HNF4α expression by targeting of HNF4α 3’-UTR by HCV-derived small non-coding RNA, vmr11. Vmr11 enhances the invasive properties of HCV-infected cells. Loss of HNF4α in HCV-infected liver tumors of humanized mice correlates with the induction of epithelial to mesenchymal transition (EMT) genes. Conclusions We show depletion of HNF4α in liver tumors of HCV-infected humanized mice by HCV derived small non-coding RNA (vmr11) and resultant induction of EMT genes, which are critical determinants of tumor progression. These results suggest a direct viral role in the development of hepatocellular carcinoma.

ORCID iDs

Wang, Zhao, Ceniccola, Kristin ORCID logoORCID: https://orcid.org/0000-0002-2506-0750, Florea, Liliana, Wang, Bi-Dar, Lee, Norman H. and Kumar, Ajit;
CORE (COnnecting REpositories)