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Liver Cell Transformation in Chronic HBV Infection

Epidemiological studies have provided overwhelming evidence for a causal role of chronic HBV infection in the development of hepatocellular carcinoma (HCC), but the molecular mechanisms underlying virally-induced tumorigenesis remain largely debated. In the absence of a dominant oncogene encoded by...

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Autores principales: Benhenda, Shirine, Cougot, Delphine, Neuveut, Christine, Buendia, Marie Annick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185520/
https://www.ncbi.nlm.nih.gov/pubmed/21994562
http://dx.doi.org/10.3390/v1030630
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author Benhenda, Shirine
Cougot, Delphine
Neuveut, Christine
Buendia, Marie Annick
author_facet Benhenda, Shirine
Cougot, Delphine
Neuveut, Christine
Buendia, Marie Annick
author_sort Benhenda, Shirine
collection PubMed
description Epidemiological studies have provided overwhelming evidence for a causal role of chronic HBV infection in the development of hepatocellular carcinoma (HCC), but the molecular mechanisms underlying virally-induced tumorigenesis remain largely debated. In the absence of a dominant oncogene encoded by the HBV genome, indirect roles have been proposed, including insertional activation of cellular oncogenes by HBV DNA integration, induction of genetic instability by viral integration or by the regulatory protein HBx, and long term effects of viral proteins in enhancing immune-mediated liver disease. In this chapter, we discuss different models of HBV-mediated liver cell transformation based on animal systems of hepadnavirus infection as well as functional studies in hepatocyte and hepatoma cell lines. These studies might help identifying the cellular effectors connecting HBV infection and liver cell transformation.
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spelling pubmed-31855202011-10-12 Liver Cell Transformation in Chronic HBV Infection Benhenda, Shirine Cougot, Delphine Neuveut, Christine Buendia, Marie Annick Viruses Article Epidemiological studies have provided overwhelming evidence for a causal role of chronic HBV infection in the development of hepatocellular carcinoma (HCC), but the molecular mechanisms underlying virally-induced tumorigenesis remain largely debated. In the absence of a dominant oncogene encoded by the HBV genome, indirect roles have been proposed, including insertional activation of cellular oncogenes by HBV DNA integration, induction of genetic instability by viral integration or by the regulatory protein HBx, and long term effects of viral proteins in enhancing immune-mediated liver disease. In this chapter, we discuss different models of HBV-mediated liver cell transformation based on animal systems of hepadnavirus infection as well as functional studies in hepatocyte and hepatoma cell lines. These studies might help identifying the cellular effectors connecting HBV infection and liver cell transformation. Molecular Diversity Preservation International (MDPI) 2009-10-30 /pmc/articles/PMC3185520/ /pubmed/21994562 http://dx.doi.org/10.3390/v1030630 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Benhenda, Shirine
Cougot, Delphine
Neuveut, Christine
Buendia, Marie Annick
Liver Cell Transformation in Chronic HBV Infection
title Liver Cell Transformation in Chronic HBV Infection
title_full Liver Cell Transformation in Chronic HBV Infection
title_fullStr Liver Cell Transformation in Chronic HBV Infection
title_full_unstemmed Liver Cell Transformation in Chronic HBV Infection
title_short Liver Cell Transformation in Chronic HBV Infection
title_sort liver cell transformation in chronic hbv infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185520/
https://www.ncbi.nlm.nih.gov/pubmed/21994562
http://dx.doi.org/10.3390/v1030630
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