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HBV DNA Integration: Molecular Mechanisms and Clinical Implications

Chronic infection with the Hepatitis B Virus (HBV) is a major cause of liver-related morbidity and mortality. One peculiar observation in cells infected with HBV (or with closely‑related animal hepadnaviruses) is the presence of viral DNA integration in the host cell genome, despite this form being...

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Autores principales: Tu, Thomas, Budzinska, Magdalena A., Shackel, Nicholas A., Urban, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408681/
https://www.ncbi.nlm.nih.gov/pubmed/28394272
http://dx.doi.org/10.3390/v9040075
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author Tu, Thomas
Budzinska, Magdalena A.
Shackel, Nicholas A.
Urban, Stephan
author_facet Tu, Thomas
Budzinska, Magdalena A.
Shackel, Nicholas A.
Urban, Stephan
author_sort Tu, Thomas
collection PubMed
description Chronic infection with the Hepatitis B Virus (HBV) is a major cause of liver-related morbidity and mortality. One peculiar observation in cells infected with HBV (or with closely‑related animal hepadnaviruses) is the presence of viral DNA integration in the host cell genome, despite this form being a replicative dead-end for the virus. The frequent finding of somatic integration of viral DNA suggests an evolutionary benefit for the virus; however, the mechanism of integration, its functions, and the clinical implications remain unknown. Here we review the current body of knowledge of HBV DNA integration, with particular focus on the molecular mechanisms and its clinical implications (including the possible consequences of replication-independent antigen expression and its possible role in hepatocellular carcinoma). HBV DNA integration is likely to influence HBV replication, persistence, and pathogenesis, and so deserves greater attention in future studies.
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spelling pubmed-54086812017-05-18 HBV DNA Integration: Molecular Mechanisms and Clinical Implications Tu, Thomas Budzinska, Magdalena A. Shackel, Nicholas A. Urban, Stephan Viruses Review Chronic infection with the Hepatitis B Virus (HBV) is a major cause of liver-related morbidity and mortality. One peculiar observation in cells infected with HBV (or with closely‑related animal hepadnaviruses) is the presence of viral DNA integration in the host cell genome, despite this form being a replicative dead-end for the virus. The frequent finding of somatic integration of viral DNA suggests an evolutionary benefit for the virus; however, the mechanism of integration, its functions, and the clinical implications remain unknown. Here we review the current body of knowledge of HBV DNA integration, with particular focus on the molecular mechanisms and its clinical implications (including the possible consequences of replication-independent antigen expression and its possible role in hepatocellular carcinoma). HBV DNA integration is likely to influence HBV replication, persistence, and pathogenesis, and so deserves greater attention in future studies. MDPI 2017-04-10 /pmc/articles/PMC5408681/ /pubmed/28394272 http://dx.doi.org/10.3390/v9040075 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tu, Thomas
Budzinska, Magdalena A.
Shackel, Nicholas A.
Urban, Stephan
HBV DNA Integration: Molecular Mechanisms and Clinical Implications
title HBV DNA Integration: Molecular Mechanisms and Clinical Implications
title_full HBV DNA Integration: Molecular Mechanisms and Clinical Implications
title_fullStr HBV DNA Integration: Molecular Mechanisms and Clinical Implications
title_full_unstemmed HBV DNA Integration: Molecular Mechanisms and Clinical Implications
title_short HBV DNA Integration: Molecular Mechanisms and Clinical Implications
title_sort hbv dna integration: molecular mechanisms and clinical implications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408681/
https://www.ncbi.nlm.nih.gov/pubmed/28394272
http://dx.doi.org/10.3390/v9040075
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