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The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors

Human bocavirus is the second autonomous human parvovirus with assumed pathogenic potential. Other parvoviruses are known to persist and even integrate into the host genome, eventually contributing to the multi-step development of cancer. Human bocavirus also persists in an unknown percentage of cli...

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Autores principales: Schildgen, Verena, Malecki, Monika, Tillmann, Ramona-Liza, Brockmann, Michael, Schildgen, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694905/
https://www.ncbi.nlm.nih.gov/pubmed/23826357
http://dx.doi.org/10.1371/journal.pone.0068020
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author Schildgen, Verena
Malecki, Monika
Tillmann, Ramona-Liza
Brockmann, Michael
Schildgen, Oliver
author_facet Schildgen, Verena
Malecki, Monika
Tillmann, Ramona-Liza
Brockmann, Michael
Schildgen, Oliver
author_sort Schildgen, Verena
collection PubMed
description Human bocavirus is the second autonomous human parvovirus with assumed pathogenic potential. Other parvoviruses are known to persist and even integrate into the host genome, eventually contributing to the multi-step development of cancer. Human bocavirus also persists in an unknown percentage of clinically asymptomatic patients in addition to those with primary infection. The aim of the present study was to analyze the role of Human bocavirus in lung and colorectal cancers. Therefore, formalin-fixed, paraffin-embedded, archived tumor samples were screened for Human bocavirus DNA by PCR, Southern blotting, and sequencing. Positive tissues were further subjected to fluorescence in situ hybridization analysis to specifically detect human bocavirus DNA in the infected cells. In total, 11 of the 60 (18.3%) lung and 9 of the 44 (20.5%) colorectal tumors tested positive for human bocavirus DNA by PCR and were confirmed by sequencing and fluorescence in situ hybridization analysis. Thus, human bocavirus DNA is present in the nuclei of infected cells, in either single or multiple copies, and appears to form concatemers. The occurrence of these human bocavirus DNA structures supports the existence of the postulated σ- or rolling-hairpin replication mechanism. Moreover, the fluorescence in situ hybridization patterns inspired the hypothesis that human bocavirus DNA either persists as cccDNA or is integrated into the host genome. This finding suggests that this virus may indirectly contribute to the development of some colorectal and lung cancers, as do other DNA viruses, such as the human hepatitis B virus, or may play an active role in cancer by interacting with the host genome.
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spelling pubmed-36949052013-07-03 The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors Schildgen, Verena Malecki, Monika Tillmann, Ramona-Liza Brockmann, Michael Schildgen, Oliver PLoS One Research Article Human bocavirus is the second autonomous human parvovirus with assumed pathogenic potential. Other parvoviruses are known to persist and even integrate into the host genome, eventually contributing to the multi-step development of cancer. Human bocavirus also persists in an unknown percentage of clinically asymptomatic patients in addition to those with primary infection. The aim of the present study was to analyze the role of Human bocavirus in lung and colorectal cancers. Therefore, formalin-fixed, paraffin-embedded, archived tumor samples were screened for Human bocavirus DNA by PCR, Southern blotting, and sequencing. Positive tissues were further subjected to fluorescence in situ hybridization analysis to specifically detect human bocavirus DNA in the infected cells. In total, 11 of the 60 (18.3%) lung and 9 of the 44 (20.5%) colorectal tumors tested positive for human bocavirus DNA by PCR and were confirmed by sequencing and fluorescence in situ hybridization analysis. Thus, human bocavirus DNA is present in the nuclei of infected cells, in either single or multiple copies, and appears to form concatemers. The occurrence of these human bocavirus DNA structures supports the existence of the postulated σ- or rolling-hairpin replication mechanism. Moreover, the fluorescence in situ hybridization patterns inspired the hypothesis that human bocavirus DNA either persists as cccDNA or is integrated into the host genome. This finding suggests that this virus may indirectly contribute to the development of some colorectal and lung cancers, as do other DNA viruses, such as the human hepatitis B virus, or may play an active role in cancer by interacting with the host genome. Public Library of Science 2013-06-27 /pmc/articles/PMC3694905/ /pubmed/23826357 http://dx.doi.org/10.1371/journal.pone.0068020 Text en © 2013 Schildgen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schildgen, Verena
Malecki, Monika
Tillmann, Ramona-Liza
Brockmann, Michael
Schildgen, Oliver
The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors
title The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors
title_full The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors
title_fullStr The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors
title_full_unstemmed The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors
title_short The Human Bocavirus Is Associated with Some Lung and Colorectal Cancers and Persists in Solid Tumors
title_sort human bocavirus is associated with some lung and colorectal cancers and persists in solid tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694905/
https://www.ncbi.nlm.nih.gov/pubmed/23826357
http://dx.doi.org/10.1371/journal.pone.0068020
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