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Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection

XMRV is a gammaretrovirus associated in some studies with human prostate cancer and chronic fatigue syndrome. Central to the hypothesis of XMRV as a human pathogen is the description of integration sites in DNA from prostate tumour tissues. Here we demonstrate that 2 of 14 patient-derived sites are...

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Detalles Bibliográficos
Autores principales: Garson, Jeremy A, Kellam, Paul, Towers, Greg J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050814/
https://www.ncbi.nlm.nih.gov/pubmed/21352548
http://dx.doi.org/10.1186/1742-4690-8-13
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author Garson, Jeremy A
Kellam, Paul
Towers, Greg J
author_facet Garson, Jeremy A
Kellam, Paul
Towers, Greg J
author_sort Garson, Jeremy A
collection PubMed
description XMRV is a gammaretrovirus associated in some studies with human prostate cancer and chronic fatigue syndrome. Central to the hypothesis of XMRV as a human pathogen is the description of integration sites in DNA from prostate tumour tissues. Here we demonstrate that 2 of 14 patient-derived sites are identical to sites cloned in the same laboratory from experimentally infected DU145 cells. Identical integration sites have never previously been described in any retrovirus infection. We propose that the patient-derived sites are the result of PCR contamination. This observation further undermines the notion that XMRV is a genuine human pathogen.
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spelling pubmed-30508142011-03-09 Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection Garson, Jeremy A Kellam, Paul Towers, Greg J Retrovirology Correspondence XMRV is a gammaretrovirus associated in some studies with human prostate cancer and chronic fatigue syndrome. Central to the hypothesis of XMRV as a human pathogen is the description of integration sites in DNA from prostate tumour tissues. Here we demonstrate that 2 of 14 patient-derived sites are identical to sites cloned in the same laboratory from experimentally infected DU145 cells. Identical integration sites have never previously been described in any retrovirus infection. We propose that the patient-derived sites are the result of PCR contamination. This observation further undermines the notion that XMRV is a genuine human pathogen. BioMed Central 2011-02-25 /pmc/articles/PMC3050814/ /pubmed/21352548 http://dx.doi.org/10.1186/1742-4690-8-13 Text en Copyright ©2011 Garson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Correspondence
Garson, Jeremy A
Kellam, Paul
Towers, Greg J
Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection
title Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection
title_full Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection
title_fullStr Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection
title_full_unstemmed Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection
title_short Analysis of XMRV integration sites from human prostate cancer tissues suggests PCR contamination rather than genuine human infection
title_sort analysis of xmrv integration sites from human prostate cancer tissues suggests pcr contamination rather than genuine human infection
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050814/
https://www.ncbi.nlm.nih.gov/pubmed/21352548
http://dx.doi.org/10.1186/1742-4690-8-13
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