Publication:
Mouse DNA contamination in human tissue tested for XMRV

dc.contributor.authorMark J. Robinsonen_US
dc.contributor.authorOtto W. Erlweinen_US
dc.contributor.authorSteve Kayeen_US
dc.contributor.authorJonathan Weberen_US
dc.contributor.authorOya Cingozen_US
dc.contributor.authorAnup Patelen_US
dc.contributor.authorMarjorie M. Walkeren_US
dc.contributor.authorWun Jae Kimen_US
dc.contributor.authorMongkol Uiprasertkulen_US
dc.contributor.authorJohn M. Coffinen_US
dc.contributor.authorMyra O. McClureen_US
dc.contributor.otherImperial College Londonen_US
dc.contributor.otherTufts Universityen_US
dc.contributor.otherSt Mary's Hospital Londonen_US
dc.contributor.otherChungbuk National University, College of Medicineen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-24T09:03:22Z
dc.date.available2018-09-24T09:03:22Z
dc.date.issued2010-12-20en_US
dc.description.abstractBackground: We used a PCR-based approach to study the prevalence of genetic sequences related to a gammaretrovirus, xenotropic murine leukemia virus-related virus, XMRV, in human prostate cancer. This virus has been identified in the US in prostate cancer patients and in those with chronic fatigue syndrome. However, with the exception of two patients in Germany, XMRV has not been identified in prostate cancer tissue in Europe. Most putative associations of new or old human retroviruses with diseases have turned out to be due to contamination. We have looked for XMRV sequences in DNA extracted from formalin-fixed paraffin- embedded prostate tissues. To control for contamination, PCR assays to detect either mouse mitochondrial DNA (mtDNA) or intracisternal A particle (IAP) long terminal repeat DNA were run on all samples, owing to their very high copy number in mouse cells.Results: In general agreement with the US prevalence, XMRV-like sequences were found in 4.8% of prostate cancers. However, these were also positive, as were 21.5% of XMRV-negative cases, for IAP sequences, and many, but not all were positive for mtDNA sequences.Conclusions: These results show that contamination with mouse DNA is widespread and detectable by the highly sensitive IAP assay, but not always with less sensitive assays, such as murine mtDNA PCR. This study highlights the ubiquitous presence of mouse DNA in laboratory specimens and offers a means of rigorous validation for future studies of murine retroviruses in human disease. © 2010 Robinson et al; licensee BioMed Central Ltd.en_US
dc.identifier.citationRetrovirology. Vol.7, (2010)en_US
dc.identifier.doi10.1186/1742-4690-7-108en_US
dc.identifier.issn17424690en_US
dc.identifier.other2-s2.0-78650299460en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/29151
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650299460&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleMouse DNA contamination in human tissue tested for XMRVen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=78650299460&origin=inwarden_US

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