Contamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinoma

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Ciencias Forenses, Anatomía Patolóxica, Xinecoloxía e Obstetricia, e Pediatríagl
dc.contributor.authorBandelt, Hans-Jürgen
dc.contributor.authorSalas Ellacuriaga, Antonio
dc.date.accessioned2020-06-02T16:09:37Z
dc.date.available2020-06-02T16:09:37Z
dc.date.issued2009
dc.description.abstractThe study of somatic DNA instabilities constitutes a debatable topic because different causes can lead to seeming DNA alteration patterns between different cells or tissues from the same individual. Carcinogenesis or the action of a particular toxic could generate such patterns, and this is in fact the leitmotif of a number of studies on mitochondrial DNA (mtDNA) instability. Patterns of seeming instabilities could also arise from technical errors at any stage of the analysis (DNA extraction, amplification, mutation screening/sequencing, and documentation). Specifically, inadvertent DNA contamination or sample mixing would yield mosaic variation that could be erroneously interpreted as real mutation differences (instabilities) between tissues from the same individual. From the very beginning, mtDNA studies comparing cancerous to non-cancerous tissues have suffered from such mosaic results. We demonstrate here that the phylogenetic linkage of whole arrays of mtDNA mutations provides strong evidence of artificial recombination in previous studies on buccal cells and oral squamous cell carcinoma.gl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis work was partially supported by grants from the Xunta de Galicia (Grupos Emerxentes; 2008/037), Ministerio de Ciencia e Innovación (SAF2008-02971), and Fundación de Investigación Médica Mutua Madrileña (2008/CL444) given to ASgl
dc.identifier.citationBandelt, H., Salas, A. Contamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinoma. BMC Cancer 9, 113 (2009). https://doi.org/10.1186/1471-2407-9-113gl
dc.identifier.doi10.1186/1471-2407-9-113
dc.identifier.essn1471-2407
dc.identifier.urihttp://hdl.handle.net/10347/22769
dc.language.isoenggl
dc.publisherBMCgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/Plan Nacional de I+D+i 2008-2011/SAF2008-02971/ES/MITGENOMICS: UN PROYECTO PARA EL ANALISIS POBLACIONAL DE GENOMAS COMPLETOS MITOCONDRIALES. APLICACIONES FORENSES, MEDICAS Y ANTROPOLOGICAS
dc.relation.publisherversionhttps://doi.org/10.1186/1471-2407-9-113gl
dc.rights© 2009 Bandelt and Salas; licensee BioMed Central Ltd. 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 citedgl
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/2.0
dc.titleContamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinomagl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication2badffc8-442d-4308-ab23-2eafbb77f6ba
relation.isAuthorOfPublication.latestForDiscovery2badffc8-442d-4308-ab23-2eafbb77f6ba

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