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The use of comet assay to assess global DNA methylation in human biomonitoring studies

dc.contributor.authorCosta, Carla
dc.contributor.authorAlves, Ana Catarina
dc.contributor.authorCosta, Solange
dc.contributor.authorSoares, Amadeu M.V.M.
dc.contributor.authorMonteiro, Marta S.
dc.contributor.authorLoureiro, Susana
dc.contributor.authorTeixeira, João Paulo
dc.date.accessioned2016-02-17T12:23:26Z
dc.date.available2016-02-17T12:23:26Z
dc.date.issued2015-09
dc.description.abstractThe Comet assay is a valuable tool for the detection of DNA damage in genotoxicity and human biomonitoring studies. Throughout the years, this biomarker has undergone several adaptations in their protocol in order to increase its sensitivity and the possible outcomes. By including an additional step of DNA digestion with lesion-specific endonucleases, the comet assay can provide information regarding the type of DNA damage detected in cells. The use of these enzymes has also allowed the development of a methylation-sensitive modified version of the comet assay. This version enables the routine measurement of global methylation, as well as CpG island DNA methylation in a variety of cells while simultaneously determining the genetic integrity of examined cells (Wentzel, 2012). Briefly, it makes use of isochizomeric restriction enzymes HpaII and MspI (that display differential sensitivity to DNA methylation) to characterize methylation outside CpG islands and restriction enzyme NotI to determine DNA methylation in CpG islands. The technique has been recently adapted to a medium-throughput version (Lewies, 2014) that allows the simultaneous analysis of a larger number of samples and overcomes some technical problems. Nevertheless, this technique has not yet been carried out in human biomonitoring studies. In this context, the aim of this work was to make use of this version of the comet assay to characterize global DNA methylation in approximately 50 human samples. Samples were analysed by the methylation-sensitive modified version of the comet assay (medium-throughput) and by ELISA based assay. Data obtained with both methods were compared and reproducibility of the methylation-sensitive modified version of the comet assay determined. Results obtained contribute to knowledge on the feasibility of this version of the comet assay and its possible usage in human biomonitoring studies as an epigenetic biomarker.pt_PT
dc.description.sponsorshipThis work was supported by The Portuguese Science Foundation (FCT) through CESAM (UID/AMB/50017/2013) and CNRS/INEE - National Center for Scientific Research/Institute of Ecology and Environment, via OHMI – International Observatory Hommes-Millieux. Carla Costa and Marta S. Monteiro are supported by the grants SFRH/BPD/96196/2013 and SFRH/BPD/45911/2008, respectively, funded by FCT (QREN – POPH – Type 4.1 – Advanced training, subsidized by the European Social Fund and national funds of MEC).pt_PT
dc.identifier.citationFront. Genet. Conference Abstract: ICAW 2015 - 11th International Comet Assay Workshop. doi: 10.3389/conf.fgene.2015.01.00015pt_PT
dc.identifier.doi10.3389/conf.fgene.2015.01.00015pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/3359
dc.language.isoengpt_PT
dc.relation.publisherversionhttp://www.frontiersin.org/10.3389/conf.fgene.2015.01.00015/event_abstractpt_PT
dc.subjectComet Assaypt_PT
dc.subjectDNA Methylationpt_PT
dc.subjectHuman Biomonitoringpt_PT
dc.subjectELISA Testpt_PT
dc.subjectHuman Cellspt_PT
dc.subjectGenotoxicitypt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.subjectAvaliação do Risco
dc.subjectAr e Saúde Ocupacional
dc.titleThe use of comet assay to assess global DNA methylation in human biomonitoring studiespt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FAMB%2F50017%2F2013/PT
oaire.citation.conferencePlaceAntuérpia, Bélgicapt_PT
oaire.citation.titleICAW 2015 - 11th International Comet Assay Workshop, 1-4 September 2015pt_PT
oaire.fundingStream5876
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isProjectOfPublication1d7db62a-6440-4ccb-a5cc-c3f76c8585b3
relation.isProjectOfPublication.latestForDiscovery1d7db62a-6440-4ccb-a5cc-c3f76c8585b3

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