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Multiple genotoxic activities of ptaquiloside in human lymphocytes: aneugenesis, clastogenesis and induction of sister chromatid exchange

dc.contributor.authorGil da Costa, R.M.
dc.contributor.authorCoelho, P.
dc.contributor.authorSousa, R.
dc.contributor.authorBastos, M.M.S.M.
dc.contributor.authorPorto, B.
dc.contributor.authorTeixeira, João Paulo
dc.contributor.authorMalheiro, I
dc.contributor.authorLopes, C.
dc.date.accessioned2013-02-08T15:19:49Z
dc.date.available2013-02-08T15:19:49Z
dc.date.issued2012-08-30
dc.description.abstractPtaquiloside, a norsesquiterpene glycoside from bracken (Pteridium aquilinum), is a known carcinogen towards animals. Its genotoxicity is mainly attributed to its DNA-alkylating and clastogenic properties. This study analyses various modes of genotoxic action of ptaquiloside in human mononuclear blood cells. The alkaline comet assay was performed on cells exposed to 5μg/ml ptaquiloside for 5, 10, 20, 30, 40 or 50min. Tail length was used as a DNA-damage parameter. Assays to determine structural and numerical chromosomal aberrations and sister-chromatid exchange were conducted on cells exposed to 5, 10 or 20μg/ml ptaquiloside for 48h. The tail length showed maximum DNA damage at 20-30min, diminishing onwards. Highly significant (p<0.001) dose-dependent increases in structural and numerical chromosomal aberrations and SCE were observed in response to ptaquiloside. These results indicate that ptaquiloside is not only a DNA-alkylating agent, but expresses its genotoxicity through multiple mechanisms including clastogenesis, aneugenesis and the mechanism underlying SCE induction, which is not entirely understood. Recent studies support the role played by aneuploidy in oncogenesis, highlighting the importance of this endpoint for mutagenicity screening. SCE are thought to represent the long-term effects of mutagens and are an important genotoxicity biomarker. The present results also agree with data from epidemiological studies and from animal in vivo studies, further supporting the hypothesis that ptaquiloside may represent a significant threat to human health.por
dc.identifier.citationMutat Res. 2012 Aug 30;747(1):77-81. Epub 2012 Apr 28por
dc.identifier.issn0027-5107
dc.identifier.otherdoi: 10.1016/j.mrgentox.2012.04.010
dc.identifier.urihttp://hdl.handle.net/10400.18/1203
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S1383571812001611por
dc.subjectBrackenpor
dc.subjectPtaquilosidepor
dc.subjectAneuploidypor
dc.subjectSCEpor
dc.subjectClastogenesispor
dc.subjectAr e Saúde Ocupacionalpor
dc.subjectGenotoxicidade Ambientalpor
dc.titleMultiple genotoxic activities of ptaquiloside in human lymphocytes: aneugenesis, clastogenesis and induction of sister chromatid exchangepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage81por
oaire.citation.startPage77por
oaire.citation.titleMutation Research - Fundamental and Molecular Mechanisms of Mutagenesispor
oaire.citation.volume747(1)por
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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