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An integrative assessment to determine the genotoxic hazard of estuarine sediments: combining cell and whole-organism responses

datacite.subject.sdg13:Ação Climática
dc.contributor.authorCosta, Pedro M.
dc.contributor.authorPinto, Miguel
dc.contributor.authorVicente, Ana
dc.contributor.authorGonçalves, Cátia
dc.contributor.authorRodrigo, Ana
dc.contributor.authorLouro, Henriqueta
dc.contributor.authorCosta, Maria Helena
dc.contributor.authorCaeiro, Sandra
dc.contributor.authorSilva, Maria João
dc.date.accessioned2015-03-02T11:26:26Z
dc.date.available2015-03-02T11:26:26Z
dc.date.issued2014-12
dc.description.abstractThe application of the Comet assay in environmental monitoring remains challenging in face of the complexity of environmental stressors, e.g., when dealing with estuarine sediments, that hampers the drawing of cause-effect relationships. Although the in vitro Comet assay may circumvent confounding factors, its application in environmental risk assessment (ERA) still needs validation. As such, the present work aims at integrating genotoxicity and oxidative DNA damage induced by sediment-bound toxicants in HepG2 cells with oxidative stress-related effects observed in three species collected from an impacted estuary. Distinct patterns were observed in cells exposed to crude mixtures of sediment contaminants from the urban/industrial area comparatively to the ones from the rural/riverine area of the estuary, with respect to oxidative DNA damage and oxidative DNA damage. The extracts obtained with the most polar solvent and the crude extracts caused the most significant oxidative DNA damage in HepG2 cells, as measured by the formamidopyrimidine-DNA glycosylase (FPG)-modified Comet assay. This observation suggests that metals and unknown toxicants more hydrophilic than polycyclic aromatic hydrocarbons may be important causative agents, especially in samples from the rural part of the estuary, where oxidative DNA damage was the most significant. Clams, sole, and cuttlefish responded differentially to environmental agents triggering oxidative stress, albeit yielding results accordant with the oxidative DNA damage observed in HepG2 cells. Overall, the integration of in vivo biomarker responses and Comet assay data in HepG2 cells yielded a comparable pattern, indicating that the in vitro FPG-modified Comet assay may be an effective and complementary line-of-evidence in ERA even in particularly challenging, natural, scenarios such as estuarine environments.por
dc.identifier.citationCosta, Pedro M. [et al.] - An integrative assessment to determine the genotoxic hazard of estuarine sediments : combining cell and whole-organism responses. "Frontiers in Genetics" [Em linha]. ISSN 1664-8021 (Print) ISSN 1664-8021 (Online). Vol. 5 (dez. 2014), 12 p.
dc.identifier.doi10.3389/fgene.2014.00437
dc.identifier.issn1664-8021
dc.identifier.issn1664-8021
dc.identifier.urihttp://hdl.handle.net/10400.2/3737
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherFrontierspor
dc.subjectComet assaypor
dc.subjectEnvironmental risk assessmentpor
dc.subjectSediment contaminationpor
dc.subjectOxidative stresspor
dc.subjectHepG2 cellspor
dc.titleAn integrative assessment to determine the genotoxic hazard of estuarine sediments: combining cell and whole-organism responsespor
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/PTDC%2FSAU-ESA%2F100107%2F2008/PT
oaire.citation.endPage12por
oaire.citation.startPage1por
oaire.citation.titleFrontiers in Geneticspor
oaire.citation.volume5(437)por
oaire.fundingStream5876-PPCDTI
person.familyNameCaeiro
person.givenNameSandra
person.identifier587808
person.identifier.ciencia-id8515-398A-D241
person.identifier.orcid 0000-0002-6079-3554
person.identifier.ridK-3886-2014
person.identifier.scopus-author-id6603297853
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicatione2a8250a-8f09-4f11-a04e-1a3056644ff3
relation.isAuthorOfPublication.latestForDiscoverye2a8250a-8f09-4f11-a04e-1a3056644ff3
relation.isProjectOfPublication551ec92b-366a-4b5d-8de9-21f8d6067454
relation.isProjectOfPublication.latestForDiscovery551ec92b-366a-4b5d-8de9-21f8d6067454

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