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Determining oxidative and non-oxidative genotoxic effects driven by estuarine sediment contaminants on a human hepatoma cell line

datacite.subject.sdg14:Proteger a Vida Marinha
dc.contributor.authorCosta, Pedro M.
dc.contributor.authorLouro, Henriqueta
dc.contributor.authorCosta, Maria Helena
dc.contributor.authorLavinha, João
dc.contributor.authorCaeiro, Sandra
dc.contributor.authorSilva, Maria João
dc.date.accessioned2015-03-02T10:56:00Z
dc.date.available2015-03-02T10:56:00Z
dc.date.issued2014-02
dc.description.abstractEstuarine sediments may be reservoirs of hydrophilic and hydrophobic pollutants, many of which are acknowl- edged genotoxicants, pro-mutagens and even potential carcinogens for humans. Still, studies aiming at narrowing the gap between ecological and human health risk of sediment-bound contaminant mixtures are scarce. Taking an impacted estuary as a case study (the Sado, SW Portugal), HepG2 (human hepatoma) cells were exposed in vitro for 48 h to extracts of sediments collected from two areas (urban/industrial and Triverine/agricultural), both contaminated by distinct mixtures of organic and inorganic toxicants, among which are found priority mutagens such as benzo[a]pyrene. Comparatively to a control test, extracts of sediments from both impacted areas produced deleterious effects in a dose–response manner. However, sediment extracts from the industrial area caused lower replication index plus higher cytotoxicity and genotoxicity (concerning total DNA strand breakage and clastogenesis), with emphasis on micronucleus induction. On the other hand, extracts from the rural area induced the highest oxidative damage to DNA, as revealed by the FPG (formamidopyrimidine-DNA glycosylase) enzyme in the Comet assay. Although the estuary, on its whole, has been classified as moderately contaminated, the results suggest that the sediments from the industrial area are significantly genotoxic and, furthermore, elicit permanent chromosome damage, thus potentially being more mutagenic than those from the rural area. The results are consistent with contamination by pro-mutagens like polycyclic aromatic hydrocarbons (PAHs), potentiated by metals. The sediments from the agriculture-influenced area likely owe their genotoxic effects to metals and other toxicants, probably pesticides and fertilizers, and able to induce reactive oxygen species without the formation of DNA strand breakage. The findings suggest that the mixtures of contaminants present in the assayed sediments are genotoxic to HepG2 cells, ultimately providing a useful approach to hazard identification and an effective line-of-evidence in the environmental monitoring of anthropogenically-impacted coastal ecosystems.por
dc.description.sponsorshipThe present research was financed by FCT and co-financed by the European Community FEDER through the program COMPETE (project reference PTDC/SAU-ESA/100107/2008). P.M. Costa was supported by the Portuguese Science and Technology Foundation (FCT) through the grant SFRH/BPD/72564/2010. The authors are thankful to A.R. Collins 34 M. Pinto et al. / Science of the Total Environment 478 (2014) 25–35 (University of Oslo, Norway) for supplying FPG and also acknowledge the contributions of J. Lobo, M. Martins and S. Carreira (IMAR).
dc.identifier.doihttp://dx.doi.org/10.1016/j.scitotenv.2014.01.084
dc.identifier.issn0048-9697
dc.identifier.urihttp://hdl.handle.net/10400.2/3734
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.subjectSediment contaminationpor
dc.subjectHepG2por
dc.subjectDNA damagepor
dc.subjectMicronucleipor
dc.subjectOxidative stresspor
dc.titleDetermining oxidative and non-oxidative genotoxic effects driven by estuarine sediment contaminants on a human hepatoma cell linepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage35por
oaire.citation.startPage25por
oaire.citation.titleScience of the Total Environmentpor
oaire.citation.volume478por
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
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublicatione2a8250a-8f09-4f11-a04e-1a3056644ff3
relation.isAuthorOfPublication.latestForDiscoverye2a8250a-8f09-4f11-a04e-1a3056644ff3

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