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Integration of cellular and molecular endpoints to assess the toxicity of polycyclic aromatic hydrocarbons in HepG2 cell line

dc.contributor.authorMorgado, Patrícia I.
dc.contributor.authorJose, Sílvia
dc.contributor.authorWanke, Riccardo
dc.contributor.authorAntunes, Alexandra M.M.
dc.contributor.authorSofia Cardoso, Ana
dc.contributor.authorJordao, Luisa
dc.date.accessioned2018-02-12T14:39:51Z
dc.date.available2018-09-09T00:30:11Z
dc.date.issued2017-12
dc.description.abstractPolycyclic aromatic hydrocarbons (PAHs) are persistent pollutants present in the environment with known mutagenic and carcinogenic properties. In the present study the effect of exposure to single or multiple doses of benzo[a]anthracene (BaA), pyrene (Pyr) and three halogenated derivatives of these compounds (1-ClPyr; 1-BrPyr and 7-ClBaA) were evaluated in a liver-derived human cell line (HepG2). Cytotoxicity as assessed by the classic MTT and neutral red assays showed a mild toxic effect in response to single or multiple dose exposure for up to 72h; except for multiple dose exposure to BaA and 7-ClBaA (1μM per day during 4 days) and single exposure to 10 μM BaA. Furthermore, selective mitochondrial and lysosomal toxicity was observed for Pyr and BaA series, respectively. In order to understand the underlying molecular mechanisms responsible for this effect ROS production, mitochondrial membrane depolarization, lysosomal pH, DNA fragmentation, early and late apoptosis mediators were evaluated after exposure to single doses of the compounds. All compounds were able to trigger oxidative stress after 24h as measured by catalase activity and a good correlation was found between mitochondrial membrane depolarization, lysosomal pH increase and MTT and neutral red assays, respectively. The evaluation of cell death mediators showed that caspase-3/7 but not annexin-V pathways were involved in toxicity triggered by the studied compounds. The integration of all results showed that 1-BrPyr and BaA have a higher toxicity potential.pt_PT
dc.description.sponsorshipThis work was supported by Fundação para a Ciência e a Tecnologia (FCT) [RECI/QEQ-MED/0330/2012] and Sílvia José work was supported by INSA [BRJ-DSA/2012].pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationEnviron Toxicol Chem. 2017 Dec;36(12):3404-3414. doi: 10.1002/etc.3927. Epub 2017 Sep 8.pt_PT
dc.identifier.doi10.1002/etc.3927pt_PT
dc.identifier.issn730-7268
dc.identifier.urihttp://hdl.handle.net/10400.18/4936
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherWileypt_PT
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/wol1/doi/10.1002/etc.3927/abstractpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt_PT
dc.subjectPolycyclic Aromatic Hydrocarbons (PAHs)pt_PT
dc.subjectCytotoxicitypt_PT
dc.subjectBioaccumulationpt_PT
dc.subjectOrganic Contaminantspt_PT
dc.subjectToxic Effectspt_PT
dc.subjectWater Disinfectionpt_PT
dc.subjectProgrammed Cell Deathpt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.titleIntegration of cellular and molecular endpoints to assess the toxicity of polycyclic aromatic hydrocarbons in HepG2 cell linept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/RECI%2FQEQ-MED%2F0330%2F2012/PT
oaire.citation.conferencePlaceHoboken, NJpt_PT
oaire.citation.endPage3414pt_PT
oaire.citation.issue12pt_PT
oaire.citation.startPage3404pt_PT
oaire.citation.titleEnvironmental Toxicology and Chemistrypt_PT
oaire.citation.volume36pt_PT
oaire.fundingStream3599-PPCDT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsembargoedAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublication46b679be-28f2-4c4b-a53e-e6b654bf46ce
relation.isProjectOfPublication.latestForDiscovery46b679be-28f2-4c4b-a53e-e6b654bf46ce

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