Publicação:
Antigenotoxicity and antimutagenicity of lycopene in HepG2 cell line evaluated by the comet assay and micronucleus test

dc.contributor.authorScolastici, C. [UNESP]
dc.contributor.authorde Lima, R. O. Alves [UNESP]
dc.contributor.authorBarbisan, Luis Fernando [UNESP]
dc.contributor.authorFerreira, Ana Lúcia dos Anjos [UNESP]
dc.contributor.authorRibeiro, D. A.
dc.contributor.authorSalvadori, Daisy Maria Favero [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T13:33:19Z
dc.date.available2014-05-20T13:33:19Z
dc.date.issued2008-03-01
dc.description.abstractEpidemiological studies have provided evidence that high consumption of tomatoes effectively reduces the risk of reactive oxygen species (ROS)-mediated diseases such as cancer. Tomatoes are rich sources of lycopene, a potent singlet oxygen-quenching carotenoid. In addition to its antioxidant properties, lycopene shows an array of biological effects including antimutagenic and anticarcinogenic activities. In the present study, the chemopreventive action of lycopene was examined on DNA damage and clastogenic or aneugenic effects of H2O2 and n-nitrosodiethylamine (DEN) in the metabolically competent human hepatoma cell line (HepG2 cells). Lycopene at concentrations of 10. 25, and 50 mu M, was tested under three protocols: before, simultaneously, and after treatment with the mutagen, using the comet and micronucleus assays. Lycopene significantly reduced the genotoxicity and mutagenicity of H2O2 in all of the conditions tested. For DEN, significant reductions of primary DNA damage (comet assay) were detected when the carotenoid (all of the doses) was added in the cell culture medium before or simultaneously with the mutagen. In the micronucleus test, the protective effect of lycopene was observed only when added prior to DEN treatment. In conclusion, our results suggest that lycopene is a suitable agent for preventing chemically-induced DNA and chromosome damage. (C) 2007 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUniv São Paulo, UNESP, Botucatu Med Sch, Dept Pathol, BR-05508 São Paulo, Brazil
dc.description.affiliationUniv São Paulo, UNESP, Inst Biosci, Botucatu, SP, Brazil
dc.description.affiliationUniv São Paulo, UNESP, Botucatu Med Sch, Dept Clin Med, BR-05508 São Paulo, Brazil
dc.description.affiliationUniv Fed São Paulo, UNIFESP, Dept Hlth Sci, Botucatu, SP, Brazil
dc.description.affiliationUnespUniv São Paulo, UNESP, Botucatu Med Sch, Dept Pathol, BR-05508 São Paulo, Brazil
dc.description.affiliationUnespUniv São Paulo, UNESP, Inst Biosci, Botucatu, SP, Brazil
dc.description.affiliationUnespUniv São Paulo, UNESP, Botucatu Med Sch, Dept Clin Med, BR-05508 São Paulo, Brazil
dc.format.extent510-514
dc.identifierhttp://dx.doi.org/10.1016/j.tiv.2007.11.002
dc.identifier.citationToxicology In Vitro. Oxford: Pergamon-Elsevier B.V. Ltd, v. 22, n. 2, p. 510-514, 2008.
dc.identifier.doi10.1016/j.tiv.2007.11.002
dc.identifier.issn0887-2333
dc.identifier.lattes2940051650846541
dc.identifier.lattes5051118752980903
dc.identifier.lattes3278528112652257
dc.identifier.urihttp://hdl.handle.net/11449/11394
dc.identifier.wosWOS:000254694500026
dc.language.isoeng
dc.publisherPergamon-Elsevier B.V. Ltd
dc.relation.ispartofToxicology in Vitro
dc.relation.ispartofjcr3.105
dc.relation.ispartofsjr0,931
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectlycopeneen
dc.subjectDNA damageen
dc.subjectantigenotoxicityen
dc.subjectantimutagenicityen
dc.subjectHepG2 cellsen
dc.titleAntigenotoxicity and antimutagenicity of lycopene in HepG2 cell line evaluated by the comet assay and micronucleus testen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderPergamon-Elsevier B.V. Ltd
dspace.entity.typePublication
unesp.author.lattes2940051650846541[4]
unesp.author.lattes5051118752980903
unesp.author.lattes3278528112652257[3]
unesp.author.orcid0000-0001-9323-3134[6]
unesp.author.orcid0000-0002-5267-1127[4]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt
unesp.departmentPatologia - FMBpt

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