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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/12895
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dc.contributor.authorGrassi, Tony Fernando-
dc.contributor.authorRodrigues, Maria Aparecida Marchesan-
dc.contributor.authorCamargo, João Lauro Viana de-
dc.contributor.authorBarbisan, Luis Fernando-
dc.date.accessioned2014-05-20T13:37:19Z-
dc.date.accessioned2016-10-25T16:54:02Z-
dc.date.available2014-05-20T13:37:19Z-
dc.date.available2016-10-25T16:54:02Z-
dc.date.issued2011-04-01-
dc.identifierhttp://dx.doi.org/10.1177/0192623310396904-
dc.identifier.citationToxicologic Pathology. Thousand Oaks: Sage Publications Inc, v. 39, n. 3, p. 486-495, 2011.-
dc.identifier.issn0192-6233-
dc.identifier.urihttp://hdl.handle.net/11449/12895-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/12895-
dc.description.abstractThis study aimed to evaluate the carcinogenic potential of the herbicide Diuron in a two-stage rat medium-term mammary carcinogenesis model initiated by 7,12-dimethylbenz(a)anthracene (DMBA). Female seven-week-old Sprague-Dawley (SD) rats were allocated to six groups: groups G1 to G4 received intragastrically (i.g.) a single 50 mg/kg dose of DMBA; groups G5 and G6 received single administration of canola oil (vehicle of DMBA). Groups G1 and G5 received a basal diet, and groups G2, G3, G4, and G6 were fed the basal diet with the addition of Diuron at 250, 1250, 2500, and 2500 ppm, respectively. After twenty-five weeks, the animals were euthanized and mammary tumors were histologically confirmed and quantified. Tumor samples were also processed for immunohistochemical evaluation of the expressions of proliferating cell nuclear antigen (PCNA), cleaved caspase-3, estrogen receptor-alpha (ER-alpha), p63, bcl-2, and bak. Diuron treatment did not increase the incidence or multiplicity of mammary tumors (groups G2 to G4 versus Group G1). Also, exposure to Diuron did not alter tumor growth (cell proliferation and apoptosis indexes) or immunoreactivity to ER-alpha, p63 (myoephitelial marker), or bcl-2 and bak (apoptosis regulatory proteins). These findings indicate that Diuron does not have a promoting potential on mammary carcinogenesis in female SD rats initiated with DMBA.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipTOXICAM (Centre of the Evaluation of the Impact of the Environment on Human Health, Department of Pathology - Botucatu Medical School, UNESP, Brazil)-
dc.format.extent486-495-
dc.language.isoeng-
dc.publisherSage Publications Inc-
dc.sourceWeb of Science-
dc.subjectpesticidesen
dc.subjectdiuronen
dc.subjectmammary carcinogenesisen
dc.subjectSprague-Dawley ratsen
dc.subjecttoxicologyen
dc.titleEvaluation of Carcinogenic Potential of Diuron in a Rat Mammary Two-Stage Carcinogenesis Modelen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUNESP São Paulo State Univ, Inst Biosci, Dept Morphol, Botucatu, SP, Brazil-
dc.description.affiliationUNESP São Paulo State Univ, Dept Pathol, Sch Med, Botucatu, SP, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Inst Biosci, Dept Morphol, Botucatu, SP, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Dept Pathol, Sch Med, Botucatu, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 06/01330-0-
dc.identifier.doi10.1177/0192623310396904-
dc.identifier.wosWOS:000293380100004-
dc.rights.accessRightsAcesso aberto-
dc.relation.ispartofToxicologic Pathology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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