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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/18618
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dc.contributor.authorGoncalves, Bianca F.-
dc.contributor.authorZanetoni, Cristiani-
dc.contributor.authorScarano, Wellerson R.-
dc.contributor.authorGoes, Rejane M.-
dc.contributor.authorVilamaior, Patricia S. L.-
dc.contributor.authorTaboga, Sebastiao R.-
dc.contributor.authorCampos, Silvana G. P.-
dc.date.accessioned2014-05-20T13:52:06Z-
dc.date.accessioned2016-10-25T17:03:17Z-
dc.date.available2014-05-20T13:52:06Z-
dc.date.available2016-10-25T17:03:17Z-
dc.date.issued2010-02-01-
dc.identifierhttp://dx.doi.org/10.1016/j.yexmp.2009.09.017-
dc.identifier.citationExperimental and Molecular Pathology. San Diego: Academic Press Inc. Elsevier B.V., v. 88, n. 1, p. 96-106, 2010.-
dc.identifier.issn0014-4800-
dc.identifier.urihttp://hdl.handle.net/11449/18618-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/18618-
dc.description.abstractIn the present study prostate lesions were induced in gerbils (Meriones unguiculatus) treated with a single N-methyl-N-nitrosourea (MNU) dose; thus, the incidence, latency and histology of these lesions were evaluated. Fibrillar elements of the extracellular matrix associated with microinvasive sites were also investigated. Animals were divided into 5 groups, including 2 control groups: (1) remained untreated; (2) received the corn oil vehicle (vehicle, 0.1 ml/application) and three different tumor induction regimens: (1) received MNU (30 mg/kg) and weekly testosterone (2 mg/kg) (MNU + testosterone); (2) received only MNU (30 mg/kg); (3) received weekly testosterone doses (2 mg/kg). After 3 and 6 months the animals were dissected and the prostates were evaluated morphologically, immunohistochemically and quantitatively. MNU plus androgen contributed to the development of prostatic intraepithelial neoplasia, microinvasive carcinoma and adenocarcinoma in gerbil prostate. However, these lesions occurred earlier in time in groups that received MNU and androgen compared to control animals as they over time also developed to a high extent microinvasive lesions. Cytochemistry and immunohistochemistry showed that these injuries were commonly associated with inflammatory cells whereas the epithelial cells presented proliferative activity. The alpha-methylacyl-CoA racemase (AMACR) expression in prostate cancer cells facilitated diagnosis of gerbil lesions. Testosterone, MNU and MNU + testosterone showed an increased epithelial volume, although the secretory activity was significantly suppressed mainly at neoplastic foci. In the prostatic stroma, reticular fibers increased significantly in MNU, MNU + testosterone and among the lesions found in these groups, while collagen fibers decreased at neoplastic sites. The disruption of the basement membrane was proven at malignant sites by ultrastructural analysis and type IV collagen and laminin degradation. The prostate carcinogenesis mediated by MNU and androgen stimulated the emergence of proliferative lesions in gerbils after short periods and showed the importance of a dynamic remodeling of stromal components for cellular invasiveness. Published by Elsevier B.V.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent96-106-
dc.language.isoeng-
dc.publisherAcademic Press Inc. Elsevier B.V.-
dc.sourceWeb of Science-
dc.subjectMNUen
dc.subjectTestosteroneen
dc.subjectProstate canceren
dc.subjectalpha-Methylacyl-CoA racemaseen
dc.subjectExtracellular matrixen
dc.subjectGerbilen
dc.titleProstate carcinogenesis induced by N-methyl-N-nitrosourea (mnu) in gerbils: Histopathological diagnosis and potential invasiveness mediated by extracellular matrix componentsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.description.affiliationSão Paulo State Univ, Inst Biosci Humanities & Exact Sci, UNESP IIBILCE, Dept Biol,Lab Microscopy & Microanal, BR-15054000 Sao Jose do Rio Preto, SP, Brazil-
dc.description.affiliationUniv Estadual Campinas, UNICAMP, Dept Cell Biol, Inst Biol, BR-13083864 Campinas, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, Dept Morphol, Inst Biosci, BR-18618000 Botucatu, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Inst Biosci Humanities & Exact Sci, UNESP IIBILCE, Dept Biol,Lab Microscopy & Microanal, BR-15054000 Sao Jose do Rio Preto, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Dept Morphol, Inst Biosci, BR-18618000 Botucatu, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 07/00467-5-
dc.description.sponsorshipIdFAPESP: 05/04670-4-
dc.description.sponsorshipIdCNPq: 301111/05-7-
dc.identifier.doi10.1016/j.yexmp.2009.09.017-
dc.identifier.wosWOS:000274500100014-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofExperimental and Molecular Pathology-
dc.identifier.orcid0000-0002-0970-4288pt
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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