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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/130245
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dc.contributor.authorFonseca-Alves, Carlos Eduardo-
dc.contributor.authorTiagua Vicente, Igor Simoes-
dc.contributor.authorRivera Calderon, Luis Gabriel-
dc.contributor.authorJusto, Andre Augusto-
dc.contributor.authorRogatto, Silvia Regina-
dc.contributor.authorLaufer-Amorim, Renee-
dc.date.accessioned2015-11-03T15:30:35Z-
dc.date.accessioned2016-10-25T21:18:48Z-
dc.date.available2015-11-03T15:30:35Z-
dc.date.available2016-10-25T21:18:48Z-
dc.date.issued2014-10-01-
dc.identifierhttp://cancerres.aacrjournals.org/content/74/19_Supplement/88-
dc.identifier.citationCancer Research. Philadelphia: Amer Assoc Cancer Research, v. 74, n. 19, 1 p., 2014.-
dc.identifier.issn0008-5472-
dc.identifier.urihttp://hdl.handle.net/11449/130245-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/130245-
dc.description.abstractBackground: The epithelial-mesenchymal transition (EMT) is an essential process in the tumor progression and metastasis. In human prostate carcinoma (PCa), the upregulation of cytokeratin and E-cadherin and down-regulation of vimentin have been associated with aggressive phenotype and poor prognosis. Due to the importance of canine cancer model it was evaluated the immunoexpression of AE1/AE3, E-cadherin and vimentin in canine prostatic lesions. Patients and Methods: A total of 75 prostatic tissues formalin-fixed paraffin embedded from dogs was selected: 10 normal prostatic tissues, 20 benign prostatic hyperplasia (BPH), 25 proliferative inflammatory atrophy (PIA) and 20 PCa. AE1/AE3 was detected with a monoclonal antibody (Invitrogen, 180132) at a 1:300 dilution, applied for 45 min at room temperature (RT). The antibody against Vimentin (V9, Invitrogen) and E-cadherin (NCH-38, Dako cytomatiomn) were monoclonal mouse antibodies, used at a 1:300 and 1:200, respectively, for 45 min at RT. The immunolabelling was performed by a polymer method (Histofine, Nichirei Biosciences,). A negative control was performed for all antibodies by omitting the primary antibody and substituting with Tris-buffered saline. The percentage of C-MYC, E-cadherin, and p63- positive cells per lesion was evaluated according to Prowatke et al. (2007). The samples were scored separately according to staining intensity and graded semi-quantitatively as negative, weakly positive, moderately positive, and strongly positive. The score was done in one 400 magnification field, considering only the lesion, since this was done in a TMA core of 1 mm. For statistical analyses, the immunostaining classifications were reduced to two categories: negative and positive. The negative category included negative and weakly positive staining. Chi-square or Fisher exact test was used to determine the association between the categorical variables. Results: All prostatic normal and BPH tissue were positive for cytokeratin, E-cadherin and negative for vimentin. Similarly, all PIA samples were positive for AE1/AE3. From those samples, 48% (12/25) were also positive for vimentin. 55% of PCa (11/25) was positive for vimentin and among these samples 75% (6/11) was also positive for AE1/AE3 and 45% (5/11) was negative for AE1/AE3. PIA and PCa presented a higher number of vimentin positive cells when compared with normal tissue (p=0.032). E-cadherin expression had no statistical difference among diagnosis groups, but we found a higher number of positive cases, with more than 51% of positive immunostaining in BPH and PIA (81.25% and 78.60% of the cases, respectively) than in PCa (55.55%). Conclusion: The carcinogenesis process regarding prostatic epithelial cells in dogs showed higher vimentin protein expression associated with concomitant loss of the cytokeratin and E-cadherin, similar in humans.en
dc.format.extent1-
dc.language.isoeng-
dc.publisherAmer Assoc Cancer Research-
dc.sourceWeb of Science-
dc.titleEpithelial-mesenchymal transition occurs in preneoplastic and neoplastic lesions of canine prostateen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationSao Paulo State Univ, Botucatu, SP, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Botucatu, SP, Brazil-
dc.identifier.doihttp://dx.doi.org/10.1158/1538-7445.AM2014-88-
dc.identifier.wosWOS:000349906900087-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofCancer Research-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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