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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Overexpression of Vimentin in Canine Prostatic Carcinoma

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Autor(es):
Rodrigues, M. M. P. [1] ; Rema, A. [2] ; Gaertner, F. [3, 2] ; Soares, F. A. [4] ; Rogatto, S. R. [5] ; De Mour, V. M. B. D. [6] ; Laufer-Amorim, R. [1]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] Sao Paulo State Univ UNESP, Dept Clin Vet Med, Botucatu, SP - Brazil
[2] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Oporto - Portugal
[3] Univ Porto IPATIMUP, Inst Mol Pathol & Immunol, Oporto - Portugal
[4] AC Camargo Hosp, Dept Pathol, Sao Paulo - Brazil
[5] Sao Paulo State Univ UNESP, Dept Urol, Botucatu, SP - Brazil
[6] Univ Fed Goias, Sch Vet Med, Goiania, Go - Brazil
Número total de Afiliações: 6
Tipo de documento: Artigo Científico
Fonte: Journal of Comparative Pathology; v. 144, n. 4, p. 308-311, MAY 2011.
Citações Web of Science: 4
Resumo

Canine prostatic tumours exhibit similarities to those of man and may represent a useful model system to explore the mechanisms of cancer progression. Tumour progression to malignancy requires a change from an epithelial phenotype to a fibroblastic or mesenchymal phenotype. Vimentin expression is associated with the invasive phenotype of human prostate cancer cells. The aim of the present study was to characterize immunohistochemically the expression of vimentin by canine prostatic carcinomas. Primary carcinomas and metastatic tumour foci both showed vimentin expression. This finding suggests that the acquisition of the epithelial-mesenchymal transition phenotype in canine prostatic carcinoma may be characterized by the presence of mesenchymal intermediate filament (vimentin) that could lead to a higher likelihood of metastasis. Published by Elsevier Ltd. (AU)

Processo FAPESP: 06/61814-1 - Atipia do epitélio prostático canino: aspectos moleculares e imunofenotípicos
Beneficiário:Renee Laufer Amorim
Modalidade de apoio: Auxílio à Pesquisa - Regular