Claudin expression is dysregulated in prostate adenocarcinomas but does not correlate with main clinicopathological parameters


Autoria(s): COUTINHO-CAMILLO, Claudia Malheiros; LOURENCO, Silvia Vanessa; FONSECA, Francisco Paulo da; SOARES, Fernando Augusto
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

Aims: Claudins, a large family of essential tight junction (TJ) proteins, are abnormally regulated in human carcinomas. The aim of this study was to determine the expression of claudins 1, 2, 3, 4, 5, 7, and 11 in prostate samples from Brazilian patients and correlate it with the clinicopathological features of prostate cancer. Methods: Using a tissue microarray (TMA) of specimens of prostate adenocarcinoma and benign prostatic hyperplasia (BPH) we analysed the expression of claudins 1, 2, 3, 4, 5, 7, and 11 by immunohistochemistry. Results: Claudin 4 was down-regulated and claudins 2, 3, and 5 were overexpressed in prostate adenocarcinomas compared with BPH samples. Expression of claudins 1 and 7 was similar in tumours and BPH samples. Claudin 11 was absent from all prostate samples. Overexpression of claudin 3 was associated with perineural invasion (p = 0.014) and tended to occur in advanced stages of the disease (p = 0.064). Increased expression of claudin 5 was marginally associated with perineural invasion (p = 0.060). Conclusions: Our results suggest that alterations in claudin expression occur in prostate cancer cells, although we have not found an association with the main clinicopathological parameters.

FAPESP[98/14335-2]

Identificador

PATHOLOGY, v.43, n.2, p.143-148, 2011

0031-3025

http://producao.usp.br/handle/BDPI/25668

10.1097/PAT.0b013e3283428099

http://dx.doi.org/10.1097/PAT.0b013e3283428099

Idioma(s)

eng

Publicador

LIPPINCOTT WILLIAMS & WILKINS

Relação

Pathology

Direitos

closedAccess

Copyright LIPPINCOTT WILLIAMS & WILKINS

Palavras-Chave #Claudins #immunohistochemistry #prostate cancer #tissue microarray #TIGHT JUNCTION PROTEINS #HUMAN COLORECTAL-CANCER #PANCREATIC-CANCER #BREAST #INVASION #THERAPY #TARGETS #LESIONS #BENIGN #GRADE #Pathology
Tipo

article

original article

publishedVersion