Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/26650
Title: Immunohistochemical detection of p53 protein expression as a prognostic indicator in Wilms tumor
Authors: Sredni, S. T.
Camargo, B. de
Lopes, L. F.
Teixeira, R.
Simpson, A.
Universidade Federal de São Paulo (UNIFESP)
Hosp Canc
Ludwig Inst Canc Res
Keywords: Wilms tumors
pathology
anaplasia
p53
prognosis
Issue Date: 1-Nov-2001
Publisher: Wiley-Blackwell
Citation: Medical and Pediatric Oncology. New York: Wiley-liss, v. 37, n. 5, p. 455-458, 2001.
Abstract: Background. Mutations of the tumor suppressor gene p53 are commonly found in several kinds of human cancer. in some types of neoplasms, accumulation of p53 protein has been reported to correlate with more aggressive clinical behavior. the role of p53 expression in Wilms tumors (WT) is not clear yet, but most studies have confirmed its correlation with anaplasia and advanced stage disease. Procedure. Ninety-seven WT were evaluated for p53 expression by immunohistochemistry in formalin-fixed parafin-embedded tissue and correlated with outcome. Tumors were classified as p53-Negative (p53-N) when no positivity was observed or only few cells showed weak positivity (0/1+) and p53-Positive (p53-P) when there was a diffuse and strong nuclear positivity (2+/3). Results. p53-P was detected in 13 out of 97 tumors and was associated with disease relapse (39 vs .17%; P = 0.06) but not with anaplasia. Among p53-N patients only 5% had metastatic disease compared with 31% of the p53-P sample. (P = 0.038). Overall survival was 94% for patients with p53-N vs. 85% for patients with p53-P at 1 year (P = 0.34). Conclusions. p53 expression in Wilms tumor detected by immunohistochemistry seems to be associated with advanced disease and relapse. (C) 2001 Wiley-Liss, Inc.
URI: http://repositorio.unifesp.br/handle/11600/26650
ISSN: 0098-1532
Other Identifiers: http://dx.doi.org/10.1002/mpo.1229
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.