MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality
- ANTÔNIO TALVANE TORRES DE OLIVEIRA1,
- DELCIO MATOS2,
- ANGELA FLÁVIA LOGULLO3,
- SANDRA REGINA MORINI DA SILVA4,
- RICARDO ARTIGIANI NETO3,
- ADHEMAR LONGATTO FILHO4,5 and
- SARHAN SYDNEY SAAD2
- 1Departments of Surgery and Pathology of Barretos Cancer Hospital, Pio XII Foundantion, Barretos, São Paulo
- 2Department of Gastroenterology, School of Medicine, Federal University of São Paulo, São Paulo, Brazil
- 3Department of Pathology, School of Medicine, Federal University of São Paulo, São Paulo, Brazil
- 4Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga, Portugal
- 5Laboratory of Medical Investigation (LIM) 14, Department of Pathology, University of São Paulo School of Medicine, São Paulo, Brazil
- Correspondence to: Antônio Talvane Torres de Oliveira, Rua Antenor Duarte Vilella, 1331, Bairro Dr. Paulo Prata, CEP 14784-400, Hospital de Câncer de Barretos, Fundação Pio XII, Barretos, SP, Brazil. e-mail: netto123{at}uol.com.br
Abstract
The aim of the present study was to evaluate by immunohistochemistry the prognostic meaning of the tumor marker MET (hepatocyte growth factor) in patients submitted to surgical resection due to primary colorectal adenocarcinoma. Patients and Methods: A retrospective study was carried out that included 286 consecutive patients with colorectal adenocarcinoma, submitted to surgical resection at Barretos Cancer Hospital, from 1993 to 2002. The histopathological expression of the MET tumor marker was evaluated using an anti-protein monoclonal antibody against MET by the streptavidin-biotin-peroxidase technique. The expression of the tumor marker was semi-quantitative, and the slide samples were independently analyzed by three pathologists unaware of patient clinical and histopathological data. Results: The tumor marker expression was positive in 236 (79%) out of a total of 286 patients. This expression was statistically significantly different between stages I and IV (p=0.004), for overall survival (p=0.009), and for cancer-related mortality rates (p=0.022). However, no association between the tumor marker and recurrence (p=0.89) or disease-free interval (p=0.91) was observed. Conclusion: MET has shown significant expression at advanced stages of the disease, as well as for overall survival and cancer-related mortality rates demonstrating to be a valuable marker for poor prognosis in colorectal cancer patients.
- Received June 4, 2009.
- Revision received September 14, 2009.
- Accepted September 22, 2009.
- Copyright© 2009 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved







