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Prognostic value of E-cadherin, beta-catenin, MMPs (7 and 9), and TIMPs (1 and 2) in patients with colorectal carcinoma

2006; Wiley; Volume: 93; Issue: 2 Linguagem: Inglês

10.1002/jso.20413

1096-9098

Fernanda Roca, Laura V. Mauro, Ana Morandi, Fernando Bonadeo, Carlos Vaccaro, Guillermo Ojea Quintana, Sergio Specterman, Elisa Bal de Kier Joffé, Marı́a Guadalupe Pallotta, Lydia Puricelli, José Lastiri,

Cancer-related gene regulation

Background and Objectives Therapy of colorectal tumors (CRC) based on histology and clinical factors is insufficient to predict the evolution of each patient. The finding of molecular abnormalities able to differentiate subgroups of patients with bad prognosis will improve our ability to treat them successfully. Our purpose was to analyze retrospectively the prognostic input of E-cadherin, β-catenin, metalloproteinases (MMPs) (7 and 9), and tissue inhibitors of metalloproteinases (TIMPs) (1 and 2) in patients with a follow-up period of 5 years. Methods Antigen expression was analyzed by immunohistochemistry. Prognostic evaluation was performed with the multivariate proportional hazards model. Results We demonstrated a concomitant loss of E-cadherin and β-catenin at membranous level and an abnormal accumulation of nuclear β-catenin. Besides, we found that all MMPs and TIMPs studied were overexpressed in CRC tissue. There was no association between the expression of any of these molecules and the known clinical-pathological parameters employed in CRC pathology. A multivariate analysis demonstrated that the overall survival could be independently predicted by the loss of E-cadherin and the overexpression of TIMP-2. Conclusions The expression of E-cadherin and TIMP-2 could be relevant in determining the prognosis of CRC patients and providing a more accurate mechanism for their classification. J. Surg. Oncol. 2006;93: 151–160. © 2006 Wiley-Liss, Inc.