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2018-12-31
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- INI - Artigos de Periódicos [3522]
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FUNCTIONAL ANALYSIS OF POLYMORPHISMS IN THE COX-2 GENE AND RISK OF LUNG CANCER
Author
Affilliation
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Fundação Oswaldo cruz. Instituto Nacional de Infectologia Evandro Chagas. Rio de Janeiro, RJ, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Departamento de Cirurgia Torácica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Departamento de Cirurgia Torácica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Universidade Federal do Rio de Janeiro. Hospital Universitário Clementino Fraga Filho. Instituto de Medicina Torácica. Rio de Janeiro, RJ, Brasil.
National Clinical Cancer Research Network (RNPCC) SCTIE/MS. / Instituto D'Or de Pesquisa e Ensino, Rio de Janeiro, Brazil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Fundação Oswaldo cruz. Instituto Nacional de Infectologia Evandro Chagas. Rio de Janeiro, RJ, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Departamento de Cirurgia Torácica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Departamento de Cirurgia Torácica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Instituto Nacional de Câncer José Alencar Gomes da Silva, Divisão de Pesquisa Clínica, Rio de Janeiro, Rj, Brasil
Universidade Federal do Rio de Janeiro. Hospital Universitário Clementino Fraga Filho. Instituto de Medicina Torácica. Rio de Janeiro, RJ, Brasil.
National Clinical Cancer Research Network (RNPCC) SCTIE/MS. / Instituto D'Or de Pesquisa e Ensino, Rio de Janeiro, Brazil
Abstract
The enzyme cyclooxygenase 2 (COX-2) is known to be involved in tumorigenesis and metastasis in certain types of cancer. Nevertheless, the prognostic value of COX-2 overexpression and its polymorphisms in patients with non-small cell lung cancer (NSCLC) have yet to be fully elucidated. The aim of the present study was to investigate the association between the three most commonly studied COX-2 gene polymorphisms (-1195 G/A, -765 G/C and 8473 T/C) with COX-2 expression and lung cancer risk in a Brazilian cohort. In the present hospital based, case-control retrospective study, 104 patients with NSCLC and 202 cancer free control subjects were genotyped for -1195 G/A, -765 G/C and 8473 T/C polymorphisms using allelic discrimination with a reverse transcription quantitative polymerase chain reaction method. COX-2 mRNA expression was analyzed in surgically resected tumors from 34 patients with NSCLC. The results revealed that COX-2 expression levels were higher in tumor tissue compared with normal lung tissue. However, this overexpression of COX-2 was not associated with the patient outcome, and furthermore, none of the analyzed polymorphisms were associated with the risk of developing lung cancer, COX-2 overexpression, or the overall survival of the patients with NSCLC. Taken together, the findings described in the present study do not support a major role for COX-2 polymorphisms and COX-2 overexpression in lung carcinogenesis within the Brazilian population.
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