1. Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer
- Author
-
Mauro Zamboni, José Roberto Lapa e Silva, Amanda B. Moraes, Veronica Aran, Cinthya Sternberg, Joyce L. Moraes, Luciene Schluckbier, Emanuela de Moraes, Marcelo Ribeiro Alves, Edson Toscano, Carlos Gil Ferreira, and Mariana Lemos Duarte
- Subjects
0301 basic medicine ,Oncology ,Cancer Research ,medicine.medical_specialty ,Biology ,medicine.disease_cause ,polymorphism ,Metastasis ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,cyclooxygenase 2 ,Lung cancer ,Oncogene ,Retrospective cohort study ,Articles ,cohort ,medicine.disease ,Molecular medicine ,Reverse transcriptase ,lung cancer ,tumorigenesis ,030104 developmental biology ,Real-time polymerase chain reaction ,030220 oncology & carcinogenesis ,Cancer research ,Carcinogenesis - 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.
- Published
- 2017
- Full Text
- View/download PDF