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Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer

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...

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Autores principales: Moraes, Joyce L., Moraes, Amanda B., Aran, Veronica, Alves, Marcelo R., Schluckbier, Luciene, Duarte, Mariana, Toscano, Edson, Zamboni, Mauro, Sternberg, Cinthya, de Moraes, Emanuela, Lapa E Silva, José R., Ferreira, Carlos Gil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374939/
https://www.ncbi.nlm.nih.gov/pubmed/28413655
http://dx.doi.org/10.3892/mco.2017.1167
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author Moraes, Joyce L.
Moraes, Amanda B.
Aran, Veronica
Alves, Marcelo R.
Schluckbier, Luciene
Duarte, Mariana
Toscano, Edson
Zamboni, Mauro
Sternberg, Cinthya
de Moraes, Emanuela
Lapa E Silva, José R.
Ferreira, Carlos Gil
author_facet Moraes, Joyce L.
Moraes, Amanda B.
Aran, Veronica
Alves, Marcelo R.
Schluckbier, Luciene
Duarte, Mariana
Toscano, Edson
Zamboni, Mauro
Sternberg, Cinthya
de Moraes, Emanuela
Lapa E Silva, José R.
Ferreira, Carlos Gil
author_sort Moraes, Joyce L.
collection PubMed
description 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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spelling pubmed-53749392017-04-15 Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer Moraes, Joyce L. Moraes, Amanda B. Aran, Veronica Alves, Marcelo R. Schluckbier, Luciene Duarte, Mariana Toscano, Edson Zamboni, Mauro Sternberg, Cinthya de Moraes, Emanuela Lapa E Silva, José R. Ferreira, Carlos Gil Mol Clin Oncol Articles 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. D.A. Spandidos 2017-04 2017-02-16 /pmc/articles/PMC5374939/ /pubmed/28413655 http://dx.doi.org/10.3892/mco.2017.1167 Text en Copyright: © Moraes et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Moraes, Joyce L.
Moraes, Amanda B.
Aran, Veronica
Alves, Marcelo R.
Schluckbier, Luciene
Duarte, Mariana
Toscano, Edson
Zamboni, Mauro
Sternberg, Cinthya
de Moraes, Emanuela
Lapa E Silva, José R.
Ferreira, Carlos Gil
Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer
title Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer
title_full Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer
title_fullStr Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer
title_full_unstemmed Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer
title_short Functional analysis of polymorphisms in the COX-2 gene and risk of lung cancer
title_sort functional analysis of polymorphisms in the cox-2 gene and risk of lung cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374939/
https://www.ncbi.nlm.nih.gov/pubmed/28413655
http://dx.doi.org/10.3892/mco.2017.1167
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