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Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis
AIM OF THE STUDY: Results of recent published studies on the association between the COX-2 8473T>C polymorphism and the risk of breast cancer have often been conflicting. To make a more precise estimation of the potential relationship, a meta-analysis was performed. MATERIAL AND METHODS: A total...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269000/ https://www.ncbi.nlm.nih.gov/pubmed/25520577 http://dx.doi.org/10.5114/wo.2014.41394 |
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author | Jiang, Jun Quan, Xun-Feng Zhang, Li Shen, Li Zhang, Ming-Xia Ma, Hui-hui Wang, Yi-Chun |
author_facet | Jiang, Jun Quan, Xun-Feng Zhang, Li Shen, Li Zhang, Ming-Xia Ma, Hui-hui Wang, Yi-Chun |
author_sort | Jiang, Jun |
collection | PubMed |
description | AIM OF THE STUDY: Results of recent published studies on the association between the COX-2 8473T>C polymorphism and the risk of breast cancer have often been conflicting. To make a more precise estimation of the potential relationship, a meta-analysis was performed. MATERIAL AND METHODS: A total of seven case-control studies with 7,033 cases and 9,350 controls were included in the current meta-analysis through searching the databases of PubMed, Embase, and Cochrane Library (up to March 1(st), 2013). The odds ratio (OR) and 95% confidence interval (95% CI) were calculated to assess the strength of the association. The meta-analysis was conducted in a fixed/random effect model. RESULTS: We found no significant associations for all genetic models after all studies were pooled into the meta-analysis (for C vs. T: OR = 0.974, 95% CI: 0.906–1.047, p = 0.471; for CC vs. TT: OR = 0.957, 95% CI: 0.803–1.140, p = 0.62; for TC vs. TT: OR = 0.964, 95% CI: 0.881–1.055, p = 0.421; for CC + TC vs. TT: OR = 0.963, 95% CI: 0.880–1.053, p = 0.406; for CC vs. TT + TC: OR = 0.978, 95% CI: 0.831–1.15, p = 0.788). We also observed no obvious associations in the subgroup analyses by ethnicity (Caucasian) and source of controls (population based, PB) for all genetic models. CONCLUSIONS: Current evidence suggests that the COX-2 8473T>C polymorphism is not associated with breast cancer risk. |
format | Online Article Text |
id | pubmed-4269000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-42690002014-12-17 Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis Jiang, Jun Quan, Xun-Feng Zhang, Li Shen, Li Zhang, Ming-Xia Ma, Hui-hui Wang, Yi-Chun Contemp Oncol (Pozn) Original Paper AIM OF THE STUDY: Results of recent published studies on the association between the COX-2 8473T>C polymorphism and the risk of breast cancer have often been conflicting. To make a more precise estimation of the potential relationship, a meta-analysis was performed. MATERIAL AND METHODS: A total of seven case-control studies with 7,033 cases and 9,350 controls were included in the current meta-analysis through searching the databases of PubMed, Embase, and Cochrane Library (up to March 1(st), 2013). The odds ratio (OR) and 95% confidence interval (95% CI) were calculated to assess the strength of the association. The meta-analysis was conducted in a fixed/random effect model. RESULTS: We found no significant associations for all genetic models after all studies were pooled into the meta-analysis (for C vs. T: OR = 0.974, 95% CI: 0.906–1.047, p = 0.471; for CC vs. TT: OR = 0.957, 95% CI: 0.803–1.140, p = 0.62; for TC vs. TT: OR = 0.964, 95% CI: 0.881–1.055, p = 0.421; for CC + TC vs. TT: OR = 0.963, 95% CI: 0.880–1.053, p = 0.406; for CC vs. TT + TC: OR = 0.978, 95% CI: 0.831–1.15, p = 0.788). We also observed no obvious associations in the subgroup analyses by ethnicity (Caucasian) and source of controls (population based, PB) for all genetic models. CONCLUSIONS: Current evidence suggests that the COX-2 8473T>C polymorphism is not associated with breast cancer risk. Termedia Publishing House 2014-06-18 2014 /pmc/articles/PMC4269000/ /pubmed/25520577 http://dx.doi.org/10.5114/wo.2014.41394 Text en Copyright © 2014 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Jiang, Jun Quan, Xun-Feng Zhang, Li Shen, Li Zhang, Ming-Xia Ma, Hui-hui Wang, Yi-Chun Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis |
title | Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis |
title_full | Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis |
title_fullStr | Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis |
title_full_unstemmed | Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis |
title_short | Lack of association between COX-2 8473T>C polymorphism and breast cancer risk: a meta-analysis |
title_sort | lack of association between cox-2 8473t>c polymorphism and breast cancer risk: a meta-analysis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269000/ https://www.ncbi.nlm.nih.gov/pubmed/25520577 http://dx.doi.org/10.5114/wo.2014.41394 |
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