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Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk
BACKGROUND: Molecular epidemiological studies have demonstrated a closer association between Fas/FasL polymorphisms and head and neck cancer (HNC) risk, and the results of these published studies were inconsistent. We therefore performed this meta-analysis to explore the associations between Fas/Fas...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944675/ https://www.ncbi.nlm.nih.gov/pubmed/29419701 http://dx.doi.org/10.1097/MD.0000000000009873 |
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author | Zhang, Dan-Feng Jiang, Guang-Bin Qin, Chuan-Qi Liu, De-Xi Hu, Ya-Jun Zhou, Juan Niu, Yu-Ming |
author_facet | Zhang, Dan-Feng Jiang, Guang-Bin Qin, Chuan-Qi Liu, De-Xi Hu, Ya-Jun Zhou, Juan Niu, Yu-Ming |
author_sort | Zhang, Dan-Feng |
collection | PubMed |
description | BACKGROUND: Molecular epidemiological studies have demonstrated a closer association between Fas/FasL polymorphisms and head and neck cancer (HNC) risk, and the results of these published studies were inconsistent. We therefore performed this meta-analysis to explore the associations between Fas/FasL polymorphisms and HNC risk. METHODS: Four online databases (PubMed, Embase, CNKI, and Wanfang) were searched. Odds ratios (ORs) with 95% confidence interval (95% CIs) were calculated to assess the association between Fas -670A>G, Fas -1377G>A, and FasL -844C>T polymorphisms and HNC risk. In addition, heterogeneity, accumulative/sensitivity analysis, and publication bias were conducted to check the statistical power. RESULTS: Overall, 9 related publications (20 independent case–control studies) involving 3179 patients and 4217 controls were identified. Significant association of protective effects was observed between FasL -844C>T polymorphism and HNC risk in codominant and dominant model models (CT vs CC: OR = 0.89, 95% CI = 0.79–1.00, P = .05, I(2) = 38.3%, CT+TT vs CC: OR = 0.88, 95% CI = 0.79–0.98, P = .02, I(2) = 35.8%). Furthermore, the similar protective effects were observed the subgroup analysis of in Asian population and population-based controls group. CONCLUSION: Our meta-analysis indicated that FasL -844C>T polymorphism plays a protective role against HNC development, but the Fas -670A>G and Fas -1377G>A polymorphisms maybe not associated with HNC risk. |
format | Online Article Text |
id | pubmed-5944675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-59446752018-05-17 Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk Zhang, Dan-Feng Jiang, Guang-Bin Qin, Chuan-Qi Liu, De-Xi Hu, Ya-Jun Zhou, Juan Niu, Yu-Ming Medicine (Baltimore) Research Article BACKGROUND: Molecular epidemiological studies have demonstrated a closer association between Fas/FasL polymorphisms and head and neck cancer (HNC) risk, and the results of these published studies were inconsistent. We therefore performed this meta-analysis to explore the associations between Fas/FasL polymorphisms and HNC risk. METHODS: Four online databases (PubMed, Embase, CNKI, and Wanfang) were searched. Odds ratios (ORs) with 95% confidence interval (95% CIs) were calculated to assess the association between Fas -670A>G, Fas -1377G>A, and FasL -844C>T polymorphisms and HNC risk. In addition, heterogeneity, accumulative/sensitivity analysis, and publication bias were conducted to check the statistical power. RESULTS: Overall, 9 related publications (20 independent case–control studies) involving 3179 patients and 4217 controls were identified. Significant association of protective effects was observed between FasL -844C>T polymorphism and HNC risk in codominant and dominant model models (CT vs CC: OR = 0.89, 95% CI = 0.79–1.00, P = .05, I(2) = 38.3%, CT+TT vs CC: OR = 0.88, 95% CI = 0.79–0.98, P = .02, I(2) = 35.8%). Furthermore, the similar protective effects were observed the subgroup analysis of in Asian population and population-based controls group. CONCLUSION: Our meta-analysis indicated that FasL -844C>T polymorphism plays a protective role against HNC development, but the Fas -670A>G and Fas -1377G>A polymorphisms maybe not associated with HNC risk. Wolters Kluwer Health 2018-02-09 /pmc/articles/PMC5944675/ /pubmed/29419701 http://dx.doi.org/10.1097/MD.0000000000009873 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0 |
spellingShingle | Research Article Zhang, Dan-Feng Jiang, Guang-Bin Qin, Chuan-Qi Liu, De-Xi Hu, Ya-Jun Zhou, Juan Niu, Yu-Ming Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk |
title | Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk |
title_full | Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk |
title_fullStr | Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk |
title_full_unstemmed | Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk |
title_short | Quantitative assessment of the relationship between Fas/FasL genes polymorphisms and head and neck cancer risk |
title_sort | quantitative assessment of the relationship between fas/fasl genes polymorphisms and head and neck cancer risk |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944675/ https://www.ncbi.nlm.nih.gov/pubmed/29419701 http://dx.doi.org/10.1097/MD.0000000000009873 |
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