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Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis

Molecular epidemiological research suggests that interleukin-10 (IL-10) polymorphisms may be associated with an increased risk of head and neck cancer (HNC), but results remain controversial. To derive a more precise evaluation, we performed a meta-analysis focused on genetic polymorphisms of IL-10....

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Autores principales: Niu, Yu-Ming, Du, Xin-Ya, Cai, Heng-Xing, Zhang, Chao, Yuan, Rui-Xia, Zeng, Xian-Tao, Luo, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661474/
https://www.ncbi.nlm.nih.gov/pubmed/26612133
http://dx.doi.org/10.1038/srep17149
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author Niu, Yu-Ming
Du, Xin-Ya
Cai, Heng-Xing
Zhang, Chao
Yuan, Rui-Xia
Zeng, Xian-Tao
Luo, Jie
author_facet Niu, Yu-Ming
Du, Xin-Ya
Cai, Heng-Xing
Zhang, Chao
Yuan, Rui-Xia
Zeng, Xian-Tao
Luo, Jie
author_sort Niu, Yu-Ming
collection PubMed
description Molecular epidemiological research suggests that interleukin-10 (IL-10) polymorphisms may be associated with an increased risk of head and neck cancer (HNC), but results remain controversial. To derive a more precise evaluation, we performed a meta-analysis focused on genetic polymorphisms of IL-10. PubMed, Embase, CNKI and Wanfang databases were searched for studies that examined the relationship between IL-10 polymorphisms or haplotypes and HNC risk. The odds ratio (OR) and 95% confidence interval (CI) were applied to assess the relationship strength. Publication bias, sensitivity and cumulative analyses were conducted to measure the robustness of our findings. Overall, nine related studies involving 2,258 patients and 2,887 control samples were analyzed. Significant associations between the IL-10-1082A > G polymorphism and HNC risk were observed (G vs. A: OR = 1.56, 95% CI = 1.27–1.92, P < 0.01, I(2) = 69.4%; AG vs. AA: OR = 1.64, 95% CI = 1.32–2.05, P < 0.01, I(2) = 55.6%; GG vs. AA: OR = 2.24, 95% CI = 1.69–2.97, P < 0.01, I(2) = 38.5%; AG + GG vs. AA: OR = 1.70, 95% CI = 1.36−2.14, P = 0.02, I(2) = 61.8%; GG vs. AA + AG: OR = 1.89, 95% CI = 1.23−2.90, P = 0.01, I(2) = 46.3%) in the total population, as well as in subgroup analysis. Moreover, increased HNC risks were also associated with the IL-10 −819T > C polymorphism and the GCC haplotype. In conclusion, our meta-analyses suggest that IL-10 polymorphisms, specifically the −1082A > G polymorphism, may be associated with increased risk of HNC development.
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spelling pubmed-46614742015-12-02 Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis Niu, Yu-Ming Du, Xin-Ya Cai, Heng-Xing Zhang, Chao Yuan, Rui-Xia Zeng, Xian-Tao Luo, Jie Sci Rep Article Molecular epidemiological research suggests that interleukin-10 (IL-10) polymorphisms may be associated with an increased risk of head and neck cancer (HNC), but results remain controversial. To derive a more precise evaluation, we performed a meta-analysis focused on genetic polymorphisms of IL-10. PubMed, Embase, CNKI and Wanfang databases were searched for studies that examined the relationship between IL-10 polymorphisms or haplotypes and HNC risk. The odds ratio (OR) and 95% confidence interval (CI) were applied to assess the relationship strength. Publication bias, sensitivity and cumulative analyses were conducted to measure the robustness of our findings. Overall, nine related studies involving 2,258 patients and 2,887 control samples were analyzed. Significant associations between the IL-10-1082A > G polymorphism and HNC risk were observed (G vs. A: OR = 1.56, 95% CI = 1.27–1.92, P < 0.01, I(2) = 69.4%; AG vs. AA: OR = 1.64, 95% CI = 1.32–2.05, P < 0.01, I(2) = 55.6%; GG vs. AA: OR = 2.24, 95% CI = 1.69–2.97, P < 0.01, I(2) = 38.5%; AG + GG vs. AA: OR = 1.70, 95% CI = 1.36−2.14, P = 0.02, I(2) = 61.8%; GG vs. AA + AG: OR = 1.89, 95% CI = 1.23−2.90, P = 0.01, I(2) = 46.3%) in the total population, as well as in subgroup analysis. Moreover, increased HNC risks were also associated with the IL-10 −819T > C polymorphism and the GCC haplotype. In conclusion, our meta-analyses suggest that IL-10 polymorphisms, specifically the −1082A > G polymorphism, may be associated with increased risk of HNC development. Nature Publishing Group 2015-11-27 /pmc/articles/PMC4661474/ /pubmed/26612133 http://dx.doi.org/10.1038/srep17149 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Niu, Yu-Ming
Du, Xin-Ya
Cai, Heng-Xing
Zhang, Chao
Yuan, Rui-Xia
Zeng, Xian-Tao
Luo, Jie
Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis
title Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis
title_full Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis
title_fullStr Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis
title_full_unstemmed Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis
title_short Increased risks between Interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis
title_sort increased risks between interleukin-10 gene polymorphisms and haplotype and head and neck cancer: a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661474/
https://www.ncbi.nlm.nih.gov/pubmed/26612133
http://dx.doi.org/10.1038/srep17149
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