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Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis

Vitamin D receptor (VDR) Cdx-2 polymorphism (rs11568820) has been indicated to be associated to cancer susceptibility. However, published studies reported mixed results. This meta-analysis was conducted to get a more accurate estimation of the association between Cdx-2 polymorphism and cancer risk....

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Autores principales: Dai, Zhi-Ming, Fei, Yu-Lang, Zhang, Wang-Gang, Liu, Jie, Cao, Xing-Mei, Qu, Qiu-Min, Li, Yan-Chun, Lin, Shuai, Wang, Meng, Dai, Zhi-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616440/
https://www.ncbi.nlm.nih.gov/pubmed/26287424
http://dx.doi.org/10.1097/MD.0000000000001370
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author Dai, Zhi-Ming
Fei, Yu-Lang
Zhang, Wang-Gang
Liu, Jie
Cao, Xing-Mei
Qu, Qiu-Min
Li, Yan-Chun
Lin, Shuai
Wang, Meng
Dai, Zhi-Jun
author_facet Dai, Zhi-Ming
Fei, Yu-Lang
Zhang, Wang-Gang
Liu, Jie
Cao, Xing-Mei
Qu, Qiu-Min
Li, Yan-Chun
Lin, Shuai
Wang, Meng
Dai, Zhi-Jun
author_sort Dai, Zhi-Ming
collection PubMed
description Vitamin D receptor (VDR) Cdx-2 polymorphism (rs11568820) has been indicated to be associated to cancer susceptibility. However, published studies reported mixed results. This meta-analysis was conducted to get a more accurate estimation of the association between Cdx-2 polymorphism and cancer risk. We identified 25 independent studies with a total of 34,018 subjects published prior to March 2015. Summary odds ratios (ORs) and 95% confidence intervals (CIs) were used to evaluate the susceptibility to cancer. Separate analyses were conducted on features of the population such as ethnicity, source of controls, and cancer types. Meta-analysis results showed that Cdx-2 polymorphism significantly increased cancer risk in the homozygous model in overall analysis. According to the further stratified analysis, significant association was found between Cdx-2 variant and cancer risk in American-Africans in the homozygous, recessive, and dominant comparison models. However, no significant associations were found in Caucasians and Asians. When stratified by different cancer types, significant association was observed between Cdx-2 variant and an increased risk of colorectal cancer in the homozygous, recessive, and dominant models. In addition, ovarian cancer susceptibility increased based on the homozygous and dominant comparison models. Our study indicated that VDR Cdx-2 polymorphism was associated with an increased cancer risk, particularly in American-Africans, colorectal, and ovarian cancers. However, other factors may impact on the association. Further multicenter studies are needed to confirm the effects of Cdx-2 polymorphism on cancer susceptibility.
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spelling pubmed-46164402015-10-27 Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis Dai, Zhi-Ming Fei, Yu-Lang Zhang, Wang-Gang Liu, Jie Cao, Xing-Mei Qu, Qiu-Min Li, Yan-Chun Lin, Shuai Wang, Meng Dai, Zhi-Jun Medicine (Baltimore) 3500 Vitamin D receptor (VDR) Cdx-2 polymorphism (rs11568820) has been indicated to be associated to cancer susceptibility. However, published studies reported mixed results. This meta-analysis was conducted to get a more accurate estimation of the association between Cdx-2 polymorphism and cancer risk. We identified 25 independent studies with a total of 34,018 subjects published prior to March 2015. Summary odds ratios (ORs) and 95% confidence intervals (CIs) were used to evaluate the susceptibility to cancer. Separate analyses were conducted on features of the population such as ethnicity, source of controls, and cancer types. Meta-analysis results showed that Cdx-2 polymorphism significantly increased cancer risk in the homozygous model in overall analysis. According to the further stratified analysis, significant association was found between Cdx-2 variant and cancer risk in American-Africans in the homozygous, recessive, and dominant comparison models. However, no significant associations were found in Caucasians and Asians. When stratified by different cancer types, significant association was observed between Cdx-2 variant and an increased risk of colorectal cancer in the homozygous, recessive, and dominant models. In addition, ovarian cancer susceptibility increased based on the homozygous and dominant comparison models. Our study indicated that VDR Cdx-2 polymorphism was associated with an increased cancer risk, particularly in American-Africans, colorectal, and ovarian cancers. However, other factors may impact on the association. Further multicenter studies are needed to confirm the effects of Cdx-2 polymorphism on cancer susceptibility. Wolters Kluwer Health 2015-08-21 /pmc/articles/PMC4616440/ /pubmed/26287424 http://dx.doi.org/10.1097/MD.0000000000001370 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial License, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be used commercially. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 3500
Dai, Zhi-Ming
Fei, Yu-Lang
Zhang, Wang-Gang
Liu, Jie
Cao, Xing-Mei
Qu, Qiu-Min
Li, Yan-Chun
Lin, Shuai
Wang, Meng
Dai, Zhi-Jun
Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis
title Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis
title_full Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis
title_fullStr Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis
title_full_unstemmed Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis
title_short Association of Vitamin D Receptor Cdx-2 Polymorphism With Cancer Risk: A Meta-Analysis
title_sort association of vitamin d receptor cdx-2 polymorphism with cancer risk: a meta-analysis
topic 3500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616440/
https://www.ncbi.nlm.nih.gov/pubmed/26287424
http://dx.doi.org/10.1097/MD.0000000000001370
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