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Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects

The relationship between cyclin D1 (CCND1) rs9344 G>A polymorphism and colorectal cancer (CRC) risk is still ambiguous. To obtain a precise estimation of the relationship, we performed an extensive meta-analysis based on the eligible studies. Crude odds ratios with their 95% confidence intervals...

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Autores principales: Qiu, Hao, Cheng, Chengguo, Wang, Yafeng, Kang, Mingqiang, Tang, Weifeng, Chen, Shuchen, Gu, Haiyong, Liu, Chao, Chen, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089821/
https://www.ncbi.nlm.nih.gov/pubmed/27822068
http://dx.doi.org/10.2147/OTT.S116258
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author Qiu, Hao
Cheng, Chengguo
Wang, Yafeng
Kang, Mingqiang
Tang, Weifeng
Chen, Shuchen
Gu, Haiyong
Liu, Chao
Chen, Yu
author_facet Qiu, Hao
Cheng, Chengguo
Wang, Yafeng
Kang, Mingqiang
Tang, Weifeng
Chen, Shuchen
Gu, Haiyong
Liu, Chao
Chen, Yu
author_sort Qiu, Hao
collection PubMed
description The relationship between cyclin D1 (CCND1) rs9344 G>A polymorphism and colorectal cancer (CRC) risk is still ambiguous. To obtain a precise estimation of the relationship, we performed an extensive meta-analysis based on the eligible studies. Crude odds ratios with their 95% confidence intervals were harnessed to determine the strength of correlation between CCND1 rs9344 G>A polymorphism and CRC risk under the allele, the homozygote, the dominant, and the recessive genetic models, respectively (28 studies with 5,784 CRC cases and 7,858 controls). Our results indicated evidence of the association between CCND1 rs9344 G>A polymorphism and the increased risk of CRC in four genetic models: A vs G, AA vs GG, AA+GA vs GG, and AA vs GA+GG. In a stratified analysis by cancer type of CRC, there was an increased risk of sporadic CRC found in three genetic models: A vs G, AA vs GG, and AA+GA vs GG. In a stratified analysis by ethnicity, there was an increased CRC risk found among Asians in allele comparison genetic models, as well as Caucasians in two genetic models: AA+GA vs GG and A vs T. In summary, this meta-analysis demonstrates that CCND1 rs9344 G>A polymorphism may be a risk factor for CRC.
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spelling pubmed-50898212016-11-07 Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects Qiu, Hao Cheng, Chengguo Wang, Yafeng Kang, Mingqiang Tang, Weifeng Chen, Shuchen Gu, Haiyong Liu, Chao Chen, Yu Onco Targets Ther Original Research The relationship between cyclin D1 (CCND1) rs9344 G>A polymorphism and colorectal cancer (CRC) risk is still ambiguous. To obtain a precise estimation of the relationship, we performed an extensive meta-analysis based on the eligible studies. Crude odds ratios with their 95% confidence intervals were harnessed to determine the strength of correlation between CCND1 rs9344 G>A polymorphism and CRC risk under the allele, the homozygote, the dominant, and the recessive genetic models, respectively (28 studies with 5,784 CRC cases and 7,858 controls). Our results indicated evidence of the association between CCND1 rs9344 G>A polymorphism and the increased risk of CRC in four genetic models: A vs G, AA vs GG, AA+GA vs GG, and AA vs GA+GG. In a stratified analysis by cancer type of CRC, there was an increased risk of sporadic CRC found in three genetic models: A vs G, AA vs GG, and AA+GA vs GG. In a stratified analysis by ethnicity, there was an increased CRC risk found among Asians in allele comparison genetic models, as well as Caucasians in two genetic models: AA+GA vs GG and A vs T. In summary, this meta-analysis demonstrates that CCND1 rs9344 G>A polymorphism may be a risk factor for CRC. Dove Medical Press 2016-10-27 /pmc/articles/PMC5089821/ /pubmed/27822068 http://dx.doi.org/10.2147/OTT.S116258 Text en © 2016 Qiu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Qiu, Hao
Cheng, Chengguo
Wang, Yafeng
Kang, Mingqiang
Tang, Weifeng
Chen, Shuchen
Gu, Haiyong
Liu, Chao
Chen, Yu
Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects
title Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects
title_full Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects
title_fullStr Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects
title_full_unstemmed Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects
title_short Investigation of cyclin D1 rs9344 G>A polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects
title_sort investigation of cyclin d1 rs9344 g>a polymorphism in colorectal cancer: a meta-analysis involving 13,642 subjects
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089821/
https://www.ncbi.nlm.nih.gov/pubmed/27822068
http://dx.doi.org/10.2147/OTT.S116258
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