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Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk

Genome-wide association studies (GWAS) have identified several genetic susceptibility loci for breast cancer (BC). One of them, conducted among Chinese women, found an association of rs2046210 at 6q25.1 with the risk of BC recently. Since then, numerous association studies have been carried out to i...

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Autores principales: Wu, Xi, Xu, Qing-Qing, Guo, Liang, Yu, Chuan-Ting, Xiong, Yu-Yu, Wei, Zhi-Yun, Huo, Ran, Li, Sheng-Tian, Shen, Lu, Niu, Jia-Min, Liu, Lu, Lin, Yi, He, Lin, Qin, Sheng-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681980/
https://www.ncbi.nlm.nih.gov/pubmed/23785413
http://dx.doi.org/10.1371/journal.pone.0065206
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author Wu, Xi
Xu, Qing-Qing
Guo, Liang
Yu, Chuan-Ting
Xiong, Yu-Yu
Wei, Zhi-Yun
Huo, Ran
Li, Sheng-Tian
Shen, Lu
Niu, Jia-Min
Liu, Lu
Lin, Yi
He, Lin
Qin, Sheng-Ying
author_facet Wu, Xi
Xu, Qing-Qing
Guo, Liang
Yu, Chuan-Ting
Xiong, Yu-Yu
Wei, Zhi-Yun
Huo, Ran
Li, Sheng-Tian
Shen, Lu
Niu, Jia-Min
Liu, Lu
Lin, Yi
He, Lin
Qin, Sheng-Ying
author_sort Wu, Xi
collection PubMed
description Genome-wide association studies (GWAS) have identified several genetic susceptibility loci for breast cancer (BC). One of them, conducted among Chinese women, found an association of rs2046210 at 6q25.1 with the risk of BC recently. Since then, numerous association studies have been carried out to investigate the relationship between this polymorphism and BC risk in various populations. However, these have yielded contradictory results. We therefore performed a meta-analysis to clarify this inconsistency. Overall, a total of 235003 subjects based on 13 studies were included in our study. Significantly increased BC risk was detected in the pooled analysis [allele contrast: OR = 1.13, 95%CI = 1.10–1.17, P(Z) <10(−5), P(Q) <10(−4); dominant model: OR = 1.21, 95%CI = 1.14–1.27, P(Z) <10(−5), P(Q) <10(−4); recessive model: OR = 1.18, 95%CI = 1.12–1.24, P(Z) <10(−5), P(Q) = 0.04]. In addition, our data revealed that rs2046210 conferred greater risk in estrogen receptor (ER)-negative tumors [OR = 1.27, 95%CI = 1.15–1.40, P(Z) <10(−5), P(Q) <10(−4)] than in ER-positive ones [OR = 1.18, 95%CI = 1.09–1.28, P(Z) <10(−4), P(Q) = 0.0003]. When stratified by ethnicity, significant associations were found in Caucasian and Asian populations, but not detected among Africans. There was evidence of heterogeneity (P<0.05), however, the heterogeneity largely disappeared after stratification by ethnicity. The present meta-analysis demonstrated that the rs2046210 polymorphism may be associated with increased BC susceptibility, but this association varies in different ethnicities.
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spelling pubmed-36819802013-06-19 Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk Wu, Xi Xu, Qing-Qing Guo, Liang Yu, Chuan-Ting Xiong, Yu-Yu Wei, Zhi-Yun Huo, Ran Li, Sheng-Tian Shen, Lu Niu, Jia-Min Liu, Lu Lin, Yi He, Lin Qin, Sheng-Ying PLoS One Research Article Genome-wide association studies (GWAS) have identified several genetic susceptibility loci for breast cancer (BC). One of them, conducted among Chinese women, found an association of rs2046210 at 6q25.1 with the risk of BC recently. Since then, numerous association studies have been carried out to investigate the relationship between this polymorphism and BC risk in various populations. However, these have yielded contradictory results. We therefore performed a meta-analysis to clarify this inconsistency. Overall, a total of 235003 subjects based on 13 studies were included in our study. Significantly increased BC risk was detected in the pooled analysis [allele contrast: OR = 1.13, 95%CI = 1.10–1.17, P(Z) <10(−5), P(Q) <10(−4); dominant model: OR = 1.21, 95%CI = 1.14–1.27, P(Z) <10(−5), P(Q) <10(−4); recessive model: OR = 1.18, 95%CI = 1.12–1.24, P(Z) <10(−5), P(Q) = 0.04]. In addition, our data revealed that rs2046210 conferred greater risk in estrogen receptor (ER)-negative tumors [OR = 1.27, 95%CI = 1.15–1.40, P(Z) <10(−5), P(Q) <10(−4)] than in ER-positive ones [OR = 1.18, 95%CI = 1.09–1.28, P(Z) <10(−4), P(Q) = 0.0003]. When stratified by ethnicity, significant associations were found in Caucasian and Asian populations, but not detected among Africans. There was evidence of heterogeneity (P<0.05), however, the heterogeneity largely disappeared after stratification by ethnicity. The present meta-analysis demonstrated that the rs2046210 polymorphism may be associated with increased BC susceptibility, but this association varies in different ethnicities. Public Library of Science 2013-06-13 /pmc/articles/PMC3681980/ /pubmed/23785413 http://dx.doi.org/10.1371/journal.pone.0065206 Text en © 2013 Wu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wu, Xi
Xu, Qing-Qing
Guo, Liang
Yu, Chuan-Ting
Xiong, Yu-Yu
Wei, Zhi-Yun
Huo, Ran
Li, Sheng-Tian
Shen, Lu
Niu, Jia-Min
Liu, Lu
Lin, Yi
He, Lin
Qin, Sheng-Ying
Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk
title Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk
title_full Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk
title_fullStr Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk
title_full_unstemmed Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk
title_short Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk
title_sort quantitative assessment of the association between rs2046210 at 6q25.1 and breast cancer risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681980/
https://www.ncbi.nlm.nih.gov/pubmed/23785413
http://dx.doi.org/10.1371/journal.pone.0065206
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