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Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women

Genetic variations in transcription factor 7-like 2 (TCF7L2) are associated with cancer risk. This study was conducted to establish the relationship between TCF7L2 polymorphisms (rs1225404, rs7003146, and rs7903146) and clinical features and risk of breast cancer in Northwest Chinese Han women. In t...

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Autores principales: Min, Weili, Liu, Xinghan, Lu, Ye, Gong, Zhuoqing, Wang, Meng, Lin, Shuai, Kang, Huafeng, Jin, Tianbo, Wang, Xijing, Ma, Xiaobin, Liu, Kang, Dai, Cong, Zheng, Yi, Li, Shanli, Ma, Qingyong, Dai, Zhijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363578/
https://www.ncbi.nlm.nih.gov/pubmed/27738320
http://dx.doi.org/10.18632/oncotarget.12591
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author Min, Weili
Liu, Xinghan
Lu, Ye
Gong, Zhuoqing
Wang, Meng
Lin, Shuai
Kang, Huafeng
Jin, Tianbo
Wang, Xijing
Ma, Xiaobin
Liu, Kang
Dai, Cong
Zheng, Yi
Li, Shanli
Ma, Qingyong
Dai, Zhijun
author_facet Min, Weili
Liu, Xinghan
Lu, Ye
Gong, Zhuoqing
Wang, Meng
Lin, Shuai
Kang, Huafeng
Jin, Tianbo
Wang, Xijing
Ma, Xiaobin
Liu, Kang
Dai, Cong
Zheng, Yi
Li, Shanli
Ma, Qingyong
Dai, Zhijun
author_sort Min, Weili
collection PubMed
description Genetic variations in transcription factor 7-like 2 (TCF7L2) are associated with cancer risk. This study was conducted to establish the relationship between TCF7L2 polymorphisms (rs1225404, rs7003146, and rs7903146) and clinical features and risk of breast cancer in Northwest Chinese Han women. In this study, three polymorphisms of TCF7L2 (rs1225404, rs7003146, and rs7903146) were genotyped in 458 patients with breast cancer and 500 healthy controls using the Sequenom MassARRAY-iPLEX system. We evaluated the associations between the polymorphisms and breast cancer using odds ratios (ORs) and corresponding 95% confidence intervals (95% CIs). The C allele of rs1225404 was associated with increased breast cancer risk (OR = 1.58, P = 0.0004, P(C)= 0.0012), whereas the G allele of rs7003146 was associated with decreased breast cancer risk (OR = 0.71, P = 0.01, P(C)= 0.03). Furthermore, the rs1225404 polymorphism positively correlated with negative progesterone receptor status. A positive correlation with positive estrogen receptor (ER) status was observed for the rs7003146 polymorphism. Our results suggest that TCF7L2 polymorphisms rs1225404 and rs7003146, but not rs7903146, may affect breast cancer risk in Northwest Chinese women. Additionally, the tag polymorphisms in TCF7L2 are associated with the clinical features of breast cancer, which may provide us novel insight into the pathogenesis of breast cancer.
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spelling pubmed-53635782017-03-29 Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women Min, Weili Liu, Xinghan Lu, Ye Gong, Zhuoqing Wang, Meng Lin, Shuai Kang, Huafeng Jin, Tianbo Wang, Xijing Ma, Xiaobin Liu, Kang Dai, Cong Zheng, Yi Li, Shanli Ma, Qingyong Dai, Zhijun Oncotarget Research Paper Genetic variations in transcription factor 7-like 2 (TCF7L2) are associated with cancer risk. This study was conducted to establish the relationship between TCF7L2 polymorphisms (rs1225404, rs7003146, and rs7903146) and clinical features and risk of breast cancer in Northwest Chinese Han women. In this study, three polymorphisms of TCF7L2 (rs1225404, rs7003146, and rs7903146) were genotyped in 458 patients with breast cancer and 500 healthy controls using the Sequenom MassARRAY-iPLEX system. We evaluated the associations between the polymorphisms and breast cancer using odds ratios (ORs) and corresponding 95% confidence intervals (95% CIs). The C allele of rs1225404 was associated with increased breast cancer risk (OR = 1.58, P = 0.0004, P(C)= 0.0012), whereas the G allele of rs7003146 was associated with decreased breast cancer risk (OR = 0.71, P = 0.01, P(C)= 0.03). Furthermore, the rs1225404 polymorphism positively correlated with negative progesterone receptor status. A positive correlation with positive estrogen receptor (ER) status was observed for the rs7003146 polymorphism. Our results suggest that TCF7L2 polymorphisms rs1225404 and rs7003146, but not rs7903146, may affect breast cancer risk in Northwest Chinese women. Additionally, the tag polymorphisms in TCF7L2 are associated with the clinical features of breast cancer, which may provide us novel insight into the pathogenesis of breast cancer. Impact Journals LLC 2016-10-12 /pmc/articles/PMC5363578/ /pubmed/27738320 http://dx.doi.org/10.18632/oncotarget.12591 Text en Copyright: © 2016 Min et al. http://creativecommons.org/licenses/by/3.0/ 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 credited.
spellingShingle Research Paper
Min, Weili
Liu, Xinghan
Lu, Ye
Gong, Zhuoqing
Wang, Meng
Lin, Shuai
Kang, Huafeng
Jin, Tianbo
Wang, Xijing
Ma, Xiaobin
Liu, Kang
Dai, Cong
Zheng, Yi
Li, Shanli
Ma, Qingyong
Dai, Zhijun
Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women
title Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women
title_full Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women
title_fullStr Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women
title_full_unstemmed Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women
title_short Association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest Chinese women
title_sort association of transcription factor 7-like 2 gene polymorphisms with breast cancer risk in northwest chinese women
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363578/
https://www.ncbi.nlm.nih.gov/pubmed/27738320
http://dx.doi.org/10.18632/oncotarget.12591
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