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FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study
This study aimed to assess the associations of two common Flap endonuclease 1 (FEN1) polymorphisms (rs4246215 and rs174538) with breast cancer risk in northwest Chinese women. We conducted a case-control study with 560 breast cancer patients and 583 age-matched healthy controls from Northwest China....
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363647/ https://www.ncbi.nlm.nih.gov/pubmed/27801669 http://dx.doi.org/10.18632/oncotarget.12948 |
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author | Lin, Shuai Wang, Meng Liu, Xinghan Lu, Ye Gong, Zhuoqing Guo, Yan Yang, Pengtao Tian, Tian Dai, Cong Zheng, Yi Xu, Peng Li, Shanli Zhu, Yuyao Dai, Zhijun |
author_facet | Lin, Shuai Wang, Meng Liu, Xinghan Lu, Ye Gong, Zhuoqing Guo, Yan Yang, Pengtao Tian, Tian Dai, Cong Zheng, Yi Xu, Peng Li, Shanli Zhu, Yuyao Dai, Zhijun |
author_sort | Lin, Shuai |
collection | PubMed |
description | This study aimed to assess the associations of two common Flap endonuclease 1 (FEN1) polymorphisms (rs4246215 and rs174538) with breast cancer risk in northwest Chinese women. We conducted a case-control study with 560 breast cancer patients and 583 age-matched healthy controls from Northwest China. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were used to estimate the associations. We found a significantly reduced risk of breast cancer associated with T allele of rs4246215 (allele model: OR 0.81, 95% CI 0.68–0.96; homozygote model: OR = 0.59, 95% CI = 0.40–0.87; recessive model: OR = 0.61, 95% CI = 0.42–0.89), especially in postmenopausal women (OR = 0.58, 95% CI = 0.35–0.97). Furthermore, the polymorphism showed a decreased association with larger tumor size (heterozygote model: OR = 0.63, 95% CI = 0.44–0.92; dominant model: OR = 0.63, 95% CI = 0.44–0.90). For rs174538, we did not find any difference in all genetic models. However, rs174538 was associated with lymph node metastasis (heterozygote model: OR = 0.57, 95% CI = 0.39–0.81; dominant model: OR = 0.61, 95% CI = 0.43–0.86) and estrogen receptor status (heterozygote model: OR = 1.50, 95% CI = 1.05–2.15; dominant model: OR = 1.42, 95% CI = 1.01–1.98). Haplotype analysis showed that T(rs4246215)G(rs174538) haplotype was a protective factor of breast cancer (OR = 0.34, 95% CI = 0.14–0.81). Our results suggest that FEN1 polymorphisms may reduce the risk of breast cancer in Chinese women. |
format | Online Article Text |
id | pubmed-5363647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53636472017-03-29 FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study Lin, Shuai Wang, Meng Liu, Xinghan Lu, Ye Gong, Zhuoqing Guo, Yan Yang, Pengtao Tian, Tian Dai, Cong Zheng, Yi Xu, Peng Li, Shanli Zhu, Yuyao Dai, Zhijun Oncotarget Research Paper This study aimed to assess the associations of two common Flap endonuclease 1 (FEN1) polymorphisms (rs4246215 and rs174538) with breast cancer risk in northwest Chinese women. We conducted a case-control study with 560 breast cancer patients and 583 age-matched healthy controls from Northwest China. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were used to estimate the associations. We found a significantly reduced risk of breast cancer associated with T allele of rs4246215 (allele model: OR 0.81, 95% CI 0.68–0.96; homozygote model: OR = 0.59, 95% CI = 0.40–0.87; recessive model: OR = 0.61, 95% CI = 0.42–0.89), especially in postmenopausal women (OR = 0.58, 95% CI = 0.35–0.97). Furthermore, the polymorphism showed a decreased association with larger tumor size (heterozygote model: OR = 0.63, 95% CI = 0.44–0.92; dominant model: OR = 0.63, 95% CI = 0.44–0.90). For rs174538, we did not find any difference in all genetic models. However, rs174538 was associated with lymph node metastasis (heterozygote model: OR = 0.57, 95% CI = 0.39–0.81; dominant model: OR = 0.61, 95% CI = 0.43–0.86) and estrogen receptor status (heterozygote model: OR = 1.50, 95% CI = 1.05–2.15; dominant model: OR = 1.42, 95% CI = 1.01–1.98). Haplotype analysis showed that T(rs4246215)G(rs174538) haplotype was a protective factor of breast cancer (OR = 0.34, 95% CI = 0.14–0.81). Our results suggest that FEN1 polymorphisms may reduce the risk of breast cancer in Chinese women. Impact Journals LLC 2016-10-27 /pmc/articles/PMC5363647/ /pubmed/27801669 http://dx.doi.org/10.18632/oncotarget.12948 Text en Copyright: © 2016 Lin 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 Lin, Shuai Wang, Meng Liu, Xinghan Lu, Ye Gong, Zhuoqing Guo, Yan Yang, Pengtao Tian, Tian Dai, Cong Zheng, Yi Xu, Peng Li, Shanli Zhu, Yuyao Dai, Zhijun FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study |
title | FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study |
title_full | FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study |
title_fullStr | FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study |
title_full_unstemmed | FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study |
title_short | FEN1 gene variants confer reduced risk of breast cancer in chinese women: A case-control study |
title_sort | fen1 gene variants confer reduced risk of breast cancer in chinese women: a case-control study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363647/ https://www.ncbi.nlm.nih.gov/pubmed/27801669 http://dx.doi.org/10.18632/oncotarget.12948 |
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