Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer

Genetic variants in human microRNA (miRNA) genes may alter mature miRNA processing and/or target selection, and likely contribute to cancer susceptibility and disease progression. Previous studies have suggested that miR-101 may play important roles in the development of cancer by regulating key tum...

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Main Authors: Chen, Jiaping, Qin, Zhenzhen, Jiang, Yue, Wang, Yanru, He, Yisha, Dai, Juncheng, Jin, Guangfu, Ma, Hongxia, Hu, Zhibin, Yin, Yongmei, Shen, Hongbing
Format: Online
Language:English
Published: Public Library of Science 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901682/
id pubmed-3901682
recordtype oai_dc
spelling pubmed-39016822014-01-28 Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer Chen, Jiaping Qin, Zhenzhen Jiang, Yue Wang, Yanru He, Yisha Dai, Juncheng Jin, Guangfu Ma, Hongxia Hu, Zhibin Yin, Yongmei Shen, Hongbing Research Article Genetic variants in human microRNA (miRNA) genes may alter mature miRNA processing and/or target selection, and likely contribute to cancer susceptibility and disease progression. Previous studies have suggested that miR-101 may play important roles in the development of cancer by regulating key tumor-associated genes. However, the role of single nucleotide polymorphisms (SNPs) of miR-101 in breast cancer susceptibility remains unclear. In this study, we genotyped 11 SNPs of the miR-101 genes (including miR-101-1 and miR-101-2) in a case-control study of 1064 breast cancer cases and 1073 cancer-free controls. The results revealed that rs462480 and rs1053872 in the flank regions of pre-miR-101-2 were significantly associated with increased risk of breast cancer (rs462480 AC/CC vs AA: adjusted OR = 1.182, 95% CI: 1.030–1.357, P = 0.017; rs1053872 CG/GG vs CC: adjusted OR = 1.179, 95% CI: 1.040–1.337, P = 0.010). However, the remaining 9 SNPs were not significantly associated with risk of breast cancer. Additionally, combined analysis of the two high-risk SNPs revealed that subjects carrying the variant genotypes of rs462480 and rs1053872 had increased risk of breast cancer in a dose-response manner (P trend = 0.002). Compared with individuals with “0–1” risk allele, those carrying “2–4” risk alleles had 1.29-fold risk of breast cancer. In conclusion, these findings suggested that the SNPs rs462480 and rs1053872 residing in miR-101-2 gene may have a solid impact on genetic susceptibility to breast cancer, which may improve our understanding of the potential contribution of miRNA SNPs to cancer pathogenesis. Public Library of Science 2014-01-24 /pmc/articles/PMC3901682/ /pubmed/24475105 http://dx.doi.org/10.1371/journal.pone.0086319 Text en © 2014 Chen 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.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Chen, Jiaping
Qin, Zhenzhen
Jiang, Yue
Wang, Yanru
He, Yisha
Dai, Juncheng
Jin, Guangfu
Ma, Hongxia
Hu, Zhibin
Yin, Yongmei
Shen, Hongbing
spellingShingle Chen, Jiaping
Qin, Zhenzhen
Jiang, Yue
Wang, Yanru
He, Yisha
Dai, Juncheng
Jin, Guangfu
Ma, Hongxia
Hu, Zhibin
Yin, Yongmei
Shen, Hongbing
Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
author_facet Chen, Jiaping
Qin, Zhenzhen
Jiang, Yue
Wang, Yanru
He, Yisha
Dai, Juncheng
Jin, Guangfu
Ma, Hongxia
Hu, Zhibin
Yin, Yongmei
Shen, Hongbing
author_sort Chen, Jiaping
title Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
title_short Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
title_full Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
title_fullStr Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
title_full_unstemmed Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
title_sort genetic variations in the flanking regions of mir-101-2 are associated with increased risk of breast cancer
description Genetic variants in human microRNA (miRNA) genes may alter mature miRNA processing and/or target selection, and likely contribute to cancer susceptibility and disease progression. Previous studies have suggested that miR-101 may play important roles in the development of cancer by regulating key tumor-associated genes. However, the role of single nucleotide polymorphisms (SNPs) of miR-101 in breast cancer susceptibility remains unclear. In this study, we genotyped 11 SNPs of the miR-101 genes (including miR-101-1 and miR-101-2) in a case-control study of 1064 breast cancer cases and 1073 cancer-free controls. The results revealed that rs462480 and rs1053872 in the flank regions of pre-miR-101-2 were significantly associated with increased risk of breast cancer (rs462480 AC/CC vs AA: adjusted OR = 1.182, 95% CI: 1.030–1.357, P = 0.017; rs1053872 CG/GG vs CC: adjusted OR = 1.179, 95% CI: 1.040–1.337, P = 0.010). However, the remaining 9 SNPs were not significantly associated with risk of breast cancer. Additionally, combined analysis of the two high-risk SNPs revealed that subjects carrying the variant genotypes of rs462480 and rs1053872 had increased risk of breast cancer in a dose-response manner (P trend = 0.002). Compared with individuals with “0–1” risk allele, those carrying “2–4” risk alleles had 1.29-fold risk of breast cancer. In conclusion, these findings suggested that the SNPs rs462480 and rs1053872 residing in miR-101-2 gene may have a solid impact on genetic susceptibility to breast cancer, which may improve our understanding of the potential contribution of miRNA SNPs to cancer pathogenesis.
publisher Public Library of Science
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901682/
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