The miR-184 binding-site rs8126 T>C polymorphism in TNFAIP2 is associated with risk of gastric cancer.
Abstract
TNFAIP2 is a crucial gene involved in apoptosis. Single nucleotide polymorphisms (SNPs)
in its miRNA binding sites could modulate functions of the miRNA-target genes and
thus risk of cancers. In this study, we investigated associations between potentially
functional SNPs in the miRNA binding sites of the 3'UTR of TNFAIP2 and gastric cancer
risk in a US population.We conducted a case-control study of 301 gastric cancer patients
and 313 cancer-free controls frequency-matched by age, sex and ethnicity. We genotyped
four selected TNFAIP2 SNPs (rs8126 T>C, rs710100 G>A, rs1052912 G>A and rs1052823
G>T) and used the logistic regression analysis to assess associations of these SNPs
with cancer risk.The rs8126 CC genotype was associated with a significantly elevated
risk of gastric cancer (adjusted OR = 2.00, 95% CI = 1.09-3.64 and P = 0.024), compared
with the combined rs8126 TT+TC genotypes, particularly in current drinkers. However,
none of other TNFAIP2 SNPs was associated with risk of gastric cancer.Our data suggested
that the TNFAIP2 miRNA binding site rs8126 T>C SNP may be a marker for susceptibility
to gastric cancer, and this finding requires further validation by larger studies.
Type
Journal articleSubject
HumansStomach Neoplasms
Genetic Predisposition to Disease
MicroRNAs
Cytokines
Logistic Models
Risk Factors
Demography
Binding Sites
Haplotypes
Polymorphism, Single Nucleotide
Middle Aged
Female
Male
Genetic Association Studies
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https://hdl.handle.net/10161/18023Published Version (Please cite this version)
10.1371/journal.pone.0064973Publication Info
Xu, Yu; Ma, Hongxia; Yu, Hongping; Liu, Zhensheng; Wang, Li-E; Tan, Dongfeng; ...
Wei, Qingyi (2013). The miR-184 binding-site rs8126 T>C polymorphism in TNFAIP2 is associated with risk
of gastric cancer. PloS one, 8(5). pp. e64973. 10.1371/journal.pone.0064973. Retrieved from https://hdl.handle.net/10161/18023.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Zhensheng Liu
Assistant Professor of Medicine
Qingyi Wei
Professor in Population Health Sciences
Qingyi Wei, MD, PhD, Professor in the Department of Medicine, is Associate Director
for Cancer Control and Population Sciences, Co-leader of CCPS and Co-leader of Epidemiology
and Population Genomics (Focus Area 1). He is a professor of Medicine and an internationally
recognized epidemiologist focused on the molecular and genetic epidemiology of head
and neck cancers, lung cancer, and melanoma. His research focuses on biomarkers and
genetic determinants for the DNA repair deficient phenotype and
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