Cargando…

The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population

Human 8-oxoguanine DNA glycosylase (hOGG1) is known to play an important role in the prevention of carcinogenesis, including gastric cancer (GC). We performed a case-control study to investigate whether single nucleotide polymorphisms (SNPs) of hOGG1 are associated with GC risk in a Chinese populati...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Jiafei, Yin, Yongmei, Du, Mulong, Ma, Gaoxiang, Ge, Yuqiu, Zhang, Qiang, Chu, Haiyan, Tong, Na, Wang, Meilin, Qiu, Jinrong, Zhang, Zhengdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323214/
https://www.ncbi.nlm.nih.gov/pubmed/27603140
http://dx.doi.org/10.18632/oncotarget.11802
_version_ 1782509992217149440
author Lu, Jiafei
Yin, Yongmei
Du, Mulong
Ma, Gaoxiang
Ge, Yuqiu
Zhang, Qiang
Chu, Haiyan
Tong, Na
Wang, Meilin
Qiu, Jinrong
Zhang, Zhengdong
author_facet Lu, Jiafei
Yin, Yongmei
Du, Mulong
Ma, Gaoxiang
Ge, Yuqiu
Zhang, Qiang
Chu, Haiyan
Tong, Na
Wang, Meilin
Qiu, Jinrong
Zhang, Zhengdong
author_sort Lu, Jiafei
collection PubMed
description Human 8-oxoguanine DNA glycosylase (hOGG1) is known to play an important role in the prevention of carcinogenesis, including gastric cancer (GC). We performed a case-control study to investigate whether single nucleotide polymorphisms (SNPs) of hOGG1 are associated with GC risk in a Chinese population. Two potential functional tagSNPs (rs159153 and rs1052133) and a previously reported risk SNP (rs125701) were genotyped in 1,275 GC patients and 1,436 controls. We found that SNP rs125701 G > A was significantly associated with the increased GC risk [adjusted odds ratio (OR) = 1.38, 95% confidence interval (CI) = 1.05-1.79 in additive model]. Besides, the functional studies demonstrated that the minor A allele of rs125701 significantly reduced the transcriptional activity of hOGG1 promoter and enhanced the methylation level of CpG site of cg15357639. In conclusion, our results suggested that the SNP rs125701 in hOGG1 promoter was associated with the elevated GC risk, which could act as a new potential biomarker for GC susceptibility. Further functional verification of rs125701 in GC pathogenesis is warranted.
format Online
Article
Text
id pubmed-5323214
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-53232142017-03-23 The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population Lu, Jiafei Yin, Yongmei Du, Mulong Ma, Gaoxiang Ge, Yuqiu Zhang, Qiang Chu, Haiyan Tong, Na Wang, Meilin Qiu, Jinrong Zhang, Zhengdong Oncotarget Research Paper Human 8-oxoguanine DNA glycosylase (hOGG1) is known to play an important role in the prevention of carcinogenesis, including gastric cancer (GC). We performed a case-control study to investigate whether single nucleotide polymorphisms (SNPs) of hOGG1 are associated with GC risk in a Chinese population. Two potential functional tagSNPs (rs159153 and rs1052133) and a previously reported risk SNP (rs125701) were genotyped in 1,275 GC patients and 1,436 controls. We found that SNP rs125701 G > A was significantly associated with the increased GC risk [adjusted odds ratio (OR) = 1.38, 95% confidence interval (CI) = 1.05-1.79 in additive model]. Besides, the functional studies demonstrated that the minor A allele of rs125701 significantly reduced the transcriptional activity of hOGG1 promoter and enhanced the methylation level of CpG site of cg15357639. In conclusion, our results suggested that the SNP rs125701 in hOGG1 promoter was associated with the elevated GC risk, which could act as a new potential biomarker for GC susceptibility. Further functional verification of rs125701 in GC pathogenesis is warranted. Impact Journals LLC 2016-09-01 /pmc/articles/PMC5323214/ /pubmed/27603140 http://dx.doi.org/10.18632/oncotarget.11802 Text en Copyright: © 2016 Lu et al. http://creativecommons.org/licenses/by/2.5/ 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
Lu, Jiafei
Yin, Yongmei
Du, Mulong
Ma, Gaoxiang
Ge, Yuqiu
Zhang, Qiang
Chu, Haiyan
Tong, Na
Wang, Meilin
Qiu, Jinrong
Zhang, Zhengdong
The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population
title The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population
title_full The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population
title_fullStr The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population
title_full_unstemmed The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population
title_short The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population
title_sort association analysis of hogg1 genetic variants and gastric cancer risk in a chinese population
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323214/
https://www.ncbi.nlm.nih.gov/pubmed/27603140
http://dx.doi.org/10.18632/oncotarget.11802
work_keys_str_mv AT lujiafei theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT yinyongmei theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT dumulong theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT magaoxiang theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT geyuqiu theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT zhangqiang theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT chuhaiyan theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT tongna theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT wangmeilin theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT qiujinrong theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT zhangzhengdong theassociationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT lujiafei associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT yinyongmei associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT dumulong associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT magaoxiang associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT geyuqiu associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT zhangqiang associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT chuhaiyan associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT tongna associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT wangmeilin associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT qiujinrong associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation
AT zhangzhengdong associationanalysisofhogg1geneticvariantsandgastriccancerriskinachinesepopulation