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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...
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/PMC5323214/ https://www.ncbi.nlm.nih.gov/pubmed/27603140 http://dx.doi.org/10.18632/oncotarget.11802 |
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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 |
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