Source:http://linkedlifedata.com/resource/pubmed/id/20607725
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2010-9-22
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pubmed:abstractText |
Interleukin-23 receptor (IL-23R) is a key element in T helper (Th)17 cell-mediated inflammatory process, which plays an important role in pathogenesis of gastric cancer. Genetic variants of IL-23R have been identified as the predisposing factors for immunopathologic process. In this study, we hypothesized that the functional genetic variants of IL-23R gene may modify the risk of gastric cancer. To test this hypothesis, we conducted a case-control study including 1043 gastric cancer patients and 1089 controls in a Chinese population to assess the association between two potentially functional single nucleotide polymorphisms (SNPs) rs6682925 T>C and rs1884444 T>G of IL-23R and risk of gastric cancer. We found that the variant allele (G) of rs1884444 T>G, with amino acid His substituted by Gln at codon 3, was significantly associated with a decreased risk of gastric cancer [adjusted allelic odds ratio (OR)?= 0.78, 95% confidence interval (CI)?= 0.68-0.88]. In the stratified analysis, we found that this protective effect of rs1884444 G allele was mainly evident in intestinal-type gastric cancer (adjusted allelic OR = 0.75, 95% CI = 0.65-0.87) other than in diffuse-type gastric cancer (adjusted allelic OR = 0.96, 95% CI = 0.76-1.22). However, we did not find any significant association of rs6682925 T>C with gastric cancer risk. These findings indicate, for the first time, that the nonsynonymous variant rs1884444 T>G of IL-23R may contribute to gastric cancer susceptibility, especially in intestinal-type gastric cancer, in Chinese population.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1098-2744
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pubmed:author |
pubmed-author:ChenJianjianJ,
pubmed-author:DengBinB,
pubmed-author:DingYanbingY,
pubmed-author:HuZhibinZ,
pubmed-author:HuaZhaolaiZ,
pubmed-author:JinGuangfuG,
pubmed-author:RenChuanliC,
pubmed-author:ShenHongbingH,
pubmed-author:WinSS,
pubmed-author:XuYaochuY,
pubmed-author:ZhangHanzeH,
pubmed-author:ZhouYanY
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pubmed:copyrightInfo |
© 2010 Wiley-Liss, Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
862-8
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pubmed:meshHeading |
pubmed-meshheading:20607725-Asian Continental Ancestry Group,
pubmed-meshheading:20607725-Case-Control Studies,
pubmed-meshheading:20607725-Female,
pubmed-meshheading:20607725-Humans,
pubmed-meshheading:20607725-Male,
pubmed-meshheading:20607725-Middle Aged,
pubmed-meshheading:20607725-Polymorphism, Single Nucleotide,
pubmed-meshheading:20607725-Receptors, Interleukin,
pubmed-meshheading:20607725-Risk,
pubmed-meshheading:20607725-Stomach Neoplasms
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pubmed:year |
2010
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pubmed:articleTitle |
A nonsynonymous polymorphism in IL23R gene is associated with risk of gastric cancer in a Chinese population.
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pubmed:affiliation |
Department of Epidemiology and Biostatistics, Cancer Center, Nanjing Medical University, Nanjing, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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