Polymorphisms in MUC1, MUC2, MUC5B and MUC6 genes are not associated with the risk of chronic atrophic gastritis

被引:8
|
作者
Frank, Bernd [1 ]
Weck, Melanie Nicole [1 ]
Mueller, Heiko [1 ]
Klopp, Norman [2 ]
Illig, Thomas [2 ]
Raum, Elke [1 ]
Brenner, Hermann [1 ]
机构
[1] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, D-69120 Heidelberg, Germany
[2] Res Ctr Environm & Hlth, Inst Epidemiol, Neuherberg, Germany
关键词
Mucins; Polymorphism; Chronic atrophic gastritis; Gastric cancer; Risk; HELICOBACTER-PYLORI INFECTION; PRECANCEROUS PROCESS; OLDER-ADULTS; CANCER; POPULATION; EXPRESSION; CARCINOMA; MUCINS; CARCINOGENESIS; ADENOCARCINOMA;
D O I
10.1016/j.ejca.2011.04.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mucins represent major components of the mucous layer in the stomach, protecting the underlying epithelium from acid, mechanical trauma, proteases and pathogenic bacteria. Previous studies have shown an association of neoplastic transformation in the stomach with aberrant mucin levels, suggesting a potential role of genetic variation in mucin genes in the development of gastric cancer (GC). We assessed the association of genetic variation in candidate single nucleotide polymorphisms (SNPs) in mucin genes with the risk of chronic atrophic gastritis (CAG), a well-established precursor of GC in the German population-based ESTHER study. We genotyped MUC1 T31T, MUC2 L58P, MUC2 V116M, MUC5B E34G, MUC5B R51W, MUC5B rs2014486 (intronic) and MUC6 V619M for 533 serologically defined CAG cases and 1054 age- and sex-matched controls. None of the analysed SNPs was associated with CAG. However, large studies are needed to disclose or exclude potential weak associations of these SNPs with CAG risk. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:114 / 120
页数:7
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