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幽门螺杆菌 cag 致病岛的基因多态性与胃癌和高级别癌前胃病变的风险。

Genetic polymorphisms in the cag pathogenicity island of Helicobacter pylori and risk of stomach cancer and high-grade premalignant gastric lesions.

机构信息

Genomic Epidemiology Group, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Department of Translation Research and of New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.

出版信息

Int J Cancer. 2020 Nov 1;147(9):2437-2445. doi: 10.1002/ijc.33032. Epub 2020 May 14.

DOI:10.1002/ijc.33032
PMID:32363734
Abstract

Helicobacter pylori (Hp) infects the stomach of about half of the human population and is strongly associated with the risk of gastric cancer (GC) and its premalignant precursors. The cag pathogenicity island (cagPAI) is a region of the Hp genome encoding for key molecular machinery involved in the infection process. Following a sequencing study, we selected 50 genetic polymorphisms located in seven cagPAI genes and tested their associations with the risk of advanced gastric premalignant lesions and GC in 1220 subjects from various Latin American populations showing the whole spectrum of phenotypes from gastritis to GC. We found that three polymorphisms of cagA are associated with the risk of advanced gastric premalignant lesions (incomplete intestinal metaplasia [ie, Type 2 and 3] or dysplasia), and that six polymorphisms located in cagA, cagL and cagI were associated with risk of GC. When corrected for multiple testing none of the associations were statistically significant. However, scores built by integrating the individual polymorphisms were significantly associated with the risk of advanced gastric premalignant lesions and GC. These results have the potential of establishing markers for risk stratification in the general population, in view of targeting Hp eradication to high-risk population groups.

摘要

幽门螺杆菌(Hp)感染了约一半的人类的胃部,与胃癌(GC)及其癌前病变的风险密切相关。细胞毒素相关基因座(cagPAI)是 Hp 基因组中的一个区域,编码参与感染过程的关键分子机制。在一项测序研究之后,我们选择了位于七个 cagPAI 基因中的 50 个遗传多态性,并在来自不同拉丁美洲人群的 1220 名受试者中测试了它们与晚期胃前癌前病变和 GC 的风险之间的关联,这些受试者表现出从胃炎到 GC 的各种表型。我们发现,cagA 的三个多态性与晚期胃前癌前病变(不完全肠化生[即,类型 2 和 3]或发育不良)的风险相关,而位于 cagA、cagL 和 cagI 中的六个多态性与 GC 的风险相关。在进行多次检验校正后,这些关联均无统计学意义。然而,通过整合个体多态性构建的评分与晚期胃前癌前病变和 GC 的风险显著相关。鉴于针对高危人群组根除 Hp,这些结果有可能确立一般人群的风险分层标志物。

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