Abstract
沈靖,王润田,王理伟,王朝曦,邢厚恂,王滨燕,李茂森,华召来,王建明,郭春华,王心如,徐希平.胃癌易感性与诱导型一氧化氮合酶基因多态性关系的研究[J].Chinese journal of Epidemiology,2002,23(5):374-377
胃癌易感性与诱导型一氧化氮合酶基因多态性关系的研究
Study on the Relationship between susceptibility of stomach neoplasm cancer and polymorphism of inducible Nitric Oxide Synthase gene
Received:February 01, 2002  
DOI:
KeyWord: 一氧化氮合酶  基因  多态性  胃肿瘤
English Key Word: Nitricoxides  ynthase  gene  Polymorphism Stomach neoplasms
FundProject:国家自然科学基金资助项目 (30170827和30070671)
Author NameAffiliation
SHEN Jing 210029 南京医科大学公共卫生学院流行病与卫生统计学系 
WANG Runtian 210029 南京医科大学公共卫生学院流行病与卫生统计学系 
WANG Liwei 210029 南京医科大学公共卫生学院流行病与卫生统计学系 
WANG Zhaoxi 北京大学公共卫生学院流行病与卫生统计学系 
XING Houxun 江苏省扬中市肿瘤防治研究所流行病室 
WANG Binyan 江苏省扬中市肿瘤防治研究所流行病室 
LI Maosen 江苏省扬中市肿瘤防治研究所流行病室 
HUA Zhaolai 江苏省扬中市肿瘤防治研究所流行病室 
WANG Jianming 江苏省扬中市肿瘤防治研究所流行病室 
GUO Chunhua 北京大学生态遗传与生殖卫生研究中心 
WANG Xinru 北京大学生态遗传与生殖卫生研究中心 
XU Xiping 安徽医科大学生物医学研究所 
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Abstract:
      目的探讨中国人诱导型一氧化氮合酶(iNOS)基因多态性与胃癌易感性的关系。方法以社区为基础的病例对照研究。病例经胃镜及病理确诊,有效分析样本包括肠型胃癌93例,胃贲门癌50例,对照246人。结果iNOS基因第16外显子存在C→T多态性(产生Tsp509Ⅰ内切酶的识别位点),使编码的氨基酸由丝氨酸(Ser)改变为亮氨酸(Leu),对照人群T等位基因频率为13.21%,单独存在C→T多态性与肠型胃癌、胃贲门癌易感性增加无统计学关联,但与吸烟因素同时存在,对肠型胃癌、胃贲门癌产生明显的2型超相乘交互作用;与缺乏CagA抗体同时存在,对胃贲门癌产生明显的相加交互作用。结论iNOS基因C→T多态性可能是胃癌的易感基因,特别与吸烟、缺乏幽门螺杆菌CagA抗体的肠型胃癌、胃贲门癌发生密切相关。
English Abstract:
      Objective To study the relationship between polymorphism of inducible Nitric Oxide Synthase (iNOS) gene and the susceptibility of intestinal type stomach cancer and stomach cardia cancer in Chinese people. Methods A community based case control study was designed. Ninety three intestinal type of stomach cancer and 50 stomach cardia cancer patients with endoscopy and pathology diagnosis were identified as cases. Two hundred and forty six controls served as controls.Results C→T polymorphism was found in exon 16 of iNOS gene, which changed the coding amino acid from serine to leucine, and formed a recognition site identified by Tsp 509Ⅰ restriction enzyme (we called it C→T polymorphism). The T allele gene frequency in the control group was 13.21 %. No statistically significant difference was found between C→T polymorphism alone and the increased susceptibility to intestinal stomach cancer or stomach cardia cancer. A significant type 2 multiplicative interaction was found in increasing both the risk of intestinal stomach cancer and stomach cardia cancer when both C→T polymorphism and tobacco smoking exposure existed. An additive interaction model, which showed statistically significant difference, was found to increase only the risk of stomach cardia cancer when CagA antibody shared negative but C→T polymorphism occurred. Conclusion C→T polymorphism of iNOS gene was considered as one of the possible susceptible genes, which specifically increased the risk of tobacco related but CagA negative types of intestinal stomach cancer and stomach cardia cancer.
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