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钱云, 徐耀初, 沈洪兵, 覃玉, 周玲, 喻荣彬, 钮菊英. 谷胱甘肽转硫酶M1、T1基因多态性与胃癌遗传易感性关系的分子流行病学研究[J]. 中国公共卫生, 2001, 17(2): 101-103. DOI: 10.11847/zgggws2001-17-02-03
引用本文: 钱云, 徐耀初, 沈洪兵, 覃玉, 周玲, 喻荣彬, 钮菊英. 谷胱甘肽转硫酶M1、T1基因多态性与胃癌遗传易感性关系的分子流行病学研究[J]. 中国公共卫生, 2001, 17(2): 101-103. DOI: 10.11847/zgggws2001-17-02-03
QIAN Yun, . A Molecular Epidemiological Study on the Relationship between Glutathione S-Transferase M1, T1 Genetic Polymorphism and Susceptibility to Gastric Cancer[J]. Chinese Journal of Public Health, 2001, 17(2): 101-103. DOI: 10.11847/zgggws2001-17-02-03
Citation: QIAN Yun, . A Molecular Epidemiological Study on the Relationship between Glutathione S-Transferase M1, T1 Genetic Polymorphism and Susceptibility to Gastric Cancer[J]. Chinese Journal of Public Health, 2001, 17(2): 101-103. DOI: 10.11847/zgggws2001-17-02-03

谷胱甘肽转硫酶M1、T1基因多态性与胃癌遗传易感性关系的分子流行病学研究

A Molecular Epidemiological Study on the Relationship between Glutathione S-Transferase M1, T1 Genetic Polymorphism and Susceptibility to Gastric Cancer

  • 摘要: 目的探讨谷胱甘肽转硫酶M1(GSTM1)、T1(GSTT1)基因多态性与胃癌遗传易感性的关系.方法采用病例对照分子流行病学研究方法和聚合酶链反应技术,检测89例原发性胃癌病例和94例对照GSTM1和GSTT1基因型.结果胃癌病例组GSTM1基因缺失频率为61.8%,显着高于对照组(46.8%)(χ2=4.14,P=0.042,OR=1.84,95%CI=1.02~3.31);GSTT1基因缺失频率在病例组为57.3%,也高于对照组48.9%,但未达到统计学显着性水平(χ2=1.28,P=0.257,OR=1.40,95%CI=0.78~2.51).携带GSTM1(-)和GSTT1(+)基因型者发生胃癌的危险性显着高于GSTM1(+)和GSTT1(+)基因型携带者(OR=2.27,95%CI=1.06~4.85).GSTM1基因缺失的吸烟者患胃癌的危险性显着增高(OR=3.09,95%CI=1.33~7.19).结论提示GSTM1空白基因型可能与胃癌易感性有关,GSTMl和GSITl均为空白基因型的个体对胃癌易感性明显增加,GSTM1基因缺失与吸烟在胃癌的发生发展过程中具有协同作用.

     

    Abstract: ObjectiveIn o rder to examine the relationship between glutathiones-transferase M1,T1(GSTM1,GSTT1)genetic polymorphism and susceptibility to gastric cancer.MethodsA case-control study was carried out and polymerase chain reaction (PCR)technique was used to identify GSTM1,GSTT1 genoty pe in 89 cases of primary gastric cancer and 94 controls.ResultsThe frequency of GSTM1 null genotype in patients with gastric cancer(61.8%)showed a statistically significant increase compared to the control group frequency(46.8%)(χ2=4.14,P=0.042, OR=1.84,95% CI=1.02~3.31);the frequency of GSTT1 null genotype in cased(57.3%)was also higher than it in controls, but this increase did not reach statistical sig nificance(χ2=1.28,P=0.257,OR=1.40,95% CI=0.78~2.51);the risk for gastric cancer in those with GSTM1 nun and GSTT1 null genoty pe was significantly higher than that in those with GSTM1 non-null and GSTT1 non-null genotype,with the OR of 2.27 and 95% CI of ORs 1.06~4.85;the risk for gastric cancer in those smoking with GSTM1 null genot ype increased significantly(OR=3.09,95% CI=1.33~7.19).ConclusionGSTM1 null genotype is associated with the risk for gastric cancer;the individuals with GST M1(-)and GSTT1(-)are more susceptibility to gastric cancer;GSTM1 and smoke may cooperate with each other in the occurrence and development of gastric cancer.

     

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