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胃肠道恶性肿瘤髓过氧化物酶基因多态性及其活力的相关性研究

A Study on Polymorphism of Myeloperoxidase Gene of Gastrointestinal Cancer and Its Correlation with the Activity
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摘要 目的:了解胃肠道肿瘤患者血液白细胞髓过氧化物酶(myeloperoxidase MPO)基因的多态性及血清酶活力,分析其与胃肠道肿瘤发生的关系。方法:100例胃肠道恶性肿瘤为病例组,100例健康体检者为对照组,采集两组人群静脉血,采用等位基因特异性引物PCR(ASP-PCR)方法检测MPO-463 G/A位点的多态性,紫外分光光度法检测MPO活力。结果:恶性肿瘤组MPO-463G/A位点GG、GA和AA基因型分布频率为70%(70/100)、20%(20/100)和10%(10/100),对照组为58%(58/100)、36%(36/100)和6%(6/100),两组比较差异有统计学意义(χ2=6.03,P<0.05);肿瘤组与对照组MPO酶活力比较差异有统计学意义(F=0.76,P<0.05);MPO-463G/A位点基因GA+AA与GG基因型个体MPO酶活力比较,差异有统计学意义(F值分别为0815,0.7625,P<0.05)。结论:MPO基因463G/A位点多态性与胃肠道恶性肿瘤的发病风险有关;不同MPO基因型导致酶活力改变,此改变可能受MPO-463G/A多态性的影响。 Objective: To understand myeloperoxidase (MPO) gene polymorphism and its activity in patients with gastrointestinal cancer, and to analyze the relationship between MPO and the occurrence of gastrointestinal tumors. Methods: One hundred cases with gastrointestinal tumor and 100 healthy persons served as cancer group and control group respectively. Venous blood was collected. Allele-specific primer PCR (ASP-PCR) method was used for detection of polymorphism of MPO-463G/A locus. MPO activity was examined with UV speetrophotometry. Results: The frequencies of GG, GA and AA genotypes of MP0-463 were 70% (70/100), 20% (20/100) and 10% (10/!00) in cancer group and were 58% (58/100), 36% (36/100) and 6% (6/100) in control group respectively. The difference between the two groups was statistically significant (x^2 = 6.03, P 〈 0.05 ). The difference of MPO activities between cancer group and control group was statistically significant ( F = 0. 76, P 〈 0.05 ). The differences of MPO activities between genotypes GA + AA and GG were statistically significant (F = 0815, 0. 7625, P 〈 0.05 ). Conclusions: MPO463G/A gene polymorphism relates to gastrointestinal cancer and different MPO genotype may lead to activity change which may be influenced by MPO463G/A gene polymorphism.
出处 《贵阳医学院学报》 CAS 2013年第2期152-154,158,共4页 Journal of Guiyang Medical College
关键词 胃肠系统 肿瘤 髓过氧化物酶 基因多态性 gastrointestinal system neoplasms myeloperoxidase gene polymorphism
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