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Study on the association of COX-2 genetic polymorphisms with risk of gastric cancer in high incidence Hexi area of Gansu province in China

机译:甘肃河西高发区COX-2基因多态性与胃癌危险性的关系研究

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摘要

To investigate the possible association of polymorphisms, cyclooxygenase-2 (COX-2) promoter region 899G>C, COX-2 codon 587G>A, with risk of gastric cancer in the high incidence Hexi area of Gansu province in China. Blood samples from 140 patients with gastric carcinoma and 125 normal persons were collected in Hexi area of Gansu province in China. Polymorphisms of COX-2 899G>A and COX-2 587G>A were genotyped by PCR-TaqMan. For detection Helicobacter pylori infection, Warhin-Starry staining was used. Three kinds of polymorphisms of COX-2 899G>C were GG, GC and CC. The frequencies in gastric cancer patients were 72.9, 21.4 and 5.7%, and the frequencies in controls were 84.0, 12.8 and 3.2%, respectively. COX-2 899C carrier (GC + CC) increased risk of gastric carcinoma with an odds ratio 1.950 (95% CI: 1.067-3.586, P = 0.029). The genotype of COX-2 587G>A polymorphism were GG, GA and AA. The frequencies in patients group were 86.4, 11.4 and 2.2%, and the frequencies in controls were 89.6, 9.6 and 0.8%, respectively. There was no significant difference between cases and controls in each genotype. Helicobacter pylori infection rate was 68.6% in patients group and 50.4% in healthy controls. Helicobacter pylori infection rate in gastric cancer patients was remarkably higher than that in normal people (OR: 2.147, 95% CI: 1.302-3.541, P = 0.003). Stratification analysis was showed that COX-2 899C carrier genotype with Helicobacter pylori infection was significantly higher in cases than that in healthy controls (OR: 4.000, 95% CI: 1.638-9.770). The polymorphism of COX-2 899G>C could be a risk factor for gastric cancer in high incidence Hexi area of Gansu Province in China. COX-2 899C carrier genotype and Helicobacter pylori positive infection may have a synergistic effect on gastric cancer in high incidence Hexi area of Gansu Province in China. However, the polymorphisms of COX-2 587G>A is no association with gastric cancer in the high incidence Hexi area of Gansu Province in China.
机译:目的探讨中国甘肃河西高发地区环加氧酶2(COX-2)启动子区域899G> C,COX-2密码子587G> A与胃癌风险的可能相关性。在中国甘肃河西地区收集了140例胃癌患者和125例正常人的血样。通过PCR-TaqMan对COX-2 899G> A和COX-2 587G> A的多态性进行基因分型。为了检测幽门螺杆菌感染,使用了Warhin-Starry染色。 COX-2 899G> C的三种多态性为GG,GC和CC。胃癌患者的频率分别为72.9、21.4和5.7%,对照组的频率分别为84.0、12.8和3.2%。 COX-2 899C携带者(GC + CC)增加患胃癌的风险,比值比为1.950(95%CI:1.067-3.586,P = 0.029)。 COX-2 587G> A多态性的基因型为GG,GA和AA。患者组的频率分别为86.4%,11.4%和2.2%,对照组的频率分别为89.6%,9.6%和0.8%。每种基因型的病例和对照之间没有显着差异。患者组幽门螺杆菌感染率为68.6%,健康对照组为50.4%。胃癌患者的幽门螺杆菌感染率明显高于正常人(OR:2.147,95%CI:1.302-3.541,P = 0.003)。分层分析表明,感染幽门螺杆菌的COX-2 899C携带者基因型在病例中显着高于健康对照者(OR:4.000,95%CI:1.638-9.770)。 COX-2 899G> C的多态性可能是甘肃河西高发地区胃癌的危险因素。 COX-2 899C携带者基因型和幽门螺杆菌阳性感染可能在中国甘肃河西高发区对胃癌有协同作用。然而,在中国甘肃河西高发地区,COX-2 587G> A的多态性与胃癌无关。

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