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Application of Microarray-Based Method for Functional SNP Genotyping in the Risk of Gastric Carcinoma in Chinese Population

机译:微阵列为基础方法在中国人群中胃癌风险中的功能性SNP基因分型

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High-throughput SNP detection microarrays were used here to explore the relationship between 5, 10-methylenetetrahydrofolate reductase (MTHFR) gene polymorphism C677T and the risk of gastric carcinoma among population in Jiangsu region, by genotyping the specimens from 170 patients with gastric carcinoma and 140 age- and sex-matched control subjects. PCR products were spotted onto a 3-aminopropyltriethoxysilane coated glass slide to fabricate a microarray, then interrogated by hybridization with dual-color probes (Cy3, Cy5) to determine the SNP genotype of each sample, and the relation between the genotypes and the risk of gastric carcinoma was analyzed. The frequencies of C677T genotype were CC(47.9%), CT(40%), CT(12.1%) in control group and CC(35.9%), CT(45.9%), TT(18.2%) in gastric carcinoma group, respectively. The individuals with 677CT+TT genotype group or 677TT had a 1.67-fold (95% CI: 1.06-2.64) or 2.67-fold (95% CI: 1.382-5.341) increased risk to develop gastric carcinoma compared with those having 677CC genotype. It was shown that the single nucleotide polymorphisms in the MTHFR gene are associated with the risk of gastric carcinoma in the Chinese population.
机译:高通量SNP检测微阵列这里用来探索5之间10甲基四氢叶酸还原酶(MTHFR)基因多态性C677T和胃癌的江苏区域人口中的风险的关系,通过基因分型从170例患者标本胃癌和140年龄和性别匹配的对照组。 PCR产物点样到3-氨基丙基涂覆的玻璃载片来制作微阵列,然后通过杂交询问与双色探针(CY3,Cy5的)来确定每个样品的SNP的基因型,和基因型和风险之间的关系胃癌进行分析。 C677T的基因型的频率分别在胃癌组CC(47.9%),CT(40%),CT(12.1%)对照组和CC(35.9%),CT(45.9%),TT(18.2%), 。与677CT + TT基因型组或677TT个体有1.67倍(95%CI:1.06-2.64)或2.67倍(95%CI:1.382-5.341)的风险增加与那些具有基因型677CC相比开发胃癌。结果表明,在MTHFR基因的单核苷酸多态性与胃癌在中国人群中的风险有关。

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