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miRNA-146a rs2910164 C>G polymorphism increased the risk of esophagogastric junction adenocarcinoma: a case–control study involving 2,740 participants

机译:miRNA-146a rs2910164 C> G多态性增加食管胃交界处腺癌的风险:一项病例对照研究,涉及2,740名参与者

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Purpose: The miRNA-146a rs2910164 C>G polymorphism may contribute to the development of cancer. However, the association between this polymorphism and the risk of esophagogastric junction adenocarcinoma (EGJA) remains unclear. In the present study, we carried out a case–control study to explore the potential relationship between miRNA-146a rs2910164 C>G polymorphism and EGJA risk. Patients and methods: In total, 1,063 EGJA patients and 1,677 cancer-free controls were enrolled. The SNPscan? genotyping assay, a patented technology, was used to test the genotyping of miRNA-146a rs2910164 C>G polymorphism. Results: We found that miRNA-146a rs2910164 C>G polymorphism was associated with a risk of developing EGJA (additive model: adjusted odds ratio (OR), 1.27; 95% CI, 1.07–1.51; P =0.006; homozygote model: adjusted OR, 1.31; 95% CI, 1.03–1.65; P =0.027 and dominant model: adjusted OR, 1.36; 95% CI, 1.15–1.60; P G polymorphism increased the risk of EGJA in males, females, G polymorphism increased the risk of EGJA in eastern Chinese Han population.
机译:目的:miRNA-146a rs2910164 C> G多态性可能有助于癌症的发展。然而,这种多态性与食管胃交界处腺癌(EGJA)的风险之间的关联仍不清楚。在本研究中,我们进行了病例对照研究,以探讨miRNA-146a rs2910164 C> G多态性与EGJA风险之间的潜在关系。患者和方法:总共纳入了1,063名EGJA患者和1,677名无癌对照。 SNPscan?基因分型分析是一项专利技术,用于测试miRNA-146a rs2910164 C> G多态性的基因分型。结果:我们发现miRNA-146a rs2910164 C> G多态性与罹患EGJA的风险有关(加成模型:调整后的优势比(OR)为1.27; 95%CI为1.07-1.51; P = 0.006;纯合子模式:经过调整OR,1.31; 95%CI,1.03-1.65; P = 0.027和优势模型:校正后OR,1.36; 95%CI,1.15-1.60; PG多态性增加了男性,女性的EGJA风险,G多态性增加了EGJA的风险。 EGJA在中国东部汉族人口中。

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