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COX-2 多态性 -765G→C 和 -1195A→G 与肝细胞癌风险。

COX-2 polymorphisms -765G→C and -1195A→G and hepatocellular carcinoma risk.

机构信息

Department of Biochemistry, Faculty of Medicine, Zagazig University, Zagazig, Egypt.

Department of Biochemistry, Faculty of Medicine, Zagazig University, Zagazig, Egypt; Department of Biochemistry, Faculty of Medicine, Taif University, Al Taif, Saudi Arabia.

出版信息

Gene. 2014 Jun 15;543(2):234-6. doi: 10.1016/j.gene.2014.04.014. Epub 2014 Apr 8.

Abstract

Cyclooxygenase-2 (COX-2) is overexpressed in hepatocellular carcinoma (HCC) and considered to play a role in hepatic carcinogenesis. Our aim was to examine the associations between polymorphisms in COX-2 -765G→C and -1195A→G and risk of HCC. We conducted a case-control study including 120 patients with HCC and 130 age- and gender-matched controls. Genotypes of the COX-2 polymorphisms -765G→C and -1195A→G were determined by polymerase chain reaction-based restriction fragment length polymorphism. No significant difference was observed in the genotype distribution of the -765G→C polymorphism between patients and controls. The -1195AA genotype was associated with an increased risk of developing HCC (OR, 2.5; 95%CI, 1.18-5.37). The A allele was present significantly more often in HCC patients (OR 1.5; 95%CI, 1.05-2.14). In conclusion, our results demonstrated that the -1195AA genotype and A allele have an important role in HCC risk in Egyptian patients.

摘要

环氧化酶-2(COX-2)在肝细胞癌(HCC)中过表达,被认为在肝致癌作用中发挥作用。我们的目的是研究 COX-2-765G→C 和-1195A→G 多态性与 HCC 风险之间的关联。我们进行了一项病例对照研究,包括 120 例 HCC 患者和 130 名年龄和性别匹配的对照。通过聚合酶链反应 - 基于限制片段长度多态性确定 COX-2 多态性-765G→C 和-1195A→G 的基因型。在患者和对照组之间,-765G→C 多态性的基因型分布没有观察到显著差异。-1195AA 基因型与 HCC 发病风险增加相关(OR,2.5;95%CI,1.18-5.37)。A 等位基因在 HCC 患者中存在明显更多(OR 1.5;95%CI,1.05-2.14)。总之,我们的结果表明,-1195AA 基因型和 A 等位基因在埃及患者的 HCC 风险中具有重要作用。

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