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该多态性与胃癌之间关联的研究。

Investigation of the association between the polymorphism and gastric cancer.

作者信息

Tas Ayca, Atabey Mustafa, Caglayan Gulcin, Bostanci Meric Emre, Sahin Bolukbasi Serap, Topcu Omer, Silig Yavuz

机构信息

Department of Nutrition and Diet, Cumhuriyet University, Faculty of Health Sciences, 58140 Sivas, Turkey.

Department of General Surgery, Cumhuriyet University, Faculty of Medicine, 58140 Sivas, Turkey.

出版信息

Biomed Rep. 2017 Nov;7(5):469-473. doi: 10.3892/br.2017.978. Epub 2017 Sep 11.

Abstract

Murine double minute clone 2 oncoprotein (MDM2) is a key component in the regulation of the tumour suppressor p53. The association between the polymorphism and gastric cancer (GC) has been investigated in Turkish population. In the present case-control study, the aim was to investigate the association between genetic polymorphisms of the gene (a major regulator of p53 function) and primary GC risk in a Turkish population. The polymorphism, (rs2279744) in the gene was determined in patients with GC (n=65) and in healthy control subjects (n=67) using the polymerase chain reaction-restriction fragment length polymorphism method. The findings were evaluated using logistic regression and χ tests. No statistically significant differences were observed between the control subjects and patients with GC regarding smoking status. A comparison between GC cases and control subjects indicated a statistically significant difference for family history of cancer [odds ratio (OR)=0.17; 95% confidence interval (CI), 0.05-0.56; χ=0.19; P=0.01]. A significant difference was identified in the GG genotype distribution between GC patients and control subjects (OR=4.58; 95% CI, 1.18-17.79; P=0.022). Thus, the results of the present study indicate that the gene intron (GG) genotype may be an important risk factor for GC development in the Turkish population.

摘要

小鼠双微体克隆2癌蛋白(MDM2)是肿瘤抑制因子p53调控中的关键组成部分。在土耳其人群中,已对该多态性与胃癌(GC)之间的关联进行了研究。在本病例对照研究中,目的是调查该基因(p53功能的主要调节因子)的基因多态性与土耳其人群原发性GC风险之间的关联。采用聚合酶链反应-限制性片段长度多态性方法,对65例GC患者和67例健康对照者的该基因多态性(rs2279744)进行了测定。使用逻辑回归和χ检验对结果进行评估。在吸烟状况方面,对照者与GC患者之间未观察到统计学上的显著差异。GC病例与对照者之间的比较表明,癌症家族史存在统计学上的显著差异[比值比(OR)=0.17;95%置信区间(CI),0.05 - 0.56;χ=0.19;P=0.01]。在GC患者与对照者之间,GG基因型分布存在显著差异(OR=4.58;95% CI,1.18 - 17.79;P=0.022)。因此,本研究结果表明该基因内含子(GG)基因型可能是土耳其人群GC发生的一个重要危险因素。

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