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G870A基因多态性与食管癌易感性:一项荟萃分析。

Genetic polymorphism of G870A and esophageal cancer susceptibility: A meta-analysis.

作者信息

He Wenwu, Zeng Yanbei, Long Jianxiong, Zhou Qiuxi, Hu Yanling, Chen Mingwu

机构信息

Department of Cardiothoracic Surgery, Guangxi Medical University, Nanning, Guangxi, P.R. China ;

Clinical Medicine Major, First Affiliated Hospital, Guangxi Medical University, Nanning, Guangxi, P.R. China ;

出版信息

Biomed Rep. 2013 Mar;1(2):303-307. doi: 10.3892/br.2012.50. Epub 2012 Dec 20.

Abstract

The association between the polymorphism of cyclin D1 () and esophageal carcinogenicity has been widely examined, however, it remains controversial. To evaluate the importance of G870A polymorphism with regard to the risk of esophageal cancer, a meta-analysis was carried out that reviewed the available literature in order to clarify the controversies. This meta-analysis included 1,154 cases and 1,678 controls for G870A polymorphism from seven published case-control studies. The odds ratio (OR) and 95% confidence interval (CI) were calculated using the Stata software version 11.1. The results were pooled using a dominant model to appropriately reflect a biological model of the genetic effect. No significant association was observed in the Caucasian (OR=1.64; 95% CI, 0.84-3.20) or the Asian populations (OR=1.30; 95% CI, 0.65-2.62), while no significant association was found in esophageal squamous cell carcinoma (ESCC) (OR=1.74; 95% CI, 0.79-3.81) or esophageal adenocarcinoma (EADC) (OR=1.18; 95% CI, 0.77-1.81). However, the comparison of A vs. G in G870A showed significant differential susceptibility to esophageal cancer (OR=1.26; 95% CI, 1.00-1.59). These findings suggested that the G870A polymorphism has no association with esophageal cancer risk in ethnicity and histology, respectively. Further studies are required to assess these associations in greater detail.

摘要

细胞周期蛋白D1()的多态性与食管癌致癌性之间的关联已得到广泛研究,然而,仍存在争议。为了评估G870A多态性对食管癌风险的重要性,进行了一项荟萃分析,该分析回顾了现有文献以澄清争议。这项荟萃分析纳入了来自七项已发表的病例对照研究的1154例病例和1678例对照,用于G870A多态性研究。使用Stata软件11.1版计算比值比(OR)和95%置信区间(CI)。结果采用显性模型进行汇总,以适当反映遗传效应的生物学模型。在白种人(OR = 1.64;95% CI,0.84 - 3.20)或亚洲人群(OR = 1.30;95% CI,0.65 - 2.62)中未观察到显著关联,在食管鳞状细胞癌(ESCC)(OR = 1.74;95% CI,0.79 - 3.81)或食管腺癌(EADC)(OR = 1.18;95% CI,0.77 - 1.81)中也未发现显著关联。然而,G870A中A与G的比较显示对食管癌存在显著的易感性差异(OR = 1.26;95% CI,1.00 - 1.59)。这些发现表明,G870A多态性分别与种族和组织学类型的食管癌风险无关。需要进一步研究以更详细地评估这些关联。

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