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一项 hOGG1 Ser326Cys 多态性与食管鳞癌风险关联的荟萃分析。

A meta-analysis of the association between the hOGG1 Ser326Cys polymorphism and the risk of esophageal squamous cell carcinoma.

机构信息

College of Life Science, Northwest A & F University, Yangling, Shaanxi, China.

出版信息

PLoS One. 2013 Jun 6;8(6):e65742. doi: 10.1371/journal.pone.0065742. Print 2013.

Abstract

BACKGROUND

Genetic polymorphism of human 8-oxoguanine glycosylase 1 (hOGG1) Ser326Cys (rs1052133) has been implicated in the risk of Esophageal Squamous Cell Carcinoma (ESCC). However, the published findings are inconsistent. We therefore performed a meta-analysis to derive a more precise estimation of the association between the hOGG1 Ser326Cys polymorphism and ESCC risk.

METHODOLOGY/PRINCIPAL FINDINGS: A comprehensive search was conducted to identify eligible studies of hOGG1 Ser326Cys polymorphism and the risk of the ESCC. Three English and two Chinese databases were used, and ten published case-control studies, including 1987 cases and 2926 controls were identified. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the strength of the association in the dominant and recessive model. Pearson correlation coefficient (PCC) and standard error (SE) were used to assess the number of Cys allele and ESCC risk in the additive model. Overall, significant associations between the hOGG1 Ser326Cys polymorphism and ESCC risk were found in the recessive model: OR = 1.37 (95% CI: 1.06-1.76, p = 0.02). We also observed significant associations in the Caucasian, Chinese language, population based control and tissue subgroups. In the additive model, positive correlation was found between the number of Cys allele and the risk of ESCC in overall studies (PCC = 0.109, SE = 0.046, p = 0.02), Caucasian subgroup and population subgroup. Funnel plot and Egger's test indicate there was no publication bias in this meta-analysis.

CONCLUSION

Under the published data, the hOGG1 Ser326Cys polymorphism is associated with ESCC risk in the recessive and additive model. Compared with the Ser/Ser and Ser/Cys genotype, Cys/Cys genotype might contribute to increased risk of ESCC. And the risk of ESCC is positively correlated with the number of Cys allele. A better case-control matched study should be designed in order to provide a more precise estimation.

摘要

背景

人类 8-氧鸟嘌呤糖苷酶 1(hOGG1)Ser326Cys(rs1052133)的遗传多态性与食管鳞状细胞癌(ESCC)的风险有关。然而,已发表的研究结果并不一致。因此,我们进行了荟萃分析,以更准确地评估 hOGG1 Ser326Cys 多态性与 ESCC 风险之间的关联。

方法/主要发现:我们全面检索了有关 hOGG1 Ser326Cys 多态性与 ESCC 风险的研究,使用了三个英文数据库和两个中文数据库,共鉴定出 10 项符合条件的病例对照研究,包括 1987 例病例和 2926 例对照。我们使用优势比(ORs)和 95%置信区间(CIs)评估显性和隐性模型中的关联强度。使用 Pearson 相关系数(PCC)和标准误差(SE)评估加性模型中 Cys 等位基因的数量与 ESCC 风险之间的关系。总体而言,在隐性模型中,hOGG1 Ser326Cys 多态性与 ESCC 风险之间存在显著关联:OR=1.37(95%CI:1.06-1.76,p=0.02)。我们还观察到在高加索人、中文语言、基于人群的对照和组织亚组中存在显著关联。在加性模型中,总体研究(PCC=0.109,SE=0.046,p=0.02)、高加索人亚组和人群亚组中均发现 Cys 等位基因数量与 ESCC 风险之间存在正相关。漏斗图和 Egger 检验表明,该荟萃分析不存在发表偏倚。

结论

根据已发表的数据,hOGG1 Ser326Cys 多态性与 ESCC 风险在隐性和加性模型中相关。与 Ser/Ser 和 Ser/Cys 基因型相比,Cys/Cys 基因型可能会增加 ESCC 的风险。并且 ESCC 的风险与 Cys 等位基因的数量呈正相关。应该设计更好的病例对照匹配研究,以提供更准确的估计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d4/3675068/b0b72667a7e3/pone.0065742.g001.jpg

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