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TP53BP1基因rs2602141 A/C多态性与癌症风险的关联:一项系统评价和荟萃分析。

Association between the TP53BP1 rs2602141 A/C polymorphism and cancer risk: a systematic review and meta-analysis.

作者信息

Liu Lei, Zhang Dong, Jiao Jing-Hua, Wang Yu, Wu Jing-Yang, Huang De-Sheng

机构信息

Department of Ophthalmology, The First Affiliated Hospital, China Medical University, Shenyang, China E-mail :

出版信息

Asian Pac J Cancer Prev. 2014;15(6):2917-22. doi: 10.7314/apjcp.2014.15.6.2917.

Abstract

BACKGROUND

The p53-binding protein 1 (TP53BP1) gene may be involved in the development of cancer through disrupting DNA repair. However, investigation of associations between TP53BP1 rs2602141 A/C polymorphism and cancer have yielded contradictory and inconclusive outcomes. We therefore performed a meta-analysis to evaluate the association between the TP53BP1 rs2602141 A/C polymorphism and cancer susceptibility.

MATERIALS AND METHODS

Published literature from PubMed, Medline, the Cochrane Library, EMbase, Web of Science, Google (scholar), CBMDisc, Chongqing VIP database, and CNKI database were retrieved. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using fixed or random-effects models. Publication bias was estimated using funnel plots, Begg's and Egger's test.

RESULTS

A total of seven studies (3,018 cases and 5,548 controls) were included in the meta-analysis. Our results showed that the genotype distribution of TP53BP1 rs2602141 A/C was not associated with cancer risk overall. However, on subgroup analysis, we found that TP53BP1 rs2602141 A/C was associated with cancer risk within an allele model (A vs C, OR=1.14, 95%CI: 1.01-1.29) and a codominant model (AA vs CC, OR=1.36, 95%CI: 1.06-1.74) in Asians rather than in Caucasians. Subgroup analysis by cancer type, genotype, and with or without adjustment for controls showed no significant association.

CONCLUSIONS

The findings suggested an association between rs2602141 A/C polymorphism in TP53BP1 gene and increased risk of cancer in Asians.

摘要

背景

p53结合蛋白1(TP53BP1)基因可能通过破坏DNA修复参与癌症的发生发展。然而,关于TP53BP1 rs2602141 A/C多态性与癌症之间关联的研究结果相互矛盾且尚无定论。因此,我们进行了一项荟萃分析,以评估TP53BP1 rs2602141 A/C多态性与癌症易感性之间的关联。

材料与方法

检索了来自PubMed、Medline、Cochrane图书馆、EMbase、科学网、谷歌学术、中国生物医学文献数据库、重庆维普数据库和中国知网数据库的已发表文献。使用固定或随机效应模型计算合并优势比(OR)及95%置信区间(CI)。采用漏斗图、Begg检验和Egger检验评估发表偏倚。

结果

荟萃分析共纳入7项研究(3018例病例和5548例对照)。我们的结果显示,总体上TP53BP1 rs2602141 A/C的基因型分布与癌症风险无关。然而,亚组分析发现,在等位基因模型(A与C,OR = 1.14,95%CI:1.01 - 1.29)和共显性模型(AA与CC,OR = 1.36,95%CI:1.06 - 1.74)中,TP53BP1 rs2602141 A/C与亚洲人的癌症风险相关,而非与高加索人的癌症风险相关。按癌症类型、基因型以及是否对对照进行调整的亚组分析均未显示出显著关联。

结论

研究结果表明TP53BP1基因中的rs2602141 A/C多态性与亚洲人患癌风险增加之间存在关联。

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