Liu Lei, Jiao Jinghua, Wang Yu, Zhang Dong, Wu Jingyang, Huang Desheng
Department of Ophthalmology, The First Affiliated Hospital, China Medical University, Shenyang City, Liaoning Province, China; Department of Epidemiology, School of Public Health, China Medical University, Shenyang City, Liaoning Province, China.
Department of Anesthesiology, Fengtian Hospital, Shenyang Medical College, Shenyang City, Liaoning Province, China.
PLoS One. 2014 Mar 6;9(3):e90931. doi: 10.1371/journal.pone.0090931. eCollection 2014.
The TP53BP1 gene may be involved in the development of cancer through disrupting DNA repair. However, studies investigating the relationship between TP53BP1 Glu353Asp (rs560191) polymorphism and cancer yielded contradictory and inconclusive outcomes. In order to realize these ambiguous findings, a meta-analysis was performed to assess the association between the TP53BP1 Glu353Asp (rs560191) polymorphism and susceptibility to cancer.
We conducted a search of all English reports on studies for the association between the TP53BP1 Asp353Glu (rs560191) polymorphism and susceptibility to cancer using Medline, the Cochrane Library, EMbase, Web of Science, Google (scholar), and all Chinese reports were identified manually and on-line using CBMDisc, Chongqing VIP database, and CNKI database. The strict selection criteria and exclusion criteria were determined, and odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of associations. The fixed or random effect model was selected based on the heterogeneity test among studies. Publication bias was estimated using funnel plots and Egger's regression test.
A total of seven studies were included in the meta-analysis including 3,213 cases and 3,849 controls. The results indicated that the Glu353Asp (rs560191) polymorphism in TP53BP1 gene had no association with cancer risk for all genetic models. In the subgroup analysis, the results suggested that Glu353Asp polymorphism was not associated with the risk of cancer according to ethnicity, cancer type, genotyping method, adjusted with control or not, HWE and quality score.
This meta-analysis suggested that the Glu353Asp (rs560191) polymorphism in TP53BP1 gene was not associated with risk of cancer.
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基因Glu353Asp(rs560191)多态性与癌症之间关系的研究结果相互矛盾且尚无定论。为了明确这些模糊的研究结果,我们进行了一项荟萃分析,以评估TP53BP1基因Glu353Asp(rs560191)多态性与癌症易感性之间的关联。
我们使用Medline、Cochrane图书馆、EMbase、科学网、谷歌学术搜索了所有关于TP53BP1基因Asp353Glu(rs560191)多态性与癌症易感性关联研究的英文报告,并通过CBMDisc、重庆维普数据库和中国知网数据库手动及在线检索了所有中文报告。确定了严格的纳入标准和排除标准,并使用比值比(OR)及其95%置信区间(CI)评估关联强度。根据各研究间的异质性检验结果选择固定效应模型或随机效应模型。采用漏斗图和Egger回归检验评估发表偏倚。
荟萃分析共纳入7项研究,包括3213例病例和3849例对照。结果表明,TP53BP1基因的Glu353Asp(rs560191)多态性与所有遗传模型下的癌症风险均无关联。亚组分析结果显示,根据种族、癌症类型、基因分型方法、是否调整对照、哈迪-温伯格平衡(HWE)和质量评分,Glu353Asp多态性与癌症风险均无关联。
这项荟萃分析表明,TP53BP1基因的Glu353Asp(rs560191)多态性与癌症风险无关。