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沙特人群中Arg72Pro p53基因多态性与癌症风险无关联证据:一项荟萃分析。

No Evidence of Association of the Arg72Pro p53 Gene Polymorphism with Cancer Risk in the Saudi Population: a Meta-Analysis.

作者信息

Irshad Mohammad, Mandal Raju Kumar, Al-Drees Abdulmajeed, Khalil Mahmoud Salah, Abdulghani Hamza Mohammad

机构信息

Department of Medical Education, College of Medicine, King Saud University, Riyadh, Saudi Arabia E-mail :

出版信息

Asian Pac J Cancer Prev. 2015;16(14):5663-7. doi: 10.7314/apjcp.2015.16.14.5663.

Abstract

BACKGROUND

Earlier studies on the association between p53 codon 72 Arg>Pro polymorphism and cancer risk were inconclusive and conflicting for the Saudi population. Therefore, we performed a meta-analysis to investigate the relationship between the codon 72 Arg>Pro polymorphism and overall cancer risk in Saudi Arabia.

MATERIALS AND METHODS

We searched all eligible published studies and data were pooled together to perform the meta-analysis. Pooled odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated for homozygous, heterozygous, dominant and recessive genetic models.

RESULTS

A total of five eligible published studies covering 502 cancer cases and 784 healthy controls were included in the meta-analysis. No publication bias was detected in this study. The results suggested that the variant (Pro vs Arg: p=0.960; OR=1.004, 95% CI=0.852-1.183), homozygous (Pro.Pro vs Arg.Arg: p=0.970; OR=1.006, 95% CI=0.729-1.390), heterozygous (Arg.Pro vs Arg.Arg: p=0.473; OR=0.783, 95% CI=0.402-1.527) carriers were not associated with overall cancer risk. Similarly, dominant (Pro.Pro+Pro.Arg vs Arg.Arg: p=0.632; OR=0.886, 95% CI=0.540-1.454) and recessive (Pro.Pro vs Pro.Arg+Arg.Arg: p=0.269; OR=1.163, 95%CI=0.890-1.521) models also did not indicate increased risk of cancer.

CONCLUSIONS

The current meta-analysis suggests that the codon 72 Arg>Pro polymorphism of the p53 gene might not contribute to cancer susceptibility in Saudi population. Future well designed large case control studies are needed to validate our findings.

摘要

背景

先前关于p53基因密码子72位点精氨酸(Arg)>脯氨酸(Pro)多态性与癌症风险之间关联的研究,对于沙特人群而言,结论尚无定论且相互矛盾。因此,我们进行了一项荟萃分析,以探究该密码子72位点Arg>Pro多态性与沙特人群总体癌症风险之间的关系。

材料与方法

我们检索了所有符合条件的已发表研究,并将数据汇总以进行荟萃分析。针对纯合子、杂合子、显性和隐性遗传模型,计算了合并比值比(OR)和95%置信区间(95%CI)。

结果

共有五项符合条件的已发表研究纳入了荟萃分析,涵盖502例癌症病例和784例健康对照。本研究未检测到发表偏倚。结果表明,该变异体(Pro与Arg相比:p = 0.960;OR = 1.004,95%CI = 0.852 - 1.183)、纯合子(Pro.Pro与Arg.Arg相比:p = 0.970;OR = 1.006,95%CI = 0.729 - 1.390)、杂合子(Arg.Pro与Arg.Arg相比:p = 0.473;OR = 0.783,95%CI = 0.402 - 1.527)携带者与总体癌症风险无关。同样,显性模型(Pro.Pro + Pro.Arg与Arg.Arg相比:p = 0.632;OR = 0.886,95%CI = 0.540 - 1.454)和隐性模型(Pro.Pro与Pro.Arg + Arg.Arg相比:p = 0.269;OR = 1.163,95%CI = 0.890 - 1.521)也未表明癌症风险增加。

结论

当前的荟萃分析表明,p53基因密码子72位点的Arg>Pro多态性可能与沙特人群的癌症易感性无关。未来需要设计良好的大型病例对照研究来验证我们的研究结果。

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