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TP53基因多态性与肺癌风险:一项系统评价和荟萃分析。

TP53 polymorphisms and lung cancer risk: a systematic review and meta-analysis.

作者信息

Matakidou A, Eisen T, Houlston R S

机构信息

Section of Cancer Genetics, Institute of Cancer Research, Sutton SM2 5NG, UK.

出版信息

Mutagenesis. 2003 Jul;18(4):377-85. doi: 10.1093/mutage/geg008.

Abstract

To examine the risk of lung cancer associated with the codon 72, intron 6 and intron 3 TP53 polymorphisms a meta-analysis of published case-control studies was undertaken. The principle outcome measure was the odds ratio (OR) for the risk of lung cancer using homozygosity of the 'wild-type allele' as the reference group. Data from 13 studies detailing the relationship between lung cancer and the codon 72 polymorphism of TP53 and three studies examining the intron 3 and 6 polymorphisms of TP53 were analysed. The ORs of lung cancer associated with the Pro-Pro and Pro-carrier genotypes of codon 72 were 1.18 [95% confidence interval (CI) 0.99-1.41] and 1.02 (95% CI 0.86-1.20), respectively. The ORs of lung cancer associated with homozygous and variant allele carrier genotypes of the intron 6 (MspI RFLP) polymorphism were 1.13 (95% CI 0.55-2.27) and 1.30 (95% CI 0.75-2.26) and of the intron 3 (16 bp duplication) polymorphism were 1.50 (95% CI 0.76-2.97) and 1.11 (95% CI 0.53-2.35), respectively. Although polymorphic variations in TP53 represent attractive candidate susceptibility alleles for lung cancer the results from this analysis provide little support for this hypothesis. Additional well-designed studies based on sample sizes commensurate with the detection of small genotypic risks may allow a more definitive conclusion.

摘要

为了研究与密码子72、内含子6和内含子3的TP53基因多态性相关的肺癌风险,我们对已发表的病例对照研究进行了荟萃分析。主要结局指标是以“野生型等位基因”纯合子作为参照组的肺癌风险优势比(OR)。分析了13项详述肺癌与TP53密码子72多态性之间关系的研究数据,以及3项研究TP53内含子3和6多态性的研究数据。与密码子72的Pro-Pro和Pro-携带者基因型相关的肺癌OR分别为1.18 [95%置信区间(CI)0.99 - 1.41]和1.02(95% CI 0.86 - 1.20)。与内含子6(MspI限制性片段长度多态性)多态性的纯合子和变异等位基因携带者基因型相关的肺癌OR分别为1.13(95% CI 0.55 - 2.27)和1.30(95% CI 0.75 - 2.26),与内含子3(16 bp重复)多态性相关的肺癌OR分别为1.50(95% CI 0.76 - 2.97)和1.11(95% CI 0.53 - 2.35)。尽管TP53的多态性变异是肺癌有吸引力的候选易感等位基因,但该分析结果几乎无法支持这一假设。基于与检测小基因型风险相匹配的样本量进行的其他精心设计的研究可能会得出更明确的结论。

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