首页> 美国卫生研究院文献>American Journal of Epidemiology >Genotype Misclassification in Genetic Association Studies of the rs1042522 TP53 (Arg72Pro) Polymorphism: A Systematic Review of Studies of Breast Lung Colorectal Ovarian and Endometrial Cancer
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Genotype Misclassification in Genetic Association Studies of the rs1042522 TP53 (Arg72Pro) Polymorphism: A Systematic Review of Studies of Breast Lung Colorectal Ovarian and Endometrial Cancer

机译:rs1042522 TP53(Arg72Pro)多态性的遗传关联研究中的基因型错误分类:对乳腺癌肺癌结直肠癌卵巢癌和子宫内膜癌研究的系统评价

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摘要

Preferential loss of heterozygosity at the rs1042522 locus of the tumor protein 53 gene (TP53) (Arg72Pro) is observed in several tumors. Genetic association studies in oncology often use tumor tissue rather than unaffected tissue for genotyping; in such cases, loss of heterozygosity at the TP53 locus could lead to differential misclassification and could bias estimates of association. We searched multiple databases (through March 8, 2011) for studies investigating the association of Arg72Pro with breast, lung, colorectal, ovarian, or endometrial cancer. Meta-analysis was performed with multilevel Bayesian models. Informative priors for the bias effect were derived from a meta-analysis of the same polymorphism in cervical cancer. Of 160 studies (68 breast, 42 lung, 26 colorectal, 16 ovarian, and 8 endometrial cancer), 22 used tumor tissue as the source of genotyping material for cases. Use of tumor tissue versus other sources of genotyping material was associated with an apparent protective effect of the proline allele (relative odds ratio = 0.78, 95% credible interval: 0.70, 0.88). The probability that use of tumor tissue induced bias was estimated to be higher than 99%. Use of tumor tissue as the source of genotyping material for cases is associated with significant bias in the estimate of the genetic effect in cancer genetic association studies.
机译:在一些肿瘤中观察到在肿瘤蛋白53基因(TP53)(Arg72Pro)的rs1042522基因座处杂合性的优先损失。肿瘤学中的遗传关联研究通常使用肿瘤组织而不是未受影响的组织进行基因分型。在这种情况下,TP53位点杂合性的丧失可能导致差异分类错误,并可能使关联估计偏倚。我们搜索了多个数据库(截止到2011年3月8日),以研究Arg72Pro与乳腺癌,肺癌,结直肠癌,卵巢癌或子宫内膜癌的相关性。使用多级贝叶斯模型进行荟萃分析。偏倚效应的信息先验来自对子宫颈癌中相同多态性的荟萃分析。在160项研究(68例乳腺癌,42例肺癌,26例结直肠癌,16例卵巢癌和8例子宫内膜癌)中,有22例使用肿瘤组织作为病例的基因分型材料。与其他基因分型材料来源相比,使用肿瘤组织与脯氨酸等位基因具有明显的保护作用(相对优势比= 0.78,95%可信区间:0.70,0.88)。估计使用肿瘤组织引起的偏倚的可能性高于99%。使用肿瘤组织作为病例的基因分型材料的来源与癌症遗传关联研究中遗传效应的估计存在重大偏差。

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