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p53密码子72多态性与宫颈肿瘤:一项荟萃分析综述

p53 codon 72 polymorphism and cervical neoplasia: a meta-analysis review.

作者信息

Koushik Anita, Platt Robert W, Franco Eduardo L

机构信息

Department of Epidemiology and Biostatistics, McGill University, Montréal, Québec, Canada.

出版信息

Cancer Epidemiol Biomarkers Prev. 2004 Jan;13(1):11-22. doi: 10.1158/1055-9965.epi-083-3.

Abstract

The Arg/Arg genotype versus Arg/Pro or Pro/Pro at codon 72 of the p53 gene has been implicated as a risk marker in cervical neoplasia. However, research on this topic has produced controversial results. We reviewed the published literature to summarize the association and to identify methodological features that may have contributed to the heterogeneity. Information on specific methodological features of studies addressing this topic published between 1998 and 2002 were obtained. Study-specific odds ratios (ORs) were combined in a meta-analysis, assuming random effects. To identify characteristics that significantly contributed to heterogeneity, we used meta-regression analysis. We identified 50 articles, of which 45 were included in the meta-analyses and regressions. No evidence of association or heterogeneity was detected for preinvasive lesions. For invasive cervical cancer with undefined histology, the Arg/Arg genotype was not found to affect risk (OR, 1.1; 95% confidence interval (CI), 0.9-1.3). However, a slightly increased risk was observed for squamous cell carcinoma (OR, 1.5; 95% CI, 1.2-1.9) and adenocarcinoma (OR, 1.7; 95% CI, 1.0-2.7). Meta-regression analysis identified that the most important factor contributing to heterogeneity among results for invasive lesions was departures from Hardy-Weinberg equilibrium in the control group. Summary ORs for studies in equilibrium were essentially null. A possible susceptibility role by the p53 codon 72 polymorphism at a late carcinogenetic stage in cervical cancer cannot be ruled out. However, various methodological features can contribute to departures from Hardy-Weinberg equilibrium and consequently to less than ideal circumstances for the examination of this polymorphism. Future investigations require appropriate attention to design and methodological issues.

摘要

p53基因第72位密码子处的Arg/Arg基因型与Arg/Pro或Pro/Pro基因型相比,已被认为是宫颈肿瘤形成的一个风险标志物。然而,关于这一主题的研究结果存在争议。我们回顾了已发表的文献,以总结两者之间的关联,并确定可能导致异质性的方法学特征。获取了1998年至2002年间发表的关于该主题研究的具体方法学特征信息。在随机效应模型下,将各研究的特异比值比(OR)进行合并,进行荟萃分析。为了确定对异质性有显著影响的特征,我们采用了荟萃回归分析。我们共筛选出50篇文章,其中45篇纳入了荟萃分析和回归分析。对于癌前病变,未发现关联或异质性的证据。对于组织学类型不明确的浸润性宫颈癌,未发现Arg/Arg基因型会影响风险(OR为1.1;95%置信区间[CI]为0.9 - 1.3)。然而,在鳞状细胞癌(OR为1.5;95% CI为1.2 - 1.9)和腺癌(OR为1.7;95% CI为1.0 - 2.7)中观察到风险略有增加。荟萃回归分析表明,导致浸润性病变结果异质性的最重要因素是对照组偏离了哈迪-温伯格平衡。处于平衡状态的研究的汇总OR基本为零。不能排除p53基因第72位密码子多态性在宫颈癌致癌后期可能具有的易感性作用。然而,各种方法学特征可能导致偏离哈迪-温伯格平衡,从而不利于对这种多态性的检测。未来的研究需要适当关注设计和方法学问题。

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