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对p53突变数据库中突变型p53生物学活性的荟萃分析揭示了突变检测中的一种方法学偏差。

Meta-analysis of the p53 mutation database for mutant p53 biological activity reveals a methodologic bias in mutation detection.

作者信息

Soussi Thierry, Asselain Bernard, Hamroun Dalil, Kato Shunsuke, Ishioka Chikashi, Claustres Mireille, Béroud Christophe

机构信息

Laboratoire de Génotoxicologie des tumeurs, UPMC, Dpt Pneumologie, Hôpital Tenon, Paris, France.

出版信息

Clin Cancer Res. 2006 Jan 1;12(1):62-9. doi: 10.1158/1078-0432.CCR-05-0413.

Abstract

PURPOSE

Analyses of the pattern of p53 mutations have been essential for epidemiologic studies linking carcinogen exposure and cancer. We were concerned by the inclusion of dubious reports in the p53 databases that could lead to controversial analysis prejudicial to the scientific community.

EXPERIMENTAL DESIGN

We used the universal mutation database p53 database (21,717 mutations) combined with a new p53 mutant activity database (2,300 mutants) to perform functional analysis of 1,992 publications reporting p53 alterations. This analysis was done using a statistical approach similar to that of clinical meta-analyses.

RESULTS

This analysis reveals that some reports of infrequent mutations are associated with almost normal activities of p53 proteins. These particular mutations are frequently found in studies reporting multiple mutations in one tumor, silent mutations, or lacking mutation hotspots. These reports are often associated with particular methodologies, such as nested PCR, for which key controls are not satisfactory.

CONCLUSIONS

We show the importance of accurate functional analysis before inferring any genetic variation. The quality of the p53 databases is essential in order to prevent erroneous analysis and/or conclusions. The availability of functional data from our new p53 web site (http://p53.free.fr and http://www.umd.be:2072/) will allow functional prescreening to identify potential artifactual data.

摘要

目的

对p53突变模式的分析对于将致癌物暴露与癌症联系起来的流行病学研究至关重要。我们担心p53数据库中纳入了可疑报告,这可能导致有争议的分析,对科学界产生不利影响。

实验设计

我们使用通用突变数据库p53数据库(21,717个突变)与一个新的p53突变体活性数据库(2,300个突变体),对1,992篇报告p53改变的出版物进行功能分析。该分析采用了类似于临床荟萃分析的统计方法。

结果

该分析表明,一些关于罕见突变的报告与p53蛋白几乎正常的活性相关。这些特定突变经常出现在报告一个肿瘤中有多个突变、沉默突变或缺乏突变热点的研究中。这些报告通常与特定方法相关,如巢式PCR,其关键对照并不令人满意。

结论

我们展示了在推断任何基因变异之前进行准确功能分析的重要性。p53数据库的质量对于防止错误分析和/或结论至关重要。我们新的p53网站(http://p53.free.fr和http://www.umd.be:2072/)提供的功能数据将允许进行功能预筛选,以识别潜在的人为数据。

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