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人类癌细胞系中p53突变状态的分析:细胞系交叉污染的一个范例

Analysis of p53 mutation status in human cancer cell lines: a paradigm for cell line cross-contamination.

作者信息

Berglind Hanna, Pawitan Yudi, Kato Shunsuke, Ishioka Chikashi, Soussi Thierry

机构信息

Karolinska Institute, Department of Oncology-Pathology, Cancer Center Karolinska (CCK), Stockholm, Sweden.

出版信息

Cancer Biol Ther. 2008 May;7(5):699-708. doi: 10.4161/cbt.7.5.5712. Epub 2008 May 11.

Abstract

Cancer cell lines are essential tools used in many areas of biomedical research. Using the last release of the UMD_p53 database (2007) (http://p53.free.fr), we analysed the p53 status of 1,211 cell lines published between 1989 and 2007. p53 mutations in cell lines from various types of cancers display a striking similarity in the distribution of mutations and in the pattern of mutational events compared to tumors, indicating that they are representative of the cells from which they were derived. Analysis of the residual transcriptional activity of p53 mutants identified in cell lines that displayed two different p53 mutations show that there is a high frequency of weak mutations that are paired with more potent mutations suggesting a driver/passenger configuration. Strikingly, we found discrepancies in the p53 status for 23% (88/384) of cell lines, for which the p53 status was established independently in two laboratories. Using the NCI-60 cell line panel as a model widely used in the literature, the p53 status could not be ascertained for 13 cell lines due to a lack of homogeneous data in the literature. Our study clearly confirms that misidentified cell lines are still a silent and neglected danger and that extreme care should be taken as a wrong p53 status could lead to disastrous experimental interpretations. The p53 web site has been updated with new sections describing the p53 status in the majority of cell lines and a special section devoted to cell lines with controversial p53 status.

摘要

癌细胞系是生物医学研究诸多领域中不可或缺的工具。利用UMD_p53数据库的最新版本(2007年)(http://p53.free.fr),我们分析了1989年至2007年间发表的1211个细胞系的p53状态。与肿瘤相比,来自各种癌症类型的细胞系中的p53突变在突变分布和突变事件模式上显示出惊人的相似性,表明它们代表了其来源的细胞。对在显示两种不同p53突变的细胞系中鉴定出的p53突变体的残余转录活性进行分析表明,存在高频率的弱突变与更强效的突变配对,提示存在驱动/乘客配置。引人注目的是,我们发现23%(88/384)的细胞系在p53状态上存在差异,这些细胞系的p53状态是在两个实验室分别独立确定的。以文献中广泛使用的NCI - 60细胞系面板为模型,由于文献中缺乏统一数据,有13个细胞系的p53状态无法确定。我们的研究明确证实,错误鉴定的细胞系仍然是一个无声且被忽视的危险,并且应格外小心,因为错误的p53状态可能导致灾难性的实验解读。p53网站已更新,新增了描述大多数细胞系中p53状态的章节以及专门针对p53状态存在争议的细胞系的章节。

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