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污染和样本混淆最能解释颊细胞和口腔鳞状细胞癌中线粒体DNA不稳定性的某些模式。

Contamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinoma.

作者信息

Bandelt Hans-Jürgen, Salas Antonio

机构信息

Department of Mathematics, University of Hamburg, 20146 Hamburg, Germany.

出版信息

BMC Cancer. 2009 Apr 16;9:113. doi: 10.1186/1471-2407-9-113.

Abstract

The study of somatic DNA instabilities constitutes a debatable topic because different causes can lead to seeming DNA alteration patterns between different cells or tissues from the same individual. Carcinogenesis or the action of a particular toxic could generate such patterns, and this is in fact the leitmotif of a number of studies on mitochondrial DNA (mtDNA) instability. Patterns of seeming instabilities could also arise from technical errors at any stage of the analysis (DNA extraction, amplification, mutation screening/sequencing, and documentation). Specifically, inadvertent DNA contamination or sample mixing would yield mosaic variation that could be erroneously interpreted as real mutation differences (instabilities) between tissues from the same individual. From the very beginning, mtDNA studies comparing cancerous to non-cancerous tissues have suffered from such mosaic results. We demonstrate here that the phylogenetic linkage of whole arrays of mtDNA mutations provides strong evidence of artificial recombination in previous studies on buccal cells and oral squamous cell carcinoma.

摘要

体细胞DNA不稳定性的研究是一个有争议的话题,因为不同的原因可能导致同一个体不同细胞或组织之间出现看似不同的DNA改变模式。致癌作用或特定毒素的作用可能产生这样的模式,而这实际上是许多关于线粒体DNA(mtDNA)不稳定性研究的主旨。看似不稳定的模式也可能源于分析的任何阶段(DNA提取、扩增、突变筛查/测序以及记录)的技术错误。具体而言,不经意的DNA污染或样本混合会产生嵌合变异,这可能被错误地解释为同一个体不同组织之间真正的突变差异(不稳定性)。从一开始,比较癌组织与非癌组织的mtDNA研究就受到了这种嵌合结果的困扰。我们在此证明,mtDNA突变整个阵列的系统发育联系为先前关于颊细胞和口腔鳞状细胞癌的研究中的人工重组提供了有力证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cdf/2678148/cf3513d3f999/1471-2407-9-113-1.jpg

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