Suppr超能文献

数字PCR用于鉴别嵌合缺失以及确定标本中肿瘤细胞的比例。

Digital PCR for discriminating mosaic deletions and for determining proportion of tumor cells in specimen.

作者信息

Kluwe Lan

机构信息

Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Department of Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Eur J Hum Genet. 2016 Nov;24(11):1644-1648. doi: 10.1038/ejhg.2016.56. Epub 2016 Jun 8.

Abstract

Mosaicism, presence of a genetic feature in only a subpopulation of cells, is frequent in de novo genetic diseases. Among large deletions covering the NF1 tumor suppressor gene, the frequency of mosaicism can be as high as 40% in de novo patients. In this study, we demonstrate the high potential of digital PCR in detecting large NF1 deletions and in discriminating mosaic cases. By simultaneously assessing the NF1 gene and a reference gene RPP30, deletions could be unambiguously distinguished from non-deletion samples. Performing the same assay for mixed samples from a DNA with a deletion and a non-deletion DNA, a highly significant linear relation was obtained between the set-up ratio of the two samples and the measured ratio of NF1/RPP30 (P<0.0001), suggesting the high potential of digital PCR in discriminating mosaic deletions. Furthermore, digital PCR detects NF1 allele loss in a tumor specimen that was not detected by loss of heterozygosity analysis using polymorphic markers due to high content of non-tumor cells. Based on the measured ratio of NF1/RPP30, the proportion of the tumor cells in this specimen could be calculated as 25%. Our results demonstrate that dual-probe digital PCR is a simple and effective method for detecting deletions and for discriminating mosaic deletions. Furthermore, this method is sensitive for assigning somatic allele loss in tumor specimen and enables determining proportion of tumor cells.

摘要

嵌合体现象,即仅在部分细胞亚群中存在的一种遗传特征,在新发遗传病中很常见。在覆盖NF1肿瘤抑制基因的大片段缺失中,新发患者中嵌合体的发生率可高达40%。在本研究中,我们证明了数字PCR在检测NF1大片段缺失和区分嵌合病例方面具有很高的潜力。通过同时评估NF1基因和一个参考基因RPP30,可以明确区分缺失样本和非缺失样本。对来自一个有缺失的DNA和一个无缺失的DNA的混合样本进行相同的检测,两个样本的设置比例与测量的NF1/RPP30比例之间获得了高度显著的线性关系(P<0.0001),这表明数字PCR在区分嵌合缺失方面具有很高的潜力。此外,数字PCR检测到了一个肿瘤标本中的NF1等位基因缺失,而由于非肿瘤细胞含量高,使用多态性标记进行杂合性缺失分析未检测到该缺失。根据测量的NF1/RPP30比例,该标本中肿瘤细胞的比例可计算为25%。我们的结果表明,双探针数字PCR是一种检测缺失和区分嵌合缺失的简单有效的方法。此外,该方法在确定肿瘤标本中的体细胞等位基因缺失方面很敏感,并能够确定肿瘤细胞的比例。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验