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多中心 FFPE 组织核酸提取验证研究。

Multicentre validation study of nucleic acids extraction from FFPE tissues.

机构信息

ACADEM Department-University of Trieste and ICGEB, University of Trieste, Cattinara Hospital, 34149 Trieste, Italy.

出版信息

Virchows Arch. 2010 Sep;457(3):309-17. doi: 10.1007/s00428-010-0917-5. Epub 2010 Jul 28.

Abstract

In most pathology laboratories worldwide, formalin-fixed paraffin embedded (FFPE) samples are the only tissue specimens available for routine diagnostics. Although commercial kits for diagnostic molecular pathology testing are becoming available, most of the current diagnostic tests are laboratory-based assays. Thus, there is a need for standardized procedures in molecular pathology, starting from the extraction of nucleic acids. To evaluate the current methods for extracting nucleic acids from FFPE tissues, 13 European laboratories, participating to the European FP6 program IMPACTS (www.impactsnetwork.eu), isolated nucleic acids from four diagnostic FFPE tissues using their routine methods, followed by quality assessment. The DNA-extraction protocols ranged from homemade protocols to commercial kits. Except for one homemade protocol, the majority gave comparable results in terms of the quality of the extracted DNA measured by the ability to amplify differently sized control gene fragments by PCR. For array-applications or tests that require an accurately determined DNA-input, we recommend using silica based adsorption columns for DNA recovery. For RNA extractions, the best results were obtained using chromatography column based commercial kits, which resulted in the highest quantity and best assayable RNA. Quality testing using RT-PCR gave successful amplification of 200 bp-250 bp PCR products from most tested tissues. Modifications of the proteinase-K digestion time led to better results, even when commercial kits were applied. The results of the study emphasize the need for quality control of the nucleic acid extracts with standardised methods to prevent false negative results and to allow data comparison among different diagnostic laboratories.

摘要

在世界上大多数病理实验室中,福尔马林固定石蜡包埋(FFPE)样本是唯一可用于常规诊断的组织标本。尽管商业试剂盒可用于诊断分子病理学检测,但大多数当前的诊断测试都是基于实验室的检测方法。因此,需要从提取核酸开始,制定标准化的分子病理学程序。

为了评估从 FFPE 组织中提取核酸的当前方法,参与欧盟第六框架计划 IMPACTS(www.impactsnetwork.eu)的 13 个欧洲实验室使用其常规方法从四种诊断性 FFPE 组织中分离核酸,然后进行质量评估。DNA 提取方案从自制方案到商业试剂盒不等。除了一种自制方案外,大多数方案在通过 PCR 扩增不同大小的对照基因片段的能力方面,都可以提供可比的提取 DNA 质量结果。对于阵列应用或需要准确确定 DNA 输入的测试,我们建议使用基于硅的吸附柱回收 DNA。对于 RNA 提取,基于色谱柱的商业试剂盒获得了最佳结果,得到了最高数量和最佳可检测 RNA。使用 RT-PCR 进行质量测试,从大多数测试组织中成功扩增了 200 bp-250 bp 的 PCR 产物。甚至在应用商业试剂盒时,通过改变蛋白酶 K 消化时间也可以获得更好的结果。

研究结果强调了需要使用标准化方法对核酸提取物进行质量控制,以防止假阴性结果,并允许不同诊断实验室之间的数据比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7616/2933807/7b3946a587e1/428_2010_917_Fig1_HTML.jpg

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