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用于福尔马林固定石蜡包埋(FFPE)组织芯的商用RNA和DNA提取试剂盒的可靠性和性能

Reliability and performance of commercial RNA and DNA extraction kits for FFPE tissue cores.

作者信息

Patel Palak G, Selvarajah Shamini, Guérard Karl-Philippe, Bartlett John M S, Lapointe Jacques, Berman David M, Okello John B A, Park Paul C

机构信息

Department of Pathology & Molecular Medicine, Queen's University, Kingston, Ontario, Canada.

Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Queen's University, Kingston, Ontario, Canada.

出版信息

PLoS One. 2017 Jun 22;12(6):e0179732. doi: 10.1371/journal.pone.0179732. eCollection 2017.

Abstract

Cancer biomarker studies often require nucleic acid extraction from limited amounts of formalin-fixed, paraffin-embedded (FFPE) tissues, such as histologic sections or needle cores. A major challenge is low quantity and quality of extracted nucleic acids, which can limit our ability to perform genetic analyses, and have a significant influence on overall study design. This study was aimed at identifying the most reliable and reproducible method of obtaining sufficient high-quality nucleic acids from FFPE tissues. We compared the yield and quality of nucleic acids from 0.6-mm FFPE prostate tissue cores across 16 DNA and RNA extraction protocols, using 14 commercially available kits. Nucleic acid yield was determined by fluorometry, and quality was determined by spectrophotometry. All protocols yielded nucleic acids in quantities that are compatible with downstream molecular applications. However, the protocols varied widely in the quality of the extracted RNA and DNA. Four RNA and five DNA extraction protocols, including protocols from two kits for dual-extraction of RNA and DNA from the same tissue source, were prioritized for further quality assessment based on the yield and purity of their products. Specifically, their compatibility with downstream reactions was assessed using both NanoString nCounter gene expression assays and reverse-transcriptase real-time PCR for RNA, and methylation-specific PCR assays for DNA. The kit deemed most suitable for FFPE tissue was the AllPrep kit by Qiagen because of its yield, quality, and ability to purify both RNA and DNA from the same sample, which would be advantageous in biomarker studies.

摘要

癌症生物标志物研究通常需要从有限量的福尔马林固定石蜡包埋(FFPE)组织中提取核酸,如组织学切片或针芯。一个主要挑战是提取的核酸数量少且质量低,这可能会限制我们进行基因分析的能力,并对整体研究设计产生重大影响。本研究旨在确定从FFPE组织中获得足够高质量核酸的最可靠且可重复的方法。我们使用14种市售试剂盒,比较了16种DNA和RNA提取方案从0.6毫米FFPE前列腺组织芯中提取核酸的产量和质量。通过荧光法测定核酸产量,通过分光光度法测定质量。所有方案产生的核酸数量均与下游分子应用兼容。然而,各方案提取的RNA和DNA质量差异很大。基于产品的产量和纯度,四种RNA和五种DNA提取方案(包括来自两种试剂盒的从同一组织来源同时提取RNA和DNA的方案)被优先进行进一步的质量评估。具体而言,使用NanoString nCounter基因表达测定法和RNA的逆转录实时PCR以及DNA的甲基化特异性PCR测定法评估它们与下游反应的兼容性。由于其产量、质量以及从同一样本中纯化RNA和DNA的能力,Qiagen公司的AllPrep试剂盒被认为最适合FFPE组织,这在生物标志物研究中具有优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ea/5480995/bc44bf6c99fb/pone.0179732.g001.jpg

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