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Deleterious effects of formalin-fixation and delays to fixation on RNA and miRNA-Seq profiles

机译:福尔马林固定的有害作用和固定延迟对RNA和miRNA-Seq谱的影响

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摘要

The National Cancer Institute conducted the Biospecimen Pre-analytical Variables (BPV) study to determine the effects of formalin fixation and delay to fixation (DTF) on the analysis of nucleic acids. By performing whole transcriptome sequencing and small RNA profiling on matched snap-frozen and FFPE specimens exposed to different delays to fixation, this study aimed to determine acceptable delays to fixation and proper workflow for accurate and reliable Next-Generation Sequencing (NGS) analysis of FFPE specimens. In comparison to snap-freezing, formalin fixation changed the relative proportions of intronic/exonic/untranslated RNA captured by RNA-seq for most genes. The effects of DTF on NGS analysis were negligible. In 80% of specimens, a subset of RNAs was found to differ between snap-frozen and FFPE specimens in a consistent manner across tissue groups; this subset was unaffected in the remaining 20% of specimens. In contrast, miRNA expression was generally stable across various formalin fixation protocols, but displayed increased variability following a 12 h delay to fixation.
机译:美国国家癌症研究所进行了生物样本分析前变量(BPV)研究,以确定福尔马林固定和固定延迟(DTF)对核酸分析的影响。通过对暴露于不同固定延迟的匹配速冻和FFPE标本进行完整的转录组测序和小RNA谱分析,本研究旨在确定可接受的固定延迟和正确的工作流程,以进行FFPE的准确可靠的下一代测序(NGS)分析标本。与速冻相比,福尔马林固定改变了大多数基因被RNA-seq捕获的内含子/外显子/非翻译RNA的相对比例。 DTF对NGS分析的影响可以忽略不计。在80%的标本中,发现速冻和FFPE标本之间的RNA子集在各个组织组之间均一致。该子集在其余20%的样本中不受影响。相比之下,在各种福尔马林固定方案中,miRNA的表达通常是稳定的,但在固定12h后,其可变性却增加了。

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