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Evaluation of Storage Tubes for Combined Analysis of Circulating Nucleic Acids in Liquid Biopsies

机译:液体活检中循环核酸联合分析的储管评估

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摘要

In the last decade, circulating nucleic acids such as microRNAs (miRNAs) and cell-free DNA (cfDNA) have become increasingly important in serving as potential novel biomarkers for a variety of human diseases. If cell-free nucleic acids are to become routinely used in diagnostics, the difference in plasma miRNA and cfDNA levels between healthy and diseased subjects must exceed pre-analytical and analytical variability. Until now, few studies have addressed the time limitations of pre-processing or explored the potential use of long-term blood storage tubes, which might need to be implemented in real-life diagnostics. In this study, we analyzed the stability of four breast cancer-associated miRNAs and two cancer-associated genes under various storage conditions, to test their limitations for potential application in clinical diagnostics. In two consecutive experiments, we tested the limits of conventional EDTA tubes, as well as long-term storage blood collection tubes (BCTs) from four different manufacturers. We found that circulating miRNAs are relatively stable when stored in EDTA monovettes for up to 12 h before processing. When stored in BCTs, circulating miRNAs and cfDNA are stable for up to 7 days, depending on the manufacturer. Norgen tubes were superior for cfDNA yield, while Streck tubes performed the worst in our study with hemolysis induction. In conclusion, plasma prepared from whole blood is suitable for the quantification of both cf-miRNAs and cfDNA simultaneously.
机译:在过去的十年中,循环核酸(例如microRNA(miRNA)和无细胞DNA(cfDNA))在用作各种人类疾病的潜在新生物标记方面变得越来越重要。如果要在诊断中常规使用无细胞核酸,那么健康受试者和患病受试者之间血浆miRNA和cfDNA的差异必须超过分析和分析的可变性。到目前为止,很少有研究解决预处理的时间限制或探索长期储血管的潜在用途,而这可能需要在现实生活中进行诊断。在这项研究中,我们分析了四个乳腺癌相关的miRNA和两个癌症相关的基因在各种存储条件下的稳定性,以测试它们在临床诊断中潜在应用的局限性。在两个连续的实验中,我们测试了传统EDTA管的极限以及来自四个不同制造商的长期存储采血管(BCT)。我们发现,在处理之前,循环的miRNA在EDTA monovettes中存储长达12 h时相对稳定。当储存在BCT中时,循环的miRNA和cfDNA最多可稳定7天,具体取决于制造商。诺根管的cfDNA产量更高,而Streck管在我们的溶血诱导研究中表现最差。总之,从全血中制备的血浆适合同时定量cf-miRNA和cfDNA。

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