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Quantitative analysis of noncoding RNA from paired fresh and formalin-fixed paraffin-embedded brain tissues

机译:配对新鲜和福尔马林固定石蜡包埋脑组织非沉积RNA的定量分析

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Formalin-fixed paraffin-embedded (FFPE) tissues are commonly used both clinically and in forensic pathology. Recently, noncoding RNA (ncRNA) has attracted interest among molecular medical researchers. However, it remains unclear whether newly identified ncRNAs, such as long noncoding RNA (lncRNA) and circular RNA (circRNA), remain stable for downstream molecular analysis in FFPE tissues. Here, we assessed the feasibility of using autoptic FFPE brain tissues from eight individuals to perform quantitative molecular analyses. Selected RNA targets (9 mRNAs and 15 ncRNAs) with different amplicon lengths were studied by RT-qPCR in paired fresh and FFPE specimens. For RNA quality assessment, RNA purity and yield were comparable between the two sample cohorts; however, the RNA integrity number decreased significantly during FFPE sampling. Amplification efficiency also displayed certain variability related with amplicon length and RNA species. We found molecular evidence that short amplicons of mRNA, lncRNA, and circRNA were amplified more efficiently than long amplicons. With the assistance of RefFinder, 5S, SNORD48, miR-103a, and miR-125b were selected as reference genes given their high stability. After normalization, we found that short amplicon markers (e.g., ACTB mRNA and MALAT1 lncRNA) exhibited high consistency of quantification in paired fresh/FFPE samples. In particular, circRNAs (XPO1, HIPK3, and TMEM56) presented relatively consistent and stable expression profiles in FFPE tissues compared with their corresponding linear transcripts. Additionally, we evaluated the influence of prolonged storage time on the amplification of gene transcripts and found that short amplicons still work effectively in archived FFPE biospecimens. In conclusion, our findings demonstrate the possibility of performing accurate quantitative analysis of ncRNAs using short amplicons and standardized RT-qPCR assays in autopsy-derived FFPE samples.
机译:福尔马林固定的石蜡包埋(FFPE)组织通常在临床上和法医病理学中使用。最近,Noncoding RNA(NCRNA)引起了分子医学研究人员的兴趣。然而,它仍然不清楚是否新鉴定的NCRNA,例如长的非分量RNA(LNCRNA)和圆形RNA(CircrNA),在FFPE组织中的下游分子分析保持稳定。在这里,我们评估了使用来自八个人的Autoptic FFPE脑组织进行定量分子分析的可行性。通过RT-QPCR在配对的新鲜和FFPE样本中研究具有不同扩增子长度的所选RNA靶标(9mRNA和15 NCRNA)。对于RNA质量评估,两个样品队列之间的RNA纯度和产率可相当;然而,在FFPE取样过程中,RNA完整性值显着下降。扩增效率也显示出与扩增子长度和RNA物种相关的某些可变性。我们发现分子证据表明,比长扩增子更有效地扩增mRNA,LNCRNA和CircrNA的短扩增子。在Reffinder,5s,Snord48,miR-103a和miR-125b的帮助下,作为其高稳定性选择作为参考基因。在归一化之后,我们发现短的扩增子标记(例如,ActB mRNA和Malat1 LncrNa)在配对的新鲜/ FFPE样品中表现出高一致性的定量。特别地,与相应的线性转录物相比,CiRCRNA(XPO1,HiPK3和TMEM56)在FFPE组织中呈现相对一致且稳定的表达谱。此外,我们评估了长期储存时间对基因转录物扩增的影响,发现短扩增子仍然有效地在存档的FFPE生物组织中工作。总之,我们的研究结果证明了使用短扩增子和尸检衍生的FFPE样品中的短大扩增子和标准化的RT-QPCR测定对NCRNA进行准确定量分析的可能性。

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