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Analysis of biological and technical variability in gene expression assays from formalin-fixed paraffin-embedded classical Hodgkin lymphomas

机译:福尔马林固定石蜡包埋的经典霍奇金淋巴瘤基因表达测定的生物学和技术变异性分析

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Formalin-fixed paraffin-embedded (FFPE) tissues are invaluable sources of biological material for research and diagnostic purposes. In this study, we aimed to identify biological and technical variability in RT-qPCR TaqMan (R)) assays performed with FFPE-RNA from lymph nodes of classical Hodgkin lymphoma samples. An ANOVA-nested 6-level design was employed to evaluate BCL2, CASP3, IRF4, LYZ and STAT1 gene expression. The most variable genes were CASP3 (low expression) and LYZ (high expression). Total variability decreased after normalization for all genes, except by LYZ. Genes with moderate and low expression were identified and suffered more the effects of the technical manipulation than high-expression genes. Pre-amplification was shown to introduce significant technical variability, which was partially alleviated by lowering to a half the amount of input RNA. Ct and Cyo quantification methods, based on cycle-threshold and the kinetic of amplification curves, respectively, were compared. Cyo method resulted in higher quantification values, leading to the decrease of total variability in CASP3 and LYZ genes. The mean individual noise was 0.45 (0.31 to 0.61 SD), indicating a variation of gene expression over similar to 1.5 folds from one case to another. We showed that total variability in RT-qPCR from FFPE-RNA is not higher than that reported for fresh complex tissues, and identified gene-, and expression level-sources of biological and technical variability, which can allow better strategies for designing RT-qPCR assays from highly degraded and inhibited samples. (C) 2014 Elsevier Inc. All rights reserved.
机译:福尔马林固定石蜡包埋(FFPE)组织是用于研究和诊断目的的宝贵生物材料来源。在这项研究中,我们旨在确定从经典霍奇金淋巴瘤样本的淋巴结中使用FFPE-RNA进行的RT-qPCR TaqMan(R)分析中的生物学和技术差异。采用ANOVA嵌套的6级设计评估BCL2,CASP3,IRF4,LYZ和STAT1基因的表达。可变性最高的基因是CASP3(低表达)和LYZ(高表达)。除LYZ外,所有基因标准化后的总变异性降低。鉴定出具有中等和低表达的基因,与高表达基因相比,它们遭受的技术操纵影响更大。预先扩增显示出显着的技术变异性,通过将输入RNA降低一半来部分缓解。比较了分别基于循环阈值和扩增曲线动力学的Ct和Cyo定量方法。 Cyo方法导致较高的定量值,从而导致CASP3和LYZ基因的总变异性降低。平均个体噪声为0.45(0.31到0.61 SD),表明从一种情况到另一种情况,基因表达的变化约为1.5倍。我们显示,FFPE-RNA的RT-qPCR的总变异性不高于新鲜复杂组织的报道,并且已鉴定出生物学和技术变异性的基因和表达水平来源,这可以为设计RT-qPCR提供更好的策略从高度降解和抑制的样品中进行检测。 (C)2014 Elsevier Inc.保留所有权利。

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