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在葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠模型的存档福尔马林固定石蜡包埋(FFPE)结肠样本中进行表达研究(qPCR)时mRNA和miRNA内参基因的选择与评估

Selection and Evaluation of mRNA and miRNA Reference Genes for Expression Studies (qPCR) in Archived Formalin-Fixed and Paraffin-Embedded (FFPE) Colon Samples of DSS-Induced Colitis Mouse Model.

作者信息

Unkovič Ana, Boštjančič Emanuela, Belič Aleš, Perše Martina

机构信息

Medical Experimental Centre, Institute of Pathology, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.

Institute of Pathology, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.

出版信息

Biology (Basel). 2023 Jan 26;12(2):190. doi: 10.3390/biology12020190.

Abstract

The choice of appropriate reference genes is essential for correctly interpreting qPCR data and results. However, the majority of animal studies use a single reference gene without any prior evaluation. Therefore, many qPCR results from rodent studies can be misleading, affecting not only reproducibility but also translatability. In this study, the expression stability of reference genes for mRNA and miRNA in archived FFPE samples of 117 C57BL/6JOlaHsd mice (males and females) from 9 colitis experiments (dextran sulfate sodium; DSS) were evaluated and their expression analysis was performed. In addition, we investigated whether normalization reduced/neutralized the influence of inter/intra-experimental factors which we systematically included in the study. Two statistical algorithms (NormFinder and Bestkeeper) were used to determine the stability of reference genes. Multivariate analysis was made to evaluate the influence of normalization with different reference genes on target gene expression in regard to inter/intra-experimental factors. Results show that archived FFPE samples are a reliable source of RNA and imply that the FFPE procedure does not change the ranking of stability of reference genes obtained in fresh tissues. Multivariate analysis showed that the histological picture is an important factor affecting the expression levels of target genes.

摘要

选择合适的内参基因对于正确解读qPCR数据和结果至关重要。然而,大多数动物研究仅使用单个内参基因,且未进行任何预先评估。因此,许多啮齿动物研究的qPCR结果可能会产生误导,不仅影响可重复性,还影响可转化性。在本研究中,我们评估了来自9项结肠炎实验(葡聚糖硫酸钠;DSS)的117只C57BL/6JOlaHsd小鼠(雄性和雌性)存档FFPE样本中mRNA和miRNA内参基因的表达稳定性,并进行了表达分析。此外,我们研究了标准化是否减少/中和了我们在研究中系统纳入的实验间/实验内因素的影响。使用两种统计算法(NormFinder和Bestkeeper)来确定内参基因的稳定性。进行多变量分析以评估使用不同内参基因进行标准化对实验间/实验内因素下目标基因表达的影响。结果表明,存档的FFPE样本是可靠的RNA来源,这意味着FFPE处理过程不会改变在新鲜组织中获得的内参基因稳定性排名。多变量分析表明,组织学图像是影响目标基因表达水平的重要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/9952917/8a2c7fa7c993/biology-12-00190-g001.jpg

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