Uray Iván P, László Loretta
Faculty of Medicine, Department of Clinical Oncology, University of Debrecen, Debrecen, Hungary.
Methods Mol Biol. 2019;2019:225-236. doi: 10.1007/978-1-4939-9585-1_16.
Retinoids and rexinoids directly and selectively activate their nuclear receptors, resulting in changes in the transcript levels of their target genes. Consequently, quantitating mRNA levels transcribed from cognate target genes is the most accurate measure of retinoid action. These changes can serve as relevant endpoints in biomarker trials, as well as in vivo preclinical studies. In gene expression analyses of archival material such as formalin-fixed paraffin-embedded (FFPE) tissues, assessing the quality of the extracted RNA is essential for the validation of the studies. With next generation sequencing (NGS) becoming the method of choice for gene expression profiling, RNA quality has become a critical aspect of study feasibility. In this chapter, we describe a method to extract RNA and to assess the intactness of RNA samples extracted from paraffin-embedded tissues.
类视黄醇和类视黄酸X受体激动剂直接且选择性地激活其核受体,导致其靶基因转录水平发生变化。因此,定量源自同源靶基因的mRNA水平是衡量类视黄醇作用的最准确方法。这些变化可作为生物标志物试验以及体内临床前研究的相关终点。在对福尔马林固定石蜡包埋(FFPE)组织等存档材料进行基因表达分析时,评估提取RNA的质量对于研究的验证至关重要。随着下一代测序(NGS)成为基因表达谱分析的首选方法,RNA质量已成为研究可行性的关键因素。在本章中,我们描述了一种从石蜡包埋组织中提取RNA并评估所提取RNA样品完整性的方法。