Clinical Biochemistry section, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Colorectal & Peritoneal Oncology Centre, The Christie NHS Foundation Trust, Manchester, Manchester, M20 4BX, United Kingdom.
Sci Rep. 2017 Aug 21;7(1):8413. doi: 10.1038/s41598-017-08784-3.
MicroRNAs (miRNAs) hold great promise in cancer research. The use of appropriate reference miRNAs for normalization of qPCR data is crucial for accurate expression analysis. We present here analysis and verification of current data, proposing a workflow strategy for identification of reference miRNAs in colorectal cancer (CRC). We performed a systematic review of studies aimed to identify stable reference miRNAs in CRC through high-throughput screening. Among the candidate miRNAs selected from the literature we excluded those predicted to target oncogenes or tumor suppressor gene. We then assessed the expression levels of the remaining candidates in exosomes, plasma and tissue samples from CRC patients and healthy controls. The expression stability was evaluated by box-plot, ∆Cq analysis, NormFinder and BestKeeper statistical algorithms. The effects of normalisers on the relative quantification of the oncogenic miR-1290 was also assessed. Our results consistently showed that different combinations of miR-520d, miR-1228 and miR-345 provided the most stably expressed reference miRNAs in the three biological matrices. We identified suitable reference miRNAs for future miRNA expression studies in exosomes plasma and tissues CRC samples. We also provided a novel conceptual framework that overcome the need of performing ex novo identification of suitable reference genes in single experimental systems.
微小 RNA(miRNA)在癌症研究中具有巨大的潜力。使用适当的参考 miRNA 对 qPCR 数据进行标准化对于准确的表达分析至关重要。我们在此呈现了对现有数据的分析和验证,提出了一种用于鉴定结直肠癌(CRC)中参考 miRNA 的工作流程策略。我们通过高通量筛选对旨在鉴定 CRC 中稳定参考 miRNA 的研究进行了系统评价。从文献中选择的候选 miRNA 中,我们排除了那些预测靶向癌基因或肿瘤抑制基因的 miRNA。然后,我们评估了来自 CRC 患者和健康对照的外泌体、血浆和组织样本中剩余候选物的表达水平。通过箱线图、∆Cq 分析、NormFinder 和 BestKeeper 统计算法评估表达稳定性。还评估了归一化因子对致癌 miR-1290 相对定量的影响。我们的结果一致表明,miR-520d、miR-1228 和 miR-345 的不同组合在三种生物基质中提供了最稳定表达的参考 miRNA。我们鉴定了适用于未来在 exosomes plasma 和组织 CRC 样本中进行 miRNA 表达研究的参考 miRNA。我们还提供了一种新的概念框架,克服了在单个实验系统中进行新的合适参考基因识别的需要。