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Selection and validation of endogenous controls for microRNA expression studies in endometrioid endometrial cancer tissues

机译:子宫内膜样子宫内膜癌组织中microRNA表达研究的内源性对照的选择和验证

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Objectives microRNAs comprise a family of small, non-coding RNAs, which regulate gene expression at the posttranscriptional level. Multiple studies implicated important roles of microRNAs in various malignancies including endometrioid endometrial carcinoma (EEC). qPCR is widely used in the studies investigating microRNA expression. Relative quantification of microRNA expression requires proper normalization methods and endogenous controls are widely used for this purpose. The aim of this study was experimental identification of stable endogenous controls for normalization of microRNA qPCR expression studies in EEC. Methods Expression of twelve candidate endogenous controls (miR-16, miR-26b, miR-92a, RNU44, RNU48, U75, U54, U6, U49, RNU6B, RNU38B, U18A) was investigated in tissue samples obtained from 45 patients (30 EEC, 15 normal endometrium) using qPCR. Stability of candidate endogenous controls was evaluated using NormFinder, geNorm, BestKeeper and equivalency test. The results were then validated using larger group of samples. Results RNU48, U75 and RNU44 were identified as stably and equivalently expressed between malignant and normal tissues. Both NormFinder and geNorm indicated that those three snRNAs were optimal for qPCR data normalization in EEC tissues. Conclusions In conclusion, we suggest that average expression of those snoRNAs could be used as a reliable endogenous control in microRNA qPCR studies in endometrioid endometrial cancer. In addition to identifying suitable endogenous controls in EEC, our study presents an appropriate strategy for validation of candidate reference genes for any microRNA qPCR study.
机译:目标microRNA包括一个小的非编码RNA家族,它们在转录后水平上调节基因表达。多项研究表明microRNA在包括子宫内膜样子宫内膜癌(EEC)在内的各种恶性肿瘤中的重要作用。 qPCR被广泛用于研究microRNA表达的研究中。 microRNA表达的相对定量需要适当的标准化方法,并且内源性对照广泛用于此目的。这项研究的目的是实验鉴定稳定的内源性对照,以使EEC中的microRNA qPCR表达研究正常化。方法在45例患者(30例EEC)的组织样本中研究了十二种候选内源性对照(miR-16,miR-26b,miR-92a,RNU44,RNU48,U75,U54,U6,U49,RNU6B,RNU38B,U18A)的表达,15个正常子宫内膜)。使用NormFinder,geNorm,BestKeeper和等效性测试评估候选内源性对照的稳定性。然后使用较大的样本组验证结果。结果RNU48,U75和RNU44在恶性组织和正常组织中被稳定表达。 NormFinder和geNorm均表明,这三种snRNA最适合EEC组织中qPCR数据的标准化。结论总之,我们建议这些snoRNA的平均表达可以用作子宫内膜样子宫内膜癌的microRNA qPCR研究中的可靠内源性对照。除了在EEC中确定合适的内源性对照外,我们的研究还提出了用于验证任何microRNA qPCR研究的候选参考基因的合适策略。

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