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用于胸腔积液中微小RNA相对定量分析的合适内参基因的鉴定

Identification of suitable reference genes for the relative quantification of microRNAs in pleural effusion.

作者信息

Han Hye-Suk, Jo Yeong Nang, Lee Jin Yong, Choi Song-Yi, Jeong Yusook, Yun Jieun, Lee Ok-Jun

机构信息

Department of Internal Medicine, College of Medicine, Chungbuk National University, Cheongju 361-763, Republic of Korea.

Bioevaluation Center, Korea Research Institute of Bioscience and Biotechnology, Cheongwon 363-883, Republic of Korea.

出版信息

Oncol Lett. 2014 Oct;8(4):1889-1895. doi: 10.3892/ol.2014.2404. Epub 2014 Aug 1.

Abstract

Circulating cell-free microRNAs (miRNAs) are potential biomarkers of cancer. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is widely used in miRNA expression studies. The aim of this study was to identify suitable reference genes for RT-qPCR analyses of miRNA expression levels in pleural effusion. The expression levels of candidate reference miRNAs were investigated in 10 benign pleural effusion (BPE) and 10 lung adenocarcinoma-associated malignant pleural effusion (LA-MPE) samples using miRNA microarrays. The expression levels of candidate reference miRNAs, together with those of U6 small nuclear RNA (snRNA), RNU6B, RNU44 and RNU48 small RNAs, in 46 BPE and 45 LA-MPE samples were validated by RT-qPCR, and were analyzed using the NormFinder and BestKeeper algorithms. The impact of different normalization approaches on the detection of differential expression levels of miR-198 in BPE and LA-MPE samples was also assessed. As determined by the miRNA microarray data, five candidate reference miRNAs were identified. Following RT-qPCR validation, U6 snRNA, miR-192, miR-20a, miR-221, miR-222 and miR-16 were evaluated using the NormFinder and BestKeeper software programs. U6 snRNA and miR-192 were identified as single reference genes and the combination of these genes was preferred for the relative quantification of miRNA expression levels in pleural effusion. Normalization of miR-98 expression levels to those of U6 snRNA, miR-192 or a combination of these genes enabled the detection of a significant difference between BPE and LA-MPE samples. Therefore, U6 snRNA and miR-192 are recommended as reference genes for the relative quantification of miRNA expression levels in pleural effusion.

摘要

循环游离微小RNA(miRNA)是癌症的潜在生物标志物。逆转录定量聚合酶链反应(RT-qPCR)广泛应用于miRNA表达研究。本研究的目的是鉴定用于RT-qPCR分析胸腔积液中miRNA表达水平的合适内参基因。使用miRNA芯片在10例良性胸腔积液(BPE)和10例肺腺癌相关恶性胸腔积液(LA-MPE)样本中研究候选内参miRNA的表达水平。通过RT-qPCR验证46例BPE和45例LA-MPE样本中候选内参miRNA以及U6小核RNA(snRNA)、RNU6B、RNU44和RNU48小RNA的表达水平,并使用NormFinder和BestKeeper算法进行分析。还评估了不同标准化方法对BPE和LA-MPE样本中miR-198差异表达水平检测的影响。根据miRNA芯片数据确定了5个候选内参miRNA。RT-qPCR验证后,使用NormFinder和BestKeeper软件程序评估U6 snRNA、miR-192、miR-20a、miR-221、miR-222和miR-16。U6 snRNA和miR-192被鉴定为单一内参基因,这些基因的组合更适合用于胸腔积液中miRNA表达水平的相对定量。将miR-98表达水平标准化为U6 snRNA、miR-192或这些基因的组合能够检测出BPE和LA-MPE样本之间的显著差异。因此,推荐U6 snRNA和miR-192作为胸腔积液中miRNA表达水平相对定量的内参基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc8/4156210/672886cde1be/OL-08-04-1889-g00.jpg

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