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评估 miRNA 检测方法的临床应用分析特性。

Evaluation of miRNA detection methods for the analytical characteristic necessary for clinical utilization.

机构信息

Central European Institute of Technology, Masaryk University, Brno, Czech Republic.

BioVendor - Laboratorní medicína a.s., Brno, Czech Republic.

出版信息

Biotechniques. 2019 Jun;66(6):277-284. doi: 10.2144/btn-2019-0021. Epub 2019 May 24.

Abstract

miRNAs are promising biomarkers but methods for their measurement are not clear. We therefore examined three miRNA detection technologies and considered the analytical characteristics essential for clinical utilization. TaqMan assays, SplintR-qPCR and miREIA were compared for their absolute quantification bias, conformity and robustness. Absolute concentrations of miR-142-5p, miR-23a-3p and miR-93-5p were measured with all three methods using 30 samples. Robustness was evaluated by measurement of miR-21-5p in five uniform experiments. Correlations were miRNA-specific, but we observed a different absolute concentration range in RT-qPCR (fmol/μl) and methods evading the RT process (amol/μl). Consistently, RT-less methods reported better robustness (CV 8-19%) than RT-qPCR (CV 39-50%). The calibration curve in TaqMan Advanced assay was influenced by dilution media. Methods avoiding RT seem to be a promising future alternative for miRNA measurement.

摘要

miRNAs 是很有前途的生物标志物,但它们的测量方法尚不清楚。因此,我们研究了三种 miRNA 检测技术,并考虑了对临床应用至关重要的分析特性。我们比较了 TaqMan 检测、SplintR-qPCR 和 miREIA 在绝对定量偏差、一致性和稳健性方面的表现。使用这三种方法对 30 个样本中的 miR-142-5p、miR-23a-3p 和 miR-93-5p 进行绝对浓度检测。使用五个均匀实验测量 miR-21-5p 来评估稳健性。相关性是 miRNA 特异性的,但我们在 RT-qPCR(fmol/μl)和避免 RT 过程的方法(amol/μl)中观察到不同的绝对浓度范围。一致的是,无 RT 方法(CV 8-19%)比 RT-qPCR(CV 39-50%)报告了更好的稳健性。TaqMan 高级检测中的校准曲线受到稀释介质的影响。避免 RT 的方法似乎是 miRNA 测量的有前途的未来替代方法。

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