Department of Pathology, Chicago Medical School, North Chicago, Illinois 60064, USA.
J Mol Diagn. 2012 Jan;14(1):71-80. doi: 10.1016/j.jmoldx.2011.09.002. Epub 2011 Nov 30.
Circulating microRNAs (miRNAs) have emerged as candidate biomarkers of various diseases and conditions including malignancy and pregnancy. This approach requires sensitive and accurate quantitation of miRNA concentrations in body fluids. Herein we report that enzyme-based miRNA quantitation, which is currently the mainstream approach for identifying differences in miRNA abundance among samples, is skewed by endogenous serum factors that co-purify with miRNAs and anticoagulant agents used during collection. Of importance, different miRNAs were affected to varying extent among patient samples. By developing measures to overcome these interfering activities, we increased the accuracy, and improved the sensitivity of miRNA detection up to 30-fold. Overall, the present study outlines key factors that prevent accurate miRNA quantitation in body fluids and provides approaches that enable faithful quantitation of miRNA abundance in body fluids.
循环 microRNAs(miRNAs)已成为各种疾病和病症(包括恶性肿瘤和妊娠)的候选生物标志物。这种方法需要在体液中对 miRNA 浓度进行敏感和准确的定量。本文报道了基于酶的 miRNA 定量方法,这是目前用于识别样品中 miRNA 丰度差异的主流方法,但受到与 miRNA 共纯化的内源性血清因子和采集过程中使用的抗凝剂的影响。重要的是,不同的 miRNA 在患者样本中受到的影响程度不同。通过开发克服这些干扰活性的措施,我们将 miRNA 检测的准确性提高了 30 倍,灵敏度也提高了。总的来说,本研究概述了阻碍体液中准确 miRNA 定量的关键因素,并提供了能够真实定量体液中 miRNA 丰度的方法。