Asaga Sota, Hoon Dave S B
Department of Molecular Oncology, John Wayne Cancer Institute at Saint John's Health Center, Santa Monica, CA, USA.
Methods Mol Biol. 2013;1024:147-55. doi: 10.1007/978-1-62703-453-1_11.
MicroRNAs (miRs) are small noncoding RNAs which can be detected in body fluids as well as cells and tissues. miRs play important roles in various activities of cancer cells. The miRs in bloods called circulating miRs (cmiRs) are potential biomarkers for detecting and monitoring cancer progression. There are reports on the cmiR research which utilizes various primers, reagents, and instruments. Here, we introduce our protocols for RNA extraction and RT-qPCR for cmiRs as well as our novel RT-qPCR directly in serum assay (RT-qPCR-DS) where RT is directly performed in serum without the need for RNA extraction. Results from the two protocols are analyzed and compared. RT-qPCR-DS is logistically simpler and more sensitive in assessing cmiR in breast cancer patients than isolating RNA before RT-qPCR. This approach may be very useful as a diagnostic tool.
微小RNA(miRs)是一类小的非编码RNA,可在体液以及细胞和组织中检测到。miRs在癌细胞的各种活动中发挥重要作用。血液中的miRs称为循环miRs(cmiRs),是检测和监测癌症进展的潜在生物标志物。有关于利用各种引物、试剂和仪器进行cmiR研究的报道。在此,我们介绍了用于cmiRs的RNA提取和RT-qPCR的方案,以及我们直接在血清中进行的新型RT-qPCR检测(RT-qPCR-DS),即在血清中直接进行逆转录,无需RNA提取。对这两种方案的结果进行了分析和比较。与在RT-qPCR之前分离RNA相比,RT-qPCR-DS在评估乳腺癌患者的cmiR方面在逻辑上更简单且更灵敏。这种方法作为一种诊断工具可能非常有用。