Direct S-Poly(T) Plus assay in quantification of microRNAs without RNA extraction and its implications in colorectal cancer biomarker studies.

J Transl Med

Shenzhen Key Laboratory of Microbial Genetic Engineering, Vascular Disease Research Center, Guangdong Provincial Key Laboratory of Regional Immunity and Diseases, Carson International Cancer Center, College of Life Sciences and Oceanography, Shenzhen University, Nanhai Ave 3688, Shenzhen, 518060, Guangdong, China.

Published: September 2019

Background: Advances in microRNAs (miRNAs) biomarkers have generated disease markers with potential clinical values. However, none of these published results have been applied in clinic until today. The main reason could be the lack of simple but robust miRNA measurements.

Methods: We built up a simple but ultrasensitive RT-qPCR protocol, Direct S-Poly(T) Plus assay, for detecting miRNAs without RNA purification. In this study, the method was optimized and compared with other RNA purification-based miRNA assays, and the sensitivity was tested. Using Direct S-Poly(T) Plus method, seven potential miRNA biomarkers of colorectal cancer were validated.

Results: It is possible to detect approximately 100 miRNAs with minimal plasma inputs (20 μl) and time (~ 140 min) with this approach. The sensitivity of this method was 2.7-343-fold higher than that of the stem-loop method, and comparable with S-Poly(T) plus method. 7 validated miRNA biomarkers of colorectal cancer by Direct S-Poly(T) plus assay could discriminate colorectal cancer stage I from healthy individuals, and promised satisfactory discrimination with the area under receiver operating characteristic (ROC) curve ranging from 0.79 to 0.94 (p value < 0.001).

Conclusions: This simple and robust protocol may have strong impact on the development of specific miRNAs as biomarkers in clinic.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757382PMC
http://dx.doi.org/10.1186/s12967-019-2061-6DOI Listing

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