Document Type: Research Articles
Department of Biomedical Sciences, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Department of Pathology, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
MicroRNAs (miRNAs) are small, non-coding RNA molecules that regulate gene expression at the post-transcriptional
level. Since aberrant expression of miRNAs has been proposed as usage for blood-based biomarkers, hence reliable
techniques for miRNA isolation as well as stability of miRNAs in various stored conditions needs to be explored. This
present study aimed to investigate the efficacy of the Trizol-based isolation technique and the stability of miRNAs in
stored serum and cDNA derivatives. Total RNA, including miRNAs, was isolated from human serum and a comparison
of the efficiency of the Trizol®LS reagent isolation method against the miRNeasy®mini kit was conducted. Expression
of RNU6, miR-145, and miR-20a was determined by quantitative real-time polymerase chain reaction (qRT-PCR).
We showed that Trizol®LS isolation yielded significantly lower RNA concentrations than that of the miRNeasy®mini
kit by approximately 35%. Purity of the isolated RNAs by both methods was similar. RNU6, miR-145, and miR-20a
degraded at room temperature, but all genes were stable at 4ºC, -20ºC and -80ºC for a 72-hrs period, in both serum and
cDNA storage conditions. In the stored cDNA derivatives, we observed the stability of RNU6, miR-145, and miR-20a
for 3 months at -20ºC, and all genes also resisted 4 repeated freeze-thaw cycles at -20ºC. In conclusion, the Trizol-based
method is efficient as well as economical to use for quantification of circulating miRNAs. In addition, we proposed
that the storage of miRNA-derived cDNAs may be an alternative choice to avoid the stability effect.