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ABSTRACT: Background
MicroRNAs circulating in the blood, stabilized by complexation with proteins and/or additionally by encapsulation in lipid vesicles, are currently being evaluated as biomarkers. The consequences of their differential association with lipids/vesicles for their stability and use as biomarkers are largely unexplored and are subject of the present study.Methods
The levels of a set of selected microRNAs were determined by quantitative reverse-transcription PCR after extraction from sera or vesicle- and non-vesicle fractions prepared from sera. The stability of these microRNAs after incubation with RNase A or RNase inhibitor, an inhibitor of RNase A family enzymes was studied.Results
The levels of microRNA-1 and microRNA-122, but not those of microRNA-16, micro
SUBMITTER: Koberle V
PROVIDER: S-EPMC3779196 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature