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Cell-Free Urinary MicroRNAs Expression in Small-Scale Experiments
L. Zavesky, E. Jandakova, R. Turyna, D. Duskova, L. Langmeierova, V. Weinberger, L. Minar, A. Horinek, M. Kohoutova,
Language English Country United States
Document type Journal Article
- MeSH
- Urinalysis methods MeSH
- Circulating MicroRNA genetics isolation & purification urine MeSH
- Real-Time Polymerase Chain Reaction methods MeSH
- Humans MeSH
- Endometrial Neoplasms genetics urine MeSH
- Ovarian Neoplasms genetics urine MeSH
- Reverse Transcriptase Polymerase Chain Reaction methods MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Gene Expression Profiling methods MeSH
- Check Tag
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
Cell-free microRNAs (miRNAs) have become one of the novel promising diagnostic and prognostic biomarkers for various diseases recently. Blood serum and plasma along with urine are the most common sources of clinically well, almost noninvasively available samples containing various types of miRNAs. Here, we present a protocol for a small-scale study investigating expression of several candidate miRNAs. Small-scale experiments may be worth investigating in cases where no information is available on miRNAs expression in particular diseases, for validation of previously published miRNAs with promising diagnostic potential, particularly in situations where follow-up study is aimed at validating miRNAs coming from array or NGS experiments, or where funding for these large-scale experiments is not available.Using urine miRNAs expression as the novel diagnostic tools is challenging and currently this approach is still in its infancy. Therefore, various methods may result in different conclusions depending on clinical sample sets and differences among methods used for the miRNAs isolation and quantitation. In this protocol, we present the method evaluated in the study focused on cell-free urinary miRNAs in ovarian and endometrial cancers. We recommend using stabilization tubes for the urine collection, as this step may be necessary to stop activity of RNases. Further, routine real-time PCR methods are described. We demonstrate that assessment of urinary miRNAs expression may reveal as a feasible method to explore the potential for finding novel diagnostic and prognostic markers.
Department of Obstetrics and Gynaecology University Hospital Brno Brno Czech Republic
Faculty Transfusion Centre General University Hospital Prague Prague Czech Republic
Institute for the Care of Mother and Child Prague Czech Republic
Institute of Pathology University Hospital Brno Brno Czech Republic
References provided by Crossref.org
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