Detection of let-7 miRNAs in urine supernatant as potential diagnostic approach in non-metastatic clear-cell renal cell carcinoma
Jazyk angličtina Země Chorvatsko Médium print
Typ dokumentu časopisecké články
PubMed
28694731
PubMed Central
PMC5493171
DOI
10.11613/bm.2017.043
PII: bm-27-411
Knihovny.cz E-zdroje
- Klíčová slova
- diagnostic biomarker, let-7, renal cell carcinoma, urine microRNAs,
- MeSH
- dospělí MeSH
- karcinom z renálních buněk diagnóza genetika moč MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikro RNA genetika moč MeSH
- nádorové biomarkery genetika MeSH
- nádory ledvin diagnóza genetika moč MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- regulace genové exprese u nádorů * MeSH
- ROC křivka MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- mikro RNA MeSH
- mirnlet7 microRNA, human MeSH Prohlížeč
- nádorové biomarkery MeSH
INTRODUCTION: Urinary microRNAs (miRNAs) are emerging as a clinically useful tool for early and non-invasive detection of various types of cancer. The aim of this study was to evaluate whether let-7 family miRNAs differ in their urinary concentrations between renal cell carcinoma (RCC) cases and healthy controls. MATERIALS AND METHODS: In the case-control study, 69 non-metastatic clear-cell RCC patients and 36 gender/age-matched healthy controls were prospectively enrolled. Total RNA was purified from cell-free supernatant of the 105 first morning urine specimens. Let-7 family miRNAs were determined in cell-free supernatant using quantitative miRNA real-time reverse-transcription PCR and absolute quantification approach. RESULTS: Concentrations of all let-7 miRNAs (let-7a, let-7b, let-7c, let-7d, let-7e and let-7g) were significantly higher in urine samples obtained from RCC patients compared to healthy controls (P < 0.001; P < 0.001; P = 0.005; P = 0.006; P = 0.015 and P = 0.002, respectively). Subsequent ROC analysis has shown that let-7a concentration possesses good ability to differentiate between cases and controls with area under curve being 0.8307 (sensitivity 71%, specificity 81%). CONCLUSIONS: We have shown that let-7 miRNAs are abundant in the urine samples of patients with clear-cell RCC, and out of six let-7 family members, let-7a outperforms the others and presents promising non-invasive biomarker for the detection of RCC.
Department of Urology University Hospital Brno and Masaryk University Brno Brno Czech Republic
Masaryk Memorial Cancer Institute Department of Comprehensive Cancer Care Brno Czech Republic
Masaryk Memorial Cancer Institute Department of Urologic Oncology Brno Czech Republic
Masaryk University Central European Institute of Technology Brno Czech Republic
Zobrazit více v PubMed
Howlader N, Noone AM, Krapcho M, Miller D, Bishop K, Altekruse SF, et al. SEER Cancer Statistics Review, 1975-2012. In: Bethesda, MD: National Cancer Institute; 2015. Available at: http://seer.cancer.gov/csr/1975_2012. Accessed March 3rd 2016.
Fedorko M, Pacik D, Wasserbauer R, Juracek J, Varga G, Ghazal M, et al. MicroRNAs in the pathogenesis of renal cell carcinoma and their diagnostic and prognostic utility as cancer biomarkers. Int J Biol Markers. 2016;31:e26–37. 10.5301/jbm.5000174 PubMed DOI
Mlcochova H, Hezova R, Stanik M, Slaby O. Urine microRNAs as potential noninvasive biomarkers in urologic cancers. Urol Oncol. 2014;32:41.e1–9. 10.1016/j.urolonc.2013.04.011 PubMed DOI
Barh D, Malhotra R, Ravi B, Sindhurani P. MicroRNA let-7: an emerging next-generation cancer therapeutic. Curr Oncol. 2010;17:70–80. 10.3747/co.v17i1.356 PubMed DOI PMC
Liu Y, Yin BD, Zhang CC, Zhou LB, Fan J. Hsa-let-7a functions as a tumor suppressor in renal cell carcinoma cell lines by targeting c-myc. Biochem Biophys Res Commun. 2012;417:371–5. 10.1016/j.bbrc.2011.11.119 PubMed DOI
Boyerinas B, Park S, Hau A, Murmann A, Peter M. The role of let-7 in cell differentiation and cancer. Endocr Relat Cancer. 2010;17:F19–36. 10.1677/ERC-09-0184 PubMed DOI
Liu Q, Shin Y, Kee JS, Kim KW, Rafei SR, Perera AP, et al. Mach-Zehnder interferometer (MZI) point-of-care system for rapid multiplexed detection of microRNAs in human urine specimens. Biosens Bioelectron. 2015;71:365–72. 10.1016/j.bios.2015.04.052 PubMed DOI
Ben-Dov IZ, Tan YC, Morozov P, Wilson PD, Rennert H, Blumenfeld JD, Tuchl T. Urine microRNA as potential biomarkers of autosomal dominant polycystic kidney disease progression: description of miRNA profiles at baseline. PLoS One. 2014. Jan 29;9(1):e86856. 10.1371/journal.pone.0086856 PubMed DOI PMC
Hong Y, Wang C, Fu Z, Liang H, Zhang S, Lu M, et al. Systematic characterization of seminal plasma piRNAs as molecular biomarkers for male infertility. Sci Rep. 2016;6:24229. 10.1038/srep24229 PubMed DOI PMC
von Brandenstein M, Pandarakalam JJ, Kroon L, Loeser H, Herden J, Braun G, et al. MicroRNA 15a, inversely correlated to PKCα, is a potential marker to differentiate between benign and malignant renal tumors in biopsy and urine samples. Am J Pathol. 2012;180:1787–97. 10.1016/j.ajpath.2012.01.014 PubMed DOI
Li G, Zhao A, Péoch M, Cottier M, Mottet N. Detection of urinary cell-free miR-210 as a potential tool of liquid biopsy for clear cell renal cell carcinoma. Urol Oncol. 2017;35:294–9. 10.1016/j.urolonc.2016.12.007 PubMed DOI
The Effect of Tobacco Smoking and Smoking Cessation on Urinal miRNAs in a Pilot Study