Circulating miRNAs miR-34a and miR-150 associated with colorectal cancer progression
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25924769
PubMed Central
PMC4417244
DOI
10.1186/s12885-015-1327-5
PII: 10.1186/s12885-015-1327-5
Knihovny.cz E-zdroje
- MeSH
- adenom krev patologie MeSH
- časná detekce nádoru MeSH
- diferenciální diagnóza * MeSH
- kolorektální nádory krev genetika patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mikro RNA krev genetika MeSH
- nádorové biomarkery biosyntéza genetika MeSH
- polypy tlustého střeva krev patologie MeSH
- progrese nemoci MeSH
- regulace genové exprese u nádorů MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- mikro RNA MeSH
- MIRN150 microRNA, human MeSH Prohlížeč
- MIRN34 microRNA, human MeSH Prohlížeč
- nádorové biomarkery MeSH
BACKGROUND: Screening for the early detection of colorectal cancer is important to improve patient survival. The aim of this study was to investigate the potential of circulating cell-free miRNAs as biomarkers of CRC, and their efficiency at delineating patients with polyps and benign adenomas from normal and cancer patient groups. METHODS: The expression of 667 miRNAs was assessed in a discovery set of 48 plasma samples comprising normal, polyp, adenoma, and early and advanced cancer samples. Three miRNAs (miR-34a, miR-150, and miR-923) were further examined in a validation cohort of 97 subjects divided into the same five groups, and in an independent public dataset of 40 CRC samples and paired normal tissues. RESULTS: High levels of circulating miR-34a and low miR-150 levels distinguished groups of patients with polyps from those with advanced cancer (AUC = 0.904), and low circulating miR-150 levels separated patients with adenomas from those with advanced cancer (AUC = 0.875). In addition, the altered expression of miR-34a and miR-150 in an independent public dataset of forty CRC samples and paired normal tissues was confirmed. CONCLUSION: We identified two circulating miRNAs capable of distinguishing patient groups with different diseases of the colon from each other, and patients with advanced cancer from benign disease groups.
1st Medical Faculty of Charles University and Thomayer Hospital Prague Czech Republic
Department of Biology Maynooth University Maynooth Co Maynooth Co Kildare Ireland
Department of Colorectal Surgery AMNCH Hospital Dublin 24 Ireland
Human Genetics Foundation Turin Italy
Institute of Experimental Medicine Academy of Sciences of the Czech Republic Prague Czech Republic
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