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Prognostic Value of Tumor Tissue Up-regulated microRNAs in Clear Cell Renal Cell Carcinoma (ccRCC)
M. Pesta, I. Travnicek, V. Kulda, P. Ostasov, J. Windrichova, K. Houfkova, T. Knizkova, B. Bendova, O. Hes, M. Hora, O. Topolcan, J. Polivka
Language English Country Greece
Document type Journal Article
NLK
PubMed Central
from 2017
Europe PubMed Central
from 2017
Open Access Digital Library
from 2004-01-01
PubMed
38936941
DOI
10.21873/invivo.13631
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Kaplan-Meier Estimate MeSH
- Carcinoma, Renal Cell * genetics pathology mortality metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- MicroRNAs * genetics MeSH
- Biomarkers, Tumor * genetics MeSH
- Kidney Neoplasms * genetics pathology mortality metabolism MeSH
- Prognosis MeSH
- Gene Expression Regulation, Neoplastic * MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Neoplasm Staging MeSH
- Gene Expression Profiling * MeSH
- Up-Regulation MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND/AIM: The management of patients with clear cell renal cell carcinoma (ccRCC) includes prognosis assessment based on TNM classification and biochemical markers. This approach stratifies patients with advanced ccRCC into groups of favorable, intermediate, and poor prognosis. The aim of the study was to improve prognosis estimation using microRNAs involved in the pathogenesis of ccRCC. PATIENTS AND METHODS: The study was based on a histologically-verified set of matched ccRCC FFPE tissue samples (normal renal tissue, primary tumor, metastasis, n=20+20+20). The expression of 2,549 microRNAs was analyzed using the SurePrint G3 Human miRNA microarray kit (Agilent Technologies). Prognostic value of significantly deregulated microRNAs was further evaluated on microRNA expression and clinical data of 475 patients obtained from TCGA Kidney Clear Cell Carcinoma (KIRC) database. RESULTS: There were 13 up-regulated and 6 down-regulated microRNAs in tumor tissues compared to control tissues. Among them, survival analysis revealed those with prognostic significance. Patients with high expression of miR-21, miR-27a, miR-34a, miR-106b, miR-210, and miR-342 showed significantly unfavorable outcome. The opposite was observed for miR-30e, patients with low expression had significantly shorter survival. CONCLUSION: The inclusion of these microRNAs in a prognostic panel holds the potential to enhance stratification scoring systems, on which the treatment of ccRCC patients is based.
Biomedical Center Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Department of Biology Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Department of Pathology University Hospital in Pilsen Pilsen Czech Republic
Department of Urology University Hospital in Pilsen Pilsen Czech Republic
Laboratory of Immunoanalysis University Hospital in Pilsen Pilsen Czech Republic
References provided by Crossref.org
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