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Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy

BACKGROUND: MicroRNAs are endogenously expressed regulatory noncoding RNAs. Previous studies have shown altered expression levels of several microRNAs in renal cell carcinoma. METHODS: We examined the expression levels of selected microRNAs in 38 samples of conventional renal cell carcinoma (RCC) an...

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Autores principales: Slaby, Ondrej, Jancovicova, Jana, Lakomy, Radek, Svoboda, Marek, Poprach, Alexandr, Fabian, Pavel, Kren, Leos, Michalek, Jaroslav, Vyzula, Rostislav
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907341/
https://www.ncbi.nlm.nih.gov/pubmed/20609231
http://dx.doi.org/10.1186/1756-9966-29-90
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author Slaby, Ondrej
Jancovicova, Jana
Lakomy, Radek
Svoboda, Marek
Poprach, Alexandr
Fabian, Pavel
Kren, Leos
Michalek, Jaroslav
Vyzula, Rostislav
author_facet Slaby, Ondrej
Jancovicova, Jana
Lakomy, Radek
Svoboda, Marek
Poprach, Alexandr
Fabian, Pavel
Kren, Leos
Michalek, Jaroslav
Vyzula, Rostislav
author_sort Slaby, Ondrej
collection PubMed
description BACKGROUND: MicroRNAs are endogenously expressed regulatory noncoding RNAs. Previous studies have shown altered expression levels of several microRNAs in renal cell carcinoma. METHODS: We examined the expression levels of selected microRNAs in 38 samples of conventional renal cell carcinoma (RCC) and 10 samples of non-tumoral renal parenchyma using TaqMan real-time PCR method. RESULTS: The expression levels of miRNA-155 (p < 0.0001), miRNA-210 (p < 0.0001), miRNA-106a (p < 0.0001) and miRNA-106b (p < 0.0001) were significantly over-expressed in tumor tissue, whereas the expression of miRNA-141 (p < 0.0001) and miRNA-200c (p < 0.0001) were significantly decreased in RCC samples. There were no significant differences between expression levels of miRNA-182 and miRNA-200b in tumor samples and renal parenchyma. Our data suggest that expression levels of miRNA-106b are significantly lower in tumors of patients who developed metastasis (p = 0.030) and miR-106b is a potential predictive marker of early metastasis after nephrectomy in RCC patients (long-rank p = 0.032). CONCLUSIONS: We have confirmed previous observations obtained by miRNA microarray analysis using standardized real-time PCR method. For the first time, we have identified a prognostic significance of miRNA-106b, which, after validation on a larger group of patients, maybe useful as a promising biomarker in patients with RCC.
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spelling pubmed-29073412010-07-21 Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy Slaby, Ondrej Jancovicova, Jana Lakomy, Radek Svoboda, Marek Poprach, Alexandr Fabian, Pavel Kren, Leos Michalek, Jaroslav Vyzula, Rostislav J Exp Clin Cancer Res Research BACKGROUND: MicroRNAs are endogenously expressed regulatory noncoding RNAs. Previous studies have shown altered expression levels of several microRNAs in renal cell carcinoma. METHODS: We examined the expression levels of selected microRNAs in 38 samples of conventional renal cell carcinoma (RCC) and 10 samples of non-tumoral renal parenchyma using TaqMan real-time PCR method. RESULTS: The expression levels of miRNA-155 (p < 0.0001), miRNA-210 (p < 0.0001), miRNA-106a (p < 0.0001) and miRNA-106b (p < 0.0001) were significantly over-expressed in tumor tissue, whereas the expression of miRNA-141 (p < 0.0001) and miRNA-200c (p < 0.0001) were significantly decreased in RCC samples. There were no significant differences between expression levels of miRNA-182 and miRNA-200b in tumor samples and renal parenchyma. Our data suggest that expression levels of miRNA-106b are significantly lower in tumors of patients who developed metastasis (p = 0.030) and miR-106b is a potential predictive marker of early metastasis after nephrectomy in RCC patients (long-rank p = 0.032). CONCLUSIONS: We have confirmed previous observations obtained by miRNA microarray analysis using standardized real-time PCR method. For the first time, we have identified a prognostic significance of miRNA-106b, which, after validation on a larger group of patients, maybe useful as a promising biomarker in patients with RCC. BioMed Central 2010-07-07 /pmc/articles/PMC2907341/ /pubmed/20609231 http://dx.doi.org/10.1186/1756-9966-29-90 Text en Copyright ©2010 Slaby et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Slaby, Ondrej
Jancovicova, Jana
Lakomy, Radek
Svoboda, Marek
Poprach, Alexandr
Fabian, Pavel
Kren, Leos
Michalek, Jaroslav
Vyzula, Rostislav
Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
title Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
title_full Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
title_fullStr Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
title_full_unstemmed Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
title_short Expression of miRNA-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
title_sort expression of mirna-106b in conventional renal cell carcinoma is a potential marker for prediction of early metastasis after nephrectomy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907341/
https://www.ncbi.nlm.nih.gov/pubmed/20609231
http://dx.doi.org/10.1186/1756-9966-29-90
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