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Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma

BACKGROUND: There is no standard serum biomarker used for diagnosis or early detection of recurrence for renal cell carcinoma (RCC) patients. MicroRNAs (miRNAs) are abundant and highly stable in blood serum, and have been recently described as powerful circulating biomarkers in a wide range of solid...

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Autores principales: Redova, Martina, Poprach, Alexandr, Nekvindova, Jana, Iliev, Robert, Radova, Lenka, Lakomy, Radek, Svoboda, Marek, Vyzula, Rostislav, Slaby, Ondrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340316/
https://www.ncbi.nlm.nih.gov/pubmed/22440013
http://dx.doi.org/10.1186/1479-5876-10-55
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author Redova, Martina
Poprach, Alexandr
Nekvindova, Jana
Iliev, Robert
Radova, Lenka
Lakomy, Radek
Svoboda, Marek
Vyzula, Rostislav
Slaby, Ondrej
author_facet Redova, Martina
Poprach, Alexandr
Nekvindova, Jana
Iliev, Robert
Radova, Lenka
Lakomy, Radek
Svoboda, Marek
Vyzula, Rostislav
Slaby, Ondrej
author_sort Redova, Martina
collection PubMed
description BACKGROUND: There is no standard serum biomarker used for diagnosis or early detection of recurrence for renal cell carcinoma (RCC) patients. MicroRNAs (miRNAs) are abundant and highly stable in blood serum, and have been recently described as powerful circulating biomarkers in a wide range of solid cancers. Our aim was to identify miRNA signature that can distinguish the blood serum of RCC patients and matched healthy controls and validate identified miRNAs as potential biomarkers for RCC. METHODS: In the screening phase of the study, blood serum of 15 RCC patients and 12 matched healthy controls were analyzed by use of the TaqMan Low-Density Arrays enabling parallel identification of expression levels of 667 miRNAs through qRT-PCR-based approach. In the validation phase, identified miRNAs were further evaluated on the independent group of 90 RCC patients and 35 matched healthy controls by use of individual qRT-PCR assays and statistically evaluated. RESULTS: We identified 30 miRNAs differentially expressed between serum of RCC patients and healthy controls: 19 miRNAs were up-regulated and 11 miRNAs were down-regulated in RCC patients. MiR-378, miR-451 and miR-150 were further evaluated in the independent group of patients, and two of them were successfully validated: levels of miR-378 were increased (p = 0.0003, AUC = 0.71), miR-451 levels were decreased (p < 0.0001, AUC = 0.77) in serum of RCC patients. Combination of miR-378 and miR-451 enable identification of RCC serum with the sensitivity of 81%, specificity 83% and AUC = 0.86. CONCLUSIONS: Circulating miRNAs in serum are promising biomarkers in RCC.
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spelling pubmed-33403162012-05-01 Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma Redova, Martina Poprach, Alexandr Nekvindova, Jana Iliev, Robert Radova, Lenka Lakomy, Radek Svoboda, Marek Vyzula, Rostislav Slaby, Ondrej J Transl Med Research BACKGROUND: There is no standard serum biomarker used for diagnosis or early detection of recurrence for renal cell carcinoma (RCC) patients. MicroRNAs (miRNAs) are abundant and highly stable in blood serum, and have been recently described as powerful circulating biomarkers in a wide range of solid cancers. Our aim was to identify miRNA signature that can distinguish the blood serum of RCC patients and matched healthy controls and validate identified miRNAs as potential biomarkers for RCC. METHODS: In the screening phase of the study, blood serum of 15 RCC patients and 12 matched healthy controls were analyzed by use of the TaqMan Low-Density Arrays enabling parallel identification of expression levels of 667 miRNAs through qRT-PCR-based approach. In the validation phase, identified miRNAs were further evaluated on the independent group of 90 RCC patients and 35 matched healthy controls by use of individual qRT-PCR assays and statistically evaluated. RESULTS: We identified 30 miRNAs differentially expressed between serum of RCC patients and healthy controls: 19 miRNAs were up-regulated and 11 miRNAs were down-regulated in RCC patients. MiR-378, miR-451 and miR-150 were further evaluated in the independent group of patients, and two of them were successfully validated: levels of miR-378 were increased (p = 0.0003, AUC = 0.71), miR-451 levels were decreased (p < 0.0001, AUC = 0.77) in serum of RCC patients. Combination of miR-378 and miR-451 enable identification of RCC serum with the sensitivity of 81%, specificity 83% and AUC = 0.86. CONCLUSIONS: Circulating miRNAs in serum are promising biomarkers in RCC. BioMed Central 2012-03-22 /pmc/articles/PMC3340316/ /pubmed/22440013 http://dx.doi.org/10.1186/1479-5876-10-55 Text en Copyright ©2012 Redova 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
Redova, Martina
Poprach, Alexandr
Nekvindova, Jana
Iliev, Robert
Radova, Lenka
Lakomy, Radek
Svoboda, Marek
Vyzula, Rostislav
Slaby, Ondrej
Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma
title Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma
title_full Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma
title_fullStr Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma
title_full_unstemmed Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma
title_short Circulating miR-378 and miR-451 in serum are potential biomarkers for renal cell carcinoma
title_sort circulating mir-378 and mir-451 in serum are potential biomarkers for renal cell carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340316/
https://www.ncbi.nlm.nih.gov/pubmed/22440013
http://dx.doi.org/10.1186/1479-5876-10-55
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