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Prognostic value of circulating microRNAs in upper tract urinary carcinoma

The identification of upper tract urinary carcinoma (UTUC) prognostic biomarkers is urgently needed to predict tumour progression. This study aimed to identify serum microRNAs (miRNAs) that may be useful as minimally invasive predictive biomarkers of tumour progression and survival in UTUC patients....

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Autores principales: Montalbo, Ruth, Izquierdo, Laura, Ingelmo-Torres, Mercedes, Lozano, Juan José, Capitán, David, Alcaraz, Antonio, Mengual, Lourdes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908279/
https://www.ncbi.nlm.nih.gov/pubmed/29682178
http://dx.doi.org/10.18632/oncotarget.24672
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author Montalbo, Ruth
Izquierdo, Laura
Ingelmo-Torres, Mercedes
Lozano, Juan José
Capitán, David
Alcaraz, Antonio
Mengual, Lourdes
author_facet Montalbo, Ruth
Izquierdo, Laura
Ingelmo-Torres, Mercedes
Lozano, Juan José
Capitán, David
Alcaraz, Antonio
Mengual, Lourdes
author_sort Montalbo, Ruth
collection PubMed
description The identification of upper tract urinary carcinoma (UTUC) prognostic biomarkers is urgently needed to predict tumour progression. This study aimed to identify serum microRNAs (miRNAs) that may be useful as minimally invasive predictive biomarkers of tumour progression and survival in UTUC patients. To this end, 33 UTUC patients who underwent radical nephroureterectomy at the Hospital Clinic of Barcelona were prospectively included. Expression of 800 miRNAs was evaluated in serum samples from these patients using nCounter® miRNA Expression Assays. The study was divided into an initial discovery phase (n=12) and a validation phase (n=21). Cox regression analysis was used for survival analysis. The median follow-up (range) of the series was 42 months (9-100 months). In the discovery phase, 38 differentially expressed miRNAs were identified between progressing and non-progressing UTUC patients (p<0.05). Validation of these 38 miRNAs in an independent set of UTUC patients confirmed the differential expression in 18 of them (p<0.05). Cox Regression analysis showed miR-151b and pathological stage as significant prognostic factors for tumour progression (HR=0.33, p<0.001 and HR=2.62, p=0.006, respectively) and cancer specific survival (HR=0.25, p<0.001 and HR=3.98, p=0.003, respectively). Survival curves revealed that miR-151b is able to discriminate between two groups of UTUC patients with a highly significant different probability of tumour progression (p=0.006) and cancer specific survival (p=0.034). Although the data needs to be externally validated, miRNA analysis in serum appears to be a valuable prognostic tool in UTUC patients. Particularly, differential expression of miR-151b in serum may serve as a minimally invasive prognostic tool in UTUC.
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spelling pubmed-59082792018-04-20 Prognostic value of circulating microRNAs in upper tract urinary carcinoma Montalbo, Ruth Izquierdo, Laura Ingelmo-Torres, Mercedes Lozano, Juan José Capitán, David Alcaraz, Antonio Mengual, Lourdes Oncotarget Research Paper The identification of upper tract urinary carcinoma (UTUC) prognostic biomarkers is urgently needed to predict tumour progression. This study aimed to identify serum microRNAs (miRNAs) that may be useful as minimally invasive predictive biomarkers of tumour progression and survival in UTUC patients. To this end, 33 UTUC patients who underwent radical nephroureterectomy at the Hospital Clinic of Barcelona were prospectively included. Expression of 800 miRNAs was evaluated in serum samples from these patients using nCounter® miRNA Expression Assays. The study was divided into an initial discovery phase (n=12) and a validation phase (n=21). Cox regression analysis was used for survival analysis. The median follow-up (range) of the series was 42 months (9-100 months). In the discovery phase, 38 differentially expressed miRNAs were identified between progressing and non-progressing UTUC patients (p<0.05). Validation of these 38 miRNAs in an independent set of UTUC patients confirmed the differential expression in 18 of them (p<0.05). Cox Regression analysis showed miR-151b and pathological stage as significant prognostic factors for tumour progression (HR=0.33, p<0.001 and HR=2.62, p=0.006, respectively) and cancer specific survival (HR=0.25, p<0.001 and HR=3.98, p=0.003, respectively). Survival curves revealed that miR-151b is able to discriminate between two groups of UTUC patients with a highly significant different probability of tumour progression (p=0.006) and cancer specific survival (p=0.034). Although the data needs to be externally validated, miRNA analysis in serum appears to be a valuable prognostic tool in UTUC patients. Particularly, differential expression of miR-151b in serum may serve as a minimally invasive prognostic tool in UTUC. Impact Journals LLC 2018-03-30 /pmc/articles/PMC5908279/ /pubmed/29682178 http://dx.doi.org/10.18632/oncotarget.24672 Text en Copyright: © 2018 Montalbo et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Montalbo, Ruth
Izquierdo, Laura
Ingelmo-Torres, Mercedes
Lozano, Juan José
Capitán, David
Alcaraz, Antonio
Mengual, Lourdes
Prognostic value of circulating microRNAs in upper tract urinary carcinoma
title Prognostic value of circulating microRNAs in upper tract urinary carcinoma
title_full Prognostic value of circulating microRNAs in upper tract urinary carcinoma
title_fullStr Prognostic value of circulating microRNAs in upper tract urinary carcinoma
title_full_unstemmed Prognostic value of circulating microRNAs in upper tract urinary carcinoma
title_short Prognostic value of circulating microRNAs in upper tract urinary carcinoma
title_sort prognostic value of circulating micrornas in upper tract urinary carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908279/
https://www.ncbi.nlm.nih.gov/pubmed/29682178
http://dx.doi.org/10.18632/oncotarget.24672
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