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Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation

BACKGROUND: Predictive biomarkers for the recurrence of hepatocellular carcinoma (HCC) have great benefit in the selection of treatment options, including liver transplantation (LT), for HCC. The purpose of this study was to identify specific microRNAs (miRs) in exosomes from the serum of patients w...

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Autores principales: Sugimachi, K, Matsumura, T, Hirata, H, Uchi, R, Ueda, M, Ueo, H, Shinden, Y, Iguchi, T, Eguchi, H, Shirabe, K, Ochiya, T, Maehara, Y, Mimori, K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453648/
https://www.ncbi.nlm.nih.gov/pubmed/25584485
http://dx.doi.org/10.1038/bjc.2014.621
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author Sugimachi, K
Matsumura, T
Hirata, H
Uchi, R
Ueda, M
Ueo, H
Shinden, Y
Iguchi, T
Eguchi, H
Shirabe, K
Ochiya, T
Maehara, Y
Mimori, K
author_facet Sugimachi, K
Matsumura, T
Hirata, H
Uchi, R
Ueda, M
Ueo, H
Shinden, Y
Iguchi, T
Eguchi, H
Shirabe, K
Ochiya, T
Maehara, Y
Mimori, K
author_sort Sugimachi, K
collection PubMed
description BACKGROUND: Predictive biomarkers for the recurrence of hepatocellular carcinoma (HCC) have great benefit in the selection of treatment options, including liver transplantation (LT), for HCC. The purpose of this study was to identify specific microRNAs (miRs) in exosomes from the serum of patients with recurrent HCC and to validate these molecules as novel biomarkers for HCC recurrence. METHODS: We employed microarray-based expression profiling of miRs derived from exosomes in the serum of HCC patients to identify a biomarker that distinguishes between patients with and without HCC recurrence after LT. This was followed by the validation in a separate cohort of 59 HCC patients who underwent living related LT. The functions and potential gene targets of the recurrence-specific miRs were analysed using a database, clinical samples and HCC cell lines. RESULTS: We found that miR-718 showed significantly different expression in the serum exosomes of HCC cases with recurrence after LT compared with those without recurrence. Decreased expression of miR-718 was associated with HCC tumour aggressiveness in the validated cohort series. We identified HOXB8 as a potential target gene of miR-718, and its upregulation was associated with poor prognosis. CONCLUSION: Circulating miRs in serum exosomes have potential as novel biomarkers for predicting HCC recurrence.
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spelling pubmed-44536482016-02-03 Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation Sugimachi, K Matsumura, T Hirata, H Uchi, R Ueda, M Ueo, H Shinden, Y Iguchi, T Eguchi, H Shirabe, K Ochiya, T Maehara, Y Mimori, K Br J Cancer Molecular Diagnostics BACKGROUND: Predictive biomarkers for the recurrence of hepatocellular carcinoma (HCC) have great benefit in the selection of treatment options, including liver transplantation (LT), for HCC. The purpose of this study was to identify specific microRNAs (miRs) in exosomes from the serum of patients with recurrent HCC and to validate these molecules as novel biomarkers for HCC recurrence. METHODS: We employed microarray-based expression profiling of miRs derived from exosomes in the serum of HCC patients to identify a biomarker that distinguishes between patients with and without HCC recurrence after LT. This was followed by the validation in a separate cohort of 59 HCC patients who underwent living related LT. The functions and potential gene targets of the recurrence-specific miRs were analysed using a database, clinical samples and HCC cell lines. RESULTS: We found that miR-718 showed significantly different expression in the serum exosomes of HCC cases with recurrence after LT compared with those without recurrence. Decreased expression of miR-718 was associated with HCC tumour aggressiveness in the validated cohort series. We identified HOXB8 as a potential target gene of miR-718, and its upregulation was associated with poor prognosis. CONCLUSION: Circulating miRs in serum exosomes have potential as novel biomarkers for predicting HCC recurrence. Nature Publishing Group 2015-02-03 2015-01-13 /pmc/articles/PMC4453648/ /pubmed/25584485 http://dx.doi.org/10.1038/bjc.2014.621 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Sugimachi, K
Matsumura, T
Hirata, H
Uchi, R
Ueda, M
Ueo, H
Shinden, Y
Iguchi, T
Eguchi, H
Shirabe, K
Ochiya, T
Maehara, Y
Mimori, K
Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation
title Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation
title_full Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation
title_fullStr Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation
title_full_unstemmed Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation
title_short Identification of a bona fide microRNA biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation
title_sort identification of a bona fide microrna biomarker in serum exosomes that predicts hepatocellular carcinoma recurrence after liver transplantation
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453648/
https://www.ncbi.nlm.nih.gov/pubmed/25584485
http://dx.doi.org/10.1038/bjc.2014.621
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