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Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is the sixth most common cancer worldwide with high mortality. Circulating miRNA has been demonstrated as a novel noninvasive biomarker for many tumors. This study aimed to investigate the potential of circulating miR-125b as a prognostic marker of HCC. Exosomes were e...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546809/ https://www.ncbi.nlm.nih.gov/pubmed/28814883 http://dx.doi.org/10.2147/OTT.S140062 |
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author | Liu, Weifeng Hu, Jie Zhou, Kaiqian Chen, Feiyu Wang, Zheng Liao, Boyi Dai, Zhi Cao, Ya Fan, Jia Zhou, Jian |
author_facet | Liu, Weifeng Hu, Jie Zhou, Kaiqian Chen, Feiyu Wang, Zheng Liao, Boyi Dai, Zhi Cao, Ya Fan, Jia Zhou, Jian |
author_sort | Liu, Weifeng |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is the sixth most common cancer worldwide with high mortality. Circulating miRNA has been demonstrated as a novel noninvasive biomarker for many tumors. This study aimed to investigate the potential of circulating miR-125b as a prognostic marker of HCC. Exosomes were extracted from serum samples collected from two independent cohorts: cohort 1: HCC (n=30), chronic hepatitis B (CHB, n=30), liver cirrhosis (LC, n=30); cohort 2: HCC (n=128). We found that miR-125b levels were remarkably increased in exosomes compared to those in serum from patients with CHB, LC, and HCC (P<0.01, respectively). However, miR-125b levels in exosomes and the serum from HCC patients were inferior to that of CHB (P<0.01 and P=0.06) and LC patients (P<0.01 for all). Additionally, miR-125b levels in exosomes were associated with tumor number (P=0.02), encapsulation (P<0.01), and TNM stage (P<0.01). Kaplan–Meier analysis indicated that HCC patients with lower exosomal miR-125b levels showed reduced time to recurrence (TTR) (P<0.01) and overall survival (OS) (P<0.01). Furthermore, multivariate analysis revealed that miR-125b level in exosomes, but not in serum, was an independent predictive factor for TTR (P<0.001) and OS (P=0.011). Exosomal miR-125b levels predicted the recurrence and survival of HCC patients with an area under the ROC curve of 0.739 (83.0% sensitivity and 67.9% specificity) and 0.702 (82.5% sensitivity and 53.4% specificity). In conclusion, exosomal miR-125b could serve as a promising prognostic marker for HCC. |
format | Online Article Text |
id | pubmed-5546809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55468092017-08-16 Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma Liu, Weifeng Hu, Jie Zhou, Kaiqian Chen, Feiyu Wang, Zheng Liao, Boyi Dai, Zhi Cao, Ya Fan, Jia Zhou, Jian Onco Targets Ther Original Research Hepatocellular carcinoma (HCC) is the sixth most common cancer worldwide with high mortality. Circulating miRNA has been demonstrated as a novel noninvasive biomarker for many tumors. This study aimed to investigate the potential of circulating miR-125b as a prognostic marker of HCC. Exosomes were extracted from serum samples collected from two independent cohorts: cohort 1: HCC (n=30), chronic hepatitis B (CHB, n=30), liver cirrhosis (LC, n=30); cohort 2: HCC (n=128). We found that miR-125b levels were remarkably increased in exosomes compared to those in serum from patients with CHB, LC, and HCC (P<0.01, respectively). However, miR-125b levels in exosomes and the serum from HCC patients were inferior to that of CHB (P<0.01 and P=0.06) and LC patients (P<0.01 for all). Additionally, miR-125b levels in exosomes were associated with tumor number (P=0.02), encapsulation (P<0.01), and TNM stage (P<0.01). Kaplan–Meier analysis indicated that HCC patients with lower exosomal miR-125b levels showed reduced time to recurrence (TTR) (P<0.01) and overall survival (OS) (P<0.01). Furthermore, multivariate analysis revealed that miR-125b level in exosomes, but not in serum, was an independent predictive factor for TTR (P<0.001) and OS (P=0.011). Exosomal miR-125b levels predicted the recurrence and survival of HCC patients with an area under the ROC curve of 0.739 (83.0% sensitivity and 67.9% specificity) and 0.702 (82.5% sensitivity and 53.4% specificity). In conclusion, exosomal miR-125b could serve as a promising prognostic marker for HCC. Dove Medical Press 2017-08-01 /pmc/articles/PMC5546809/ /pubmed/28814883 http://dx.doi.org/10.2147/OTT.S140062 Text en © 2017 Liu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Liu, Weifeng Hu, Jie Zhou, Kaiqian Chen, Feiyu Wang, Zheng Liao, Boyi Dai, Zhi Cao, Ya Fan, Jia Zhou, Jian Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma |
title | Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma |
title_full | Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma |
title_fullStr | Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma |
title_full_unstemmed | Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma |
title_short | Serum exosomal miR-125b is a novel prognostic marker for hepatocellular carcinoma |
title_sort | serum exosomal mir-125b is a novel prognostic marker for hepatocellular carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546809/ https://www.ncbi.nlm.nih.gov/pubmed/28814883 http://dx.doi.org/10.2147/OTT.S140062 |
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