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Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma
Recent studies have shown that circulating microRNAs are a potential biomarker in various types of malignancies. The aim of this study was to investigate the feasibility of using serum exosomal microRNAs as novel serological biomarkers for hepatocellular carcinoma (HCC) in patients with chronic hepa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650928/ https://www.ncbi.nlm.nih.gov/pubmed/26380927 http://dx.doi.org/10.1038/emm.2015.68 |
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author | Sohn, Won Kim, Jonghwa Kang, So Hee Yang, Se Ra Cho, Ju-Yeon Cho, Hyun Chin Shim, Sang Goon Paik, Yong-Han |
author_facet | Sohn, Won Kim, Jonghwa Kang, So Hee Yang, Se Ra Cho, Ju-Yeon Cho, Hyun Chin Shim, Sang Goon Paik, Yong-Han |
author_sort | Sohn, Won |
collection | PubMed |
description | Recent studies have shown that circulating microRNAs are a potential biomarker in various types of malignancies. The aim of this study was to investigate the feasibility of using serum exosomal microRNAs as novel serological biomarkers for hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). We measured the serum exosomal microRNAs and serum circulating microRNAs in patients with CHB (n=20), liver cirrhosis (LC) (n=20) and HCC (n=20). Serum exosomal microRNA was extracted from 500 μl of serum using an Exosome RNA Isolation kit. The expression levels of microRNAs were quantified by real-time PCR. The expression levels of selected microRNAs were normalized to Caenorhabditis elegans microRNA (Cel-miR-39). The serum levels of exosomal miR-18a, miR-221, miR-222 and miR-224 were significantly higher in patients with HCC than those with CHB or LC (P<0.05). Further, the serum levels of exosomal miR-101, miR-106b, miR-122 and miR-195 were lower in patients with HCC than in patients with CHB (P=0.014, P<0.001, P<0.001 and P<0.001, respectively). There was no significant difference in the levels of miR-21 and miR-93 among the three groups. Additionally, the serum levels of circulating microRNAs showed a smaller difference between HCC and either CHB or LC. This study suggests that serum exosomal microRNAs may be used as novel serological biomarkers for HCC. |
format | Online Article Text |
id | pubmed-4650928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46509282015-11-27 Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma Sohn, Won Kim, Jonghwa Kang, So Hee Yang, Se Ra Cho, Ju-Yeon Cho, Hyun Chin Shim, Sang Goon Paik, Yong-Han Exp Mol Med Original Article Recent studies have shown that circulating microRNAs are a potential biomarker in various types of malignancies. The aim of this study was to investigate the feasibility of using serum exosomal microRNAs as novel serological biomarkers for hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). We measured the serum exosomal microRNAs and serum circulating microRNAs in patients with CHB (n=20), liver cirrhosis (LC) (n=20) and HCC (n=20). Serum exosomal microRNA was extracted from 500 μl of serum using an Exosome RNA Isolation kit. The expression levels of microRNAs were quantified by real-time PCR. The expression levels of selected microRNAs were normalized to Caenorhabditis elegans microRNA (Cel-miR-39). The serum levels of exosomal miR-18a, miR-221, miR-222 and miR-224 were significantly higher in patients with HCC than those with CHB or LC (P<0.05). Further, the serum levels of exosomal miR-101, miR-106b, miR-122 and miR-195 were lower in patients with HCC than in patients with CHB (P=0.014, P<0.001, P<0.001 and P<0.001, respectively). There was no significant difference in the levels of miR-21 and miR-93 among the three groups. Additionally, the serum levels of circulating microRNAs showed a smaller difference between HCC and either CHB or LC. This study suggests that serum exosomal microRNAs may be used as novel serological biomarkers for HCC. Nature Publishing Group 2015-09 2015-09-18 /pmc/articles/PMC4650928/ /pubmed/26380927 http://dx.doi.org/10.1038/emm.2015.68 Text en Copyright © 2015 KSBMB. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article Sohn, Won Kim, Jonghwa Kang, So Hee Yang, Se Ra Cho, Ju-Yeon Cho, Hyun Chin Shim, Sang Goon Paik, Yong-Han Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma |
title | Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma |
title_full | Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma |
title_fullStr | Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma |
title_full_unstemmed | Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma |
title_short | Serum exosomal microRNAs as novel biomarkers for hepatocellular carcinoma |
title_sort | serum exosomal micrornas as novel biomarkers for hepatocellular carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650928/ https://www.ncbi.nlm.nih.gov/pubmed/26380927 http://dx.doi.org/10.1038/emm.2015.68 |
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