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COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients

Analysis of exosomes derived from plasma or cerebrospinal fluid (CSF) has emerged as a promising biomarker platform for therapeutic monitoring in glioblastoma patients. However, the contents of the various subpopulations of exosomes in these clinical specimens remain poorly defined. Here we characte...

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Autores principales: Yamashita, Daisuke, Suehiro, Satoshi, Ohtsuka, Yoshihiro, Ozaki, Saya, Nishikawa, Masahiro, Inoue, Akihiro, Kohno, Shohei, Ohue, Shiro, Ohnishi, Takanori, Kunieda, Takeharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648223/
http://dx.doi.org/10.1093/noajnl/vdab159.111
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author Yamashita, Daisuke
Suehiro, Satoshi
Ohtsuka, Yoshihiro
Ozaki, Saya
Nishikawa, Masahiro
Inoue, Akihiro
Kohno, Shohei
Ohue, Shiro
Ohnishi, Takanori
Kunieda, Takeharu
author_facet Yamashita, Daisuke
Suehiro, Satoshi
Ohtsuka, Yoshihiro
Ozaki, Saya
Nishikawa, Masahiro
Inoue, Akihiro
Kohno, Shohei
Ohue, Shiro
Ohnishi, Takanori
Kunieda, Takeharu
author_sort Yamashita, Daisuke
collection PubMed
description Analysis of exosomes derived from plasma or cerebrospinal fluid (CSF) has emerged as a promising biomarker platform for therapeutic monitoring in glioblastoma patients. However, the contents of the various subpopulations of exosomes in these clinical specimens remain poorly defined. Here we characterize the relative abundance of miRNA species in exosomes derived from the plasma and CSF of glioblastoma patients. To this end, we first employed miRNA arrays to measure the expression of exosomal miRNAs in the plasma from glioblastoma patients (n = 24) and healthy volunteers (n = 7) as control. In addition, we performed global miRNA profiling of exosomal miRNAs in the CSF from glioblastoma patients (n = 5) and non-tumoral patients (n = 3; hydrocephalus patients) as control. In plasma derived exosomes, 80 miRNAs were altered by >2-fold in glioblastoma patients compared to controls. In CSF, 92 miRNAs were altered by >2-fold in glioblastoma patients compared to controls. Combined analysis of plasma and CSF revealed a similar fold difference in eight miRNAs. Next, we measured these eight miRNAs expression in in the plasma from pre- and post-operative glioblastoma patients (n = 9). Among these eight miRNAs, we identified only one miRNA (miR-34b-3p) that was upregulated in exosomes from pre-operative glioblastoma patients. Our results suggest that miR-34b-3p might have a potential as a novel diagnostic marker or a therapeutic tool for glioblastoma patients.
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spelling pubmed-86482232021-12-07 COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients Yamashita, Daisuke Suehiro, Satoshi Ohtsuka, Yoshihiro Ozaki, Saya Nishikawa, Masahiro Inoue, Akihiro Kohno, Shohei Ohue, Shiro Ohnishi, Takanori Kunieda, Takeharu Neurooncol Adv Supplement Abstracts Analysis of exosomes derived from plasma or cerebrospinal fluid (CSF) has emerged as a promising biomarker platform for therapeutic monitoring in glioblastoma patients. However, the contents of the various subpopulations of exosomes in these clinical specimens remain poorly defined. Here we characterize the relative abundance of miRNA species in exosomes derived from the plasma and CSF of glioblastoma patients. To this end, we first employed miRNA arrays to measure the expression of exosomal miRNAs in the plasma from glioblastoma patients (n = 24) and healthy volunteers (n = 7) as control. In addition, we performed global miRNA profiling of exosomal miRNAs in the CSF from glioblastoma patients (n = 5) and non-tumoral patients (n = 3; hydrocephalus patients) as control. In plasma derived exosomes, 80 miRNAs were altered by >2-fold in glioblastoma patients compared to controls. In CSF, 92 miRNAs were altered by >2-fold in glioblastoma patients compared to controls. Combined analysis of plasma and CSF revealed a similar fold difference in eight miRNAs. Next, we measured these eight miRNAs expression in in the plasma from pre- and post-operative glioblastoma patients (n = 9). Among these eight miRNAs, we identified only one miRNA (miR-34b-3p) that was upregulated in exosomes from pre-operative glioblastoma patients. Our results suggest that miR-34b-3p might have a potential as a novel diagnostic marker or a therapeutic tool for glioblastoma patients. Oxford University Press 2021-12-06 /pmc/articles/PMC8648223/ http://dx.doi.org/10.1093/noajnl/vdab159.111 Text en © The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement Abstracts
Yamashita, Daisuke
Suehiro, Satoshi
Ohtsuka, Yoshihiro
Ozaki, Saya
Nishikawa, Masahiro
Inoue, Akihiro
Kohno, Shohei
Ohue, Shiro
Ohnishi, Takanori
Kunieda, Takeharu
COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients
title COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients
title_full COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients
title_fullStr COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients
title_full_unstemmed COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients
title_short COT-3 Exosomal microRNA expression signature in blood and cerebrospinal fluid of glioblastoma patients
title_sort cot-3 exosomal microrna expression signature in blood and cerebrospinal fluid of glioblastoma patients
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648223/
http://dx.doi.org/10.1093/noajnl/vdab159.111
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