Cargando…
Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells
High-grade gliomas (HGGs) are very aggressive brain tumors with a cancer stem cell component. Cells, including cancer stem cells, release vesicles called exosomes which contain small non-coding RNAs such as microRNAs (miRNAs). These are thought to play an important role in cell-cell communication. H...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685739/ https://www.ncbi.nlm.nih.gov/pubmed/29163818 http://dx.doi.org/10.18632/oncotarget.21621 |
_version_ | 1783278677572714496 |
---|---|
author | Tűzesi, Ágota Kling, Teresia Wenger, Anna Lunavat, Taral R. Jang, Su Chul Rydenhag, Bertil Lötvall, Jan Pollard, Steven M. Danielsson, Anna Carén, Helena |
author_facet | Tűzesi, Ágota Kling, Teresia Wenger, Anna Lunavat, Taral R. Jang, Su Chul Rydenhag, Bertil Lötvall, Jan Pollard, Steven M. Danielsson, Anna Carén, Helena |
author_sort | Tűzesi, Ágota |
collection | PubMed |
description | High-grade gliomas (HGGs) are very aggressive brain tumors with a cancer stem cell component. Cells, including cancer stem cells, release vesicles called exosomes which contain small non-coding RNAs such as microRNAs (miRNAs). These are thought to play an important role in cell-cell communication. However, we have limited knowledge of the types of exosomal miRNAs released by pediatric HGG stem cells; a prerequisite for exploring their potential roles in HGG biology. Here we isolated exosomes released by pediatric glioma stem cells (GSCs) and compared their repertoire of miRNAs to genetically normal neural stem cells (NSCs) exosomes, as well as their respective cellular miRNA content. Whereas cellular miRNAs are similar, we find that the exosomal miRNA profiles differ between normal and tumor cells, and identify several differentially expressed miRNAs. Of particular interest is miR-1290 and miR-1246, which have previously been linked to ‘stemness’ and invasion in other cancers. We demonstrate that GSC-secreted exosomes influence the gene expression of receiving NSCs, particularly targeting genes with a role in cell fate and tumorigenesis. Thus, our study shows that GSCs and NSCs have similar cellular miRNA profiles, yet differ significantly in the repertoire of exosomal miRNAs and these could influence malignant features of HGG. |
format | Online Article Text |
id | pubmed-5685739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56857392017-11-21 Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells Tűzesi, Ágota Kling, Teresia Wenger, Anna Lunavat, Taral R. Jang, Su Chul Rydenhag, Bertil Lötvall, Jan Pollard, Steven M. Danielsson, Anna Carén, Helena Oncotarget Research Paper High-grade gliomas (HGGs) are very aggressive brain tumors with a cancer stem cell component. Cells, including cancer stem cells, release vesicles called exosomes which contain small non-coding RNAs such as microRNAs (miRNAs). These are thought to play an important role in cell-cell communication. However, we have limited knowledge of the types of exosomal miRNAs released by pediatric HGG stem cells; a prerequisite for exploring their potential roles in HGG biology. Here we isolated exosomes released by pediatric glioma stem cells (GSCs) and compared their repertoire of miRNAs to genetically normal neural stem cells (NSCs) exosomes, as well as their respective cellular miRNA content. Whereas cellular miRNAs are similar, we find that the exosomal miRNA profiles differ between normal and tumor cells, and identify several differentially expressed miRNAs. Of particular interest is miR-1290 and miR-1246, which have previously been linked to ‘stemness’ and invasion in other cancers. We demonstrate that GSC-secreted exosomes influence the gene expression of receiving NSCs, particularly targeting genes with a role in cell fate and tumorigenesis. Thus, our study shows that GSCs and NSCs have similar cellular miRNA profiles, yet differ significantly in the repertoire of exosomal miRNAs and these could influence malignant features of HGG. Impact Journals LLC 2017-10-06 /pmc/articles/PMC5685739/ /pubmed/29163818 http://dx.doi.org/10.18632/oncotarget.21621 Text en Copyright: © 2017 Tűzesi et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Tűzesi, Ágota Kling, Teresia Wenger, Anna Lunavat, Taral R. Jang, Su Chul Rydenhag, Bertil Lötvall, Jan Pollard, Steven M. Danielsson, Anna Carén, Helena Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells |
title | Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells |
title_full | Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells |
title_fullStr | Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells |
title_full_unstemmed | Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells |
title_short | Pediatric brain tumor cells release exosomes with a miRNA repertoire that differs from exosomes secreted by normal cells |
title_sort | pediatric brain tumor cells release exosomes with a mirna repertoire that differs from exosomes secreted by normal cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685739/ https://www.ncbi.nlm.nih.gov/pubmed/29163818 http://dx.doi.org/10.18632/oncotarget.21621 |
work_keys_str_mv | AT tuzesiagota pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT klingteresia pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT wengeranna pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT lunavattaralr pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT jangsuchul pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT rydenhagbertil pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT lotvalljan pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT pollardstevenm pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT danielssonanna pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells AT carenhelena pediatricbraintumorcellsreleaseexosomeswithamirnarepertoirethatdiffersfromexosomessecretedbynormalcells |