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Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks
Molecular classification has improved the knowledge of medulloblastoma (MB), the most common malignant brain tumour in children, however current treatments cause severe side effects in patients. Cancer stem cells (CSCs) have been described in MB and represent a sub population characterised by self-r...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121264/ https://www.ncbi.nlm.nih.gov/pubmed/30096798 http://dx.doi.org/10.3390/ijms19082326 |
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author | Po, Agnese Abballe, Luana Sabato, Claudia Gianno, Francesca Chiacchiarini, Martina Catanzaro, Giuseppina De Smaele, Enrico Giangaspero, Felice Ferretti, Elisabetta Miele, Evelina Besharat, Zein Mersini |
author_facet | Po, Agnese Abballe, Luana Sabato, Claudia Gianno, Francesca Chiacchiarini, Martina Catanzaro, Giuseppina De Smaele, Enrico Giangaspero, Felice Ferretti, Elisabetta Miele, Evelina Besharat, Zein Mersini |
author_sort | Po, Agnese |
collection | PubMed |
description | Molecular classification has improved the knowledge of medulloblastoma (MB), the most common malignant brain tumour in children, however current treatments cause severe side effects in patients. Cancer stem cells (CSCs) have been described in MB and represent a sub population characterised by self-renewal and the ability to generate tumour cells, thus representing the reservoir of the tumour. To investigate molecular pathways that characterise this sub population, we isolated CSCs from Sonic Hedgehog Medulloblastoma (SHH MB) arisen in Patched 1 (Ptch1) heterozygous mice, and performed miRNA- and mRNA-sequencing. Comparison of the miRNA-sequencing of SHH MB CSCs with that obtained from cerebellar Neural Stem Cells (NSCs), allowed us to obtain a SHH MB CSC miRNA differential signature. Pathway enrichment analysis in SHH MB CSCs mirnome and transcriptome was performed and revealed a series of enriched pathways. We focused on the putative targets of the SHH MB CSC miRNAs that were involved in the enriched pathways of interest, namely pathways in cancer, PI3k-Akt pathway and protein processing in endoplasmic reticulum pathway. In silico analysis was performed in SHH MB patients and identified several genes, whose expression was associated with worse overall survival of SHH MB patients. This study provides novel candidates whose functional role should be further investigated in SHH MB. |
format | Online Article Text |
id | pubmed-6121264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61212642018-09-07 Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks Po, Agnese Abballe, Luana Sabato, Claudia Gianno, Francesca Chiacchiarini, Martina Catanzaro, Giuseppina De Smaele, Enrico Giangaspero, Felice Ferretti, Elisabetta Miele, Evelina Besharat, Zein Mersini Int J Mol Sci Article Molecular classification has improved the knowledge of medulloblastoma (MB), the most common malignant brain tumour in children, however current treatments cause severe side effects in patients. Cancer stem cells (CSCs) have been described in MB and represent a sub population characterised by self-renewal and the ability to generate tumour cells, thus representing the reservoir of the tumour. To investigate molecular pathways that characterise this sub population, we isolated CSCs from Sonic Hedgehog Medulloblastoma (SHH MB) arisen in Patched 1 (Ptch1) heterozygous mice, and performed miRNA- and mRNA-sequencing. Comparison of the miRNA-sequencing of SHH MB CSCs with that obtained from cerebellar Neural Stem Cells (NSCs), allowed us to obtain a SHH MB CSC miRNA differential signature. Pathway enrichment analysis in SHH MB CSCs mirnome and transcriptome was performed and revealed a series of enriched pathways. We focused on the putative targets of the SHH MB CSC miRNAs that were involved in the enriched pathways of interest, namely pathways in cancer, PI3k-Akt pathway and protein processing in endoplasmic reticulum pathway. In silico analysis was performed in SHH MB patients and identified several genes, whose expression was associated with worse overall survival of SHH MB patients. This study provides novel candidates whose functional role should be further investigated in SHH MB. MDPI 2018-08-08 /pmc/articles/PMC6121264/ /pubmed/30096798 http://dx.doi.org/10.3390/ijms19082326 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Po, Agnese Abballe, Luana Sabato, Claudia Gianno, Francesca Chiacchiarini, Martina Catanzaro, Giuseppina De Smaele, Enrico Giangaspero, Felice Ferretti, Elisabetta Miele, Evelina Besharat, Zein Mersini Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks |
title | Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks |
title_full | Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks |
title_fullStr | Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks |
title_full_unstemmed | Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks |
title_short | Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks |
title_sort | sonic hedgehog medulloblastoma cancer stem cells mirnome and transcriptome highlight novel functional networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121264/ https://www.ncbi.nlm.nih.gov/pubmed/30096798 http://dx.doi.org/10.3390/ijms19082326 |
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