Sonic Hedgehog Medulloblastoma Cancer Stem Cells Mirnome and Transcriptome Highlight Novel Functional Networks

Int J Mol Sci. 2018 Aug 8;19(8):2326. doi: 10.3390/ijms19082326.

Abstract

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.

Keywords: RNA-sequencing; Sonic Hedgehog pathway; cancer stem cells; medulloblastoma; microRNAs.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic / genetics
  • Hedgehog Proteins / genetics*
  • Humans
  • Medulloblastoma / genetics*
  • Medulloblastoma / pathology
  • Mice
  • MicroRNAs / genetics*
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Neural Stem Cells / metabolism
  • Neural Stem Cells / pathology
  • Patched-1 Receptor / genetics
  • Phosphatidylinositol 3-Kinases
  • Signal Transduction / genetics
  • Transcriptome / genetics*

Substances

  • Hedgehog Proteins
  • MicroRNAs
  • Patched-1 Receptor
  • Ptch1 protein, mouse
  • Phosphatidylinositol 3-Kinases