RNA binding protein-mediated post-transcriptional gene regulation in medulloblastoma

Mol Cells. 2014 May;37(5):357-64. doi: 10.14348/molcells.2014.0008. Epub 2014 Mar 6.

Abstract

Medulloblastoma, the most common malignant brain tumor in children, is a disease whose mechanisms are now beginning to be uncovered by high-throughput studies of somatic mutations, mRNA expression patterns, and epigenetic profiles of patient tumors. One emerging theme from studies that sequenced the tumor genomes of large cohorts of medulloblastoma patients is frequent mutation of RNA binding proteins. Proteins which bind multiple RNA targets can act as master regulators of gene expression at the post-transcriptional level to co-ordinate cellular processes and alter the phenotype of the cell. Identification of the target genes of RNA binding proteins may highlight essential pathways of medulloblastomagenesis that cannot be detected by study of transcriptomics alone. Furthermore, a subset of RNA binding proteins are attractive drug targets. For example, compounds that are under development as anti-viral targets due to their ability to inhibit RNA helicases could also be tested in novel approaches to medulloblastoma therapy by targeting key RNA binding proteins. In this review, we discuss a number of RNA binding proteins, including Musashi1 (MSI1), DEAD (Asp-Glu-Ala-Asp) box helicase 3 X-linked (DDX3X), DDX31, and cell division cycle and apoptosis regulator 1 (CCAR1), which play potentially critical roles in the growth and/or maintenance of medulloblastoma.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins / physiology
  • Cell Cycle Proteins / physiology
  • Cerebellar Neoplasms / genetics*
  • Cerebellar Neoplasms / metabolism
  • DEAD-box RNA Helicases / physiology*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Medulloblastoma / genetics*
  • Medulloblastoma / metabolism
  • Nerve Tissue Proteins / physiology*
  • Protein Biosynthesis
  • RNA Interference
  • RNA-Binding Proteins / physiology*

Substances

  • Apoptosis Regulatory Proteins
  • CCAR1 protein, human
  • Cell Cycle Proteins
  • MSI1 protein, human
  • Nerve Tissue Proteins
  • RNA-Binding Proteins
  • DDX31 protein, human
  • DDX3X protein, human
  • DEAD-box RNA Helicases