Migration/Invasion of Malignant Gliomas and Implications for Therapeutic Treatment

Int J Mol Sci. 2018 Apr 8;19(4):1115. doi: 10.3390/ijms19041115.

Abstract

Malignant tumors of the central nervous system (CNS) are among cancers with the poorest prognosis, indicated by their association with tumors of high-level morbidity and mortality. Gliomas, the most common primary CNS tumors that arise from neuroglial stem or progenitor cells, have estimated annual incidence of 6.6 per 100,000 individuals in the USA, and 3.5 per 100,000 individuals in Taiwan. Tumor invasion and metastasis are the major contributors to the deaths in cancer patients. Therapeutic goals including cancer stem cells (CSC), phenotypic shifts, EZH2/AXL/TGF-β axis activation, miRNAs and exosomes are relevant to GBM metastasis to develop novel targeted therapeutics for GBM and other brain cancers. Herein, we highlight tumor metastasis in our understanding of gliomas, and illustrate novel exosome therapeutic approaches in glioma, thereby paving the way towards innovative therapies in neuro-oncology.

Keywords: AXL/EZH2; cancer stem cells; epithelial-mesenchymal transition (EMT); exosomes; glioma; invasion/metastasis; microRNA; phenotypic shift.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Movement*
  • Central Nervous System Neoplasms / drug therapy
  • Central Nervous System Neoplasms / metabolism*
  • Central Nervous System Neoplasms / pathology
  • Enhancer of Zeste Homolog 2 Protein / genetics
  • Enhancer of Zeste Homolog 2 Protein / metabolism
  • Exosomes / metabolism
  • Glioma / drug therapy
  • Glioma / metabolism*
  • Glioma / pathology
  • Humans
  • MicroRNAs / genetics
  • Signal Transduction

Substances

  • MicroRNAs
  • Enhancer of Zeste Homolog 2 Protein