Autophagic and Apoptotic Pathways as Targets for Chemotherapy in Glioblastoma

Int J Mol Sci. 2018 Nov 27;19(12):3773. doi: 10.3390/ijms19123773.

Abstract

Glioblastoma multiforme is the most malignant and aggressive type of brain tumor, with a mean life expectancy of less than 15 months. This is due in part to the high resistance to apoptosis and moderate resistant to autophagic cell death in glioblastoma cells, and to the poor therapeutic response to conventional therapies. Autophagic cell death represents an alternative mechanism to overcome the resistance of glioblastoma to pro-apoptosis-related therapies. Nevertheless, apoptosis induction plays a major conceptual role in several experimental studies to develop novel therapies against brain tumors. In this review, we outline the different components of the apoptotic and autophagic pathways and explore the mechanisms of resistance to these cell death pathways in glioblastoma cells. Finally, we discuss drugs with clinical and preclinical use that interfere with the mechanisms of survival, proliferation, angiogenesis, migration, invasion, and cell death of malignant cells, favoring the induction of apoptosis and autophagy, or the inhibition of the latter leading to cell death, as well as their therapeutic potential in glioma, and examine new perspectives in this promising research field.

Keywords: apoptosis; autophagia; chemotherapy; glioblastoma; signaling pathways; therapeutic targets.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects*
  • Autophagy / drug effects*
  • Biomarkers
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism
  • Clinical Trials as Topic
  • Drug Discovery
  • Gene Expression Regulation, Neoplastic
  • Glioblastoma / drug therapy
  • Glioblastoma / genetics
  • Glioblastoma / metabolism*
  • Glioblastoma / pathology
  • Glioma / drug therapy
  • Glioma / genetics
  • Glioma / metabolism
  • Glioma / pathology
  • Humans
  • Molecular Targeted Therapy
  • Signal Transduction / drug effects*
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Biomarkers