Combination therapy targeting cancer metabolism

Med Hypotheses. 2011 Feb;76(2):169-72. doi: 10.1016/j.mehy.2010.09.008. Epub 2010 Oct 13.

Abstract

Cancer cells undergo significant metabolic adaptation. Cellular transformation enhances both glycolysis and mitochondrial respiration efficiency through the induction of HIF-1α and HIF-2α. In this process, energy production and synthesis of macromolecules are maximized with minimal ROS accumulation. Furthermore, a series of antioxidant enzymes are induced to mitigate the damaging effects of ROS. Examination of these metabolic changes provides rationale for a synergistic approach to combination anti-cancer therapy; targeted inhibition of HIF and inhibition of cellular defenses against oxidative stress.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antioxidants / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Gene Expression Regulation*
  • Glucose / metabolism
  • Glycolysis
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Macromolecular Substances
  • Mitochondria / metabolism
  • Models, Biological
  • Neoplasms / metabolism*
  • Oxidative Stress
  • Reactive Oxygen Species*

Substances

  • Antineoplastic Agents
  • Antioxidants
  • Basic Helix-Loop-Helix Transcription Factors
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Macromolecular Substances
  • Reactive Oxygen Species
  • endothelial PAS domain-containing protein 1
  • Glucose