Keeping a breast of recent developments in cancer metabolism

Curr Drug Targets. 2010 Sep;11(9):1112-20. doi: 10.2174/138945010792006861.

Abstract

For decades, it has been recognized that cancer cells display a unique metabolism; specifically, cancer cells have been shown to preferentially utilize glycolysis instead of mitochondrial respiration. This phenomenon is commonly known as the "Warburg effect" after Otto Warburg who first made this observation in 1927. The discovery of the Warburg effect has lead to new methods of detection and differentiation of cancerous tissue and normal tissue. More recently, alterations in cancer metabolism have been researched as a possible target for chemotherapeutic intervention in a number of cancers. The push to understand the metabolism of cancer cells has been particularly acute in breast cancer cells, where multiple novel metabolic mechanisms have recently been described and characterized. However, despite this recent progress, the completion of additional studies on the cellular metabolism of breast cancer cells is necessary before drugs that target cancer cell metabolism could be available to disease-afflicted women. Here, we review recent discoveries in breast cancer cell metabolism as well as current logical drug targets that could be used to alter cell metabolism to promote the selective elimination of breast cancer cells.

Publication types

  • Review

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Cell Death
  • Cell Hypoxia
  • Cell Respiration
  • Cell Survival
  • Female
  • Genes, p53
  • Glucose / metabolism
  • Glycolysis
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Mice
  • Mitochondria / metabolism
  • Molecular Targeted Therapy
  • Phosphoric Monoester Hydrolases
  • Signal Transduction

Substances

  • Apoptosis Regulatory Proteins
  • Intracellular Signaling Peptides and Proteins
  • Phosphoric Monoester Hydrolases
  • TIGAR protein, human
  • Glucose