Mitochondrial biogenesis in epithelial cancer cells promotes breast cancer tumor growth and confers autophagy resistance

Cell Cycle. 2012 Nov 15;11(22):4174-80. doi: 10.4161/cc.22376. Epub 2012 Oct 15.

Abstract

Here, we set out to test the novel hypothesis that increased mitochondrial biogenesis in epithelial cancer cells would "fuel" enhanced tumor growth. For this purpose, we generated MDA-MB-231 cells (a triple-negative human breast cancer cell line) overexpressing PGC-1α and MitoNEET, which are established molecules that drive mitochondrial biogenesis and increased mitochondrial oxidative phosphorylation (OXPHOS). Interestingly, both PGC-1α and MitoNEET increased the abundance of OXPHOS protein complexes, conferred autophagy resistance under conditions of starvation and increased tumor growth by up to ~3-fold. However, this increase in tumor growth was independent of neo-angiogenesis, as assessed by immunostaining and quantitation of vessel density using CD31 antibodies. Quantitatively similar increases in tumor growth were also observed by overexpression of PGC-1β and POLRMT in MDA-MB-231 cells, which are also responsible for mediating increased mitochondrial biogenesis. Thus, we propose that increased mitochondrial "power" in epithelial cancer cells oncogenically promotes tumor growth by conferring autophagy resistance. As such, PGC-1α, PGC-1β, mitoNEET and POLRMT should all be considered as tumor promoters or "metabolic oncogenes." Our results are consistent with numerous previous clinical studies showing that metformin (a weak mitochondrial "poison") prevents the onset of nearly all types of human cancers in diabetic patients. Therefore, metformin (a complex I inhibitor) and other mitochondrial inhibitors should be developed as novel anticancer therapies, targeting mitochondrial metabolism in cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy*
  • Breast Neoplasms / blood supply
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Carrier Proteins / metabolism
  • Cell Line, Tumor
  • DNA-Directed RNA Polymerases / metabolism
  • Female
  • Heat-Shock Proteins / metabolism
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Metformin / pharmacology
  • Mice
  • Mice, Nude
  • Mitochondria / metabolism*
  • Mitochondrial Proteins / metabolism
  • Mitochondrial Turnover / drug effects
  • Neovascularization, Pathologic
  • Oxidative Phosphorylation
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA-Binding Proteins
  • Transcription Factors / metabolism
  • Transfection
  • Transplantation, Heterologous

Substances

  • CISD1 protein, human
  • Carrier Proteins
  • Heat-Shock Proteins
  • Hypoglycemic Agents
  • Mitochondrial Proteins
  • PPARGC1A protein, human
  • PPARGC1B protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA-Binding Proteins
  • Transcription Factors
  • Metformin
  • DNA-Directed RNA Polymerases
  • POLRMT protein, human