The cell cycle regulator 14-3-3σ opposes and reverses cancer metabolic reprogramming

Nat Commun. 2015 Jul 16:6:7530. doi: 10.1038/ncomms8530.

Abstract

Extensive reprogramming of cellular energy metabolism is a hallmark of cancer. Despite its importance, the molecular mechanism controlling this tumour metabolic shift remains not fully understood. Here we show that 14-3-3σ regulates cancer metabolic reprogramming and protects cells from tumorigenic transformation. 14-3-3σ opposes tumour-promoting metabolic programmes by enhancing c-Myc poly-ubiquitination and subsequent degradation. 14-3-3σ demonstrates the suppressive impact on cancer glycolysis, glutaminolysis, mitochondrial biogenesis and other major metabolic processes of tumours. Importantly, 14-3-3σ expression levels predict overall and recurrence-free survival rates, tumour glucose uptake and metabolic gene expression in breast cancer patients. Thus, these results highlight that 14-3-3σ is an important regulator of tumour metabolism, and loss of 14-3-3σ expression is critical for cancer metabolic reprogramming. We anticipate that pharmacologically elevating the function of 14-3-3σ in tumours could be a promising direction for targeted anticancer metabolism therapy development in future.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 14-3-3 Proteins / genetics*
  • 14-3-3 Proteins / metabolism
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / metabolism
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / metabolism
  • Cell Line, Tumor
  • Disease-Free Survival
  • Energy Metabolism / genetics*
  • Exoribonucleases / genetics*
  • Exoribonucleases / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Gene Knockout Techniques
  • Glutamine / metabolism
  • Glycolysis / genetics
  • HCT116 Cells
  • Humans
  • Middle Aged
  • Organelle Biogenesis
  • Prognosis
  • Proteolysis
  • Proto-Oncogene Proteins c-myc / metabolism*
  • Ubiquitination / genetics
  • Young Adult

Substances

  • 14-3-3 Proteins
  • Biomarkers, Tumor
  • MYC protein, human
  • Proto-Oncogene Proteins c-myc
  • Glutamine
  • Exoribonucleases
  • SFN protein, human