The eEF2 kinase confers resistance to nutrient deprivation by blocking translation elongation

Cell. 2013 May 23;153(5):1064-79. doi: 10.1016/j.cell.2013.04.055.

Abstract

Metabolic adaptation is essential for cell survival during nutrient deprivation. We report that eukaryotic elongation factor 2 kinase (eEF2K), which is activated by AMP-kinase (AMPK), confers cell survival under acute nutrient depletion by blocking translation elongation. Tumor cells exploit this pathway to adapt to nutrient deprivation by reactivating the AMPK-eEF2K axis. Adaptation of transformed cells to nutrient withdrawal is severely compromised in cells lacking eEF2K. Moreover, eEF2K knockdown restored sensitivity to acute nutrient deprivation in highly resistant human tumor cell lines. In vivo, overexpression of eEF2K rendered murine tumors remarkably resistant to caloric restriction. Expression of eEF2K strongly correlated with overall survival in human medulloblastoma and glioblastoma multiforme. Finally, C. elegans strains deficient in efk-1, the eEF2K ortholog, were severely compromised in their response to nutrient depletion. Our data highlight a conserved role for eEF2K in protecting cells from nutrient deprivation and in conferring tumor cell adaptation to metabolic stress. PAPERCLIP:

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Brain Neoplasms / physiopathology
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Cell Survival
  • Cell Transformation, Neoplastic
  • Elongation Factor 2 Kinase / genetics
  • Elongation Factor 2 Kinase / metabolism*
  • Food Deprivation
  • Glioblastoma / physiopathology
  • HeLa Cells
  • Humans
  • Mice
  • Mice, Nude
  • NIH 3T3 Cells
  • Neoplasm Transplantation
  • Neoplasms / physiopathology*
  • Peptide Chain Elongation, Translational*
  • Peptide Elongation Factor 2 / metabolism
  • Signal Transduction*
  • Transplantation, Heterologous

Substances

  • Peptide Elongation Factor 2
  • Elongation Factor 2 Kinase
  • AMP-Activated Protein Kinases