Involvement of general control nonderepressible kinase 2 in cancer cell apoptosis by posttranslational mechanisms

Mol Biol Cell. 2015 Mar 15;26(6):1044-57. doi: 10.1091/mbc.E14-10-1438. Epub 2015 Jan 14.

Abstract

General control nonderepressible kinase 2 (GCN2) is a promising target for cancer therapy. However, the role of GCN2 in cancer cell survival or death is elusive; further, small molecules targeting GCN2 signaling are not available. By using a GCN2 level-based drug screening assay, we found that GCN2 protein level critically determined the sensitivity of the cancer cells toward Na(+),K(+)-ATPase ligand-induced apoptosis both in vitro and in vivo, and this effect was largely dependent on C/EBP homologous protein (CHOP) induction. Further analysis revealed that GCN2 is a short-lived protein. In A549 lung carcinoma cells, cellular β-arrestin1/2 associated with GCN2 and maintained the GCN2 protein level at a low level by recruiting the E3 ligase NEDD4L and facilitating consequent proteasomal degradation. However, Na(+),K(+)-ATPase ligand treatment triggered the phosphorylation of GCN2 at threonine 899, which increased the GCN2 protein level by disrupting the formation of GCN2-β-arrestin-NEDD4L ternary complex. The enhanced GCN2 level, in turn, aggravated Na(+),K(+)-ATPase ligand-induced cancer cell apoptosis. Our findings reveal that GCN2 can exert its proapoptotic function in cancer cell death by posttranslational mechanisms. Moreover, Na(+),K(+)-ATPase ligands emerge as the first identified small-molecule drugs that can trigger cancer cell death by modulating GCN2 signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Arrestins / metabolism
  • Endosomal Sorting Complexes Required for Transport / metabolism
  • Gene Expression
  • HCT116 Cells
  • HT29 Cells
  • Humans
  • Nedd4 Ubiquitin Protein Ligases
  • Phosphorylation
  • Protein Serine-Threonine Kinases / physiology*
  • Proteolysis
  • Transcription Factor CHOP / metabolism
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination*
  • beta-Arrestins

Substances

  • Arrestins
  • DDIT3 protein, human
  • Endosomal Sorting Complexes Required for Transport
  • beta-Arrestins
  • Transcription Factor CHOP
  • Nedd4 Ubiquitin Protein Ligases
  • Nedd4L protein, human
  • Ubiquitin-Protein Ligases
  • EIF2AK4 protein, human
  • Protein Serine-Threonine Kinases