Treatment-emergent mutations in NAEβ confer resistance to the NEDD8-activating enzyme inhibitor MLN4924

Cancer Cell. 2012 Mar 20;21(3):388-401. doi: 10.1016/j.ccr.2012.02.009.

Abstract

MLN4924 is an investigational small-molecule inhibitor of NEDD8-activating enzyme (NAE) in clinical trials for the treatment of cancer. MLN4924 is a mechanism-based inhibitor, with enzyme inhibition occurring through the formation of a tight-binding NEDD8-MLN4924 adduct. In cell and xenograft models of cancer, we identified treatment-emergent heterozygous mutations in the adenosine triphosphate binding pocket and NEDD8-binding cleft of NAEβ as the primary mechanism of resistance to MLN4924. Biochemical analyses of NAEβ mutants revealed slower rates of adduct formation and reduced adduct affinity for the mutant enzymes. A compound with tighter binding properties was able to potently inhibit mutant enzymes in cells. These data provide rationales for patient selection and the development of next-generation NAE inhibitors designed to overcome treatment-emergent NAEβ mutations.

MeSH terms

  • Animals
  • Binding Sites
  • Cell Line, Tumor
  • Clinical Trials as Topic
  • Cyclopentanes / pharmacology*
  • Drug Resistance, Neoplasm / genetics
  • Enzyme Inhibitors / pharmacology*
  • Female
  • Humans
  • Mice
  • Mice, Nude
  • Mutation*
  • Pyrimidines / pharmacology*
  • Rats
  • Rats, Nude
  • Tumor Cells, Cultured
  • Ubiquitin-Activating Enzymes / chemistry
  • Ubiquitin-Activating Enzymes / genetics*
  • Ubiquitin-Activating Enzymes / physiology
  • Xenograft Model Antitumor Assays

Substances

  • Cyclopentanes
  • Enzyme Inhibitors
  • Pyrimidines
  • Ubiquitin-Activating Enzymes
  • pevonedistat