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Treatment-Emergent Mutations in NAE beta Confer Resistance to the NEDD8-Activating Enzyme Inhibitor MLN4924

  作者 Milhollen, MA; Thomas, MP; Narayanan, U; Traore, T; Riceberg, J; Amidon, BS; Bence, NF; Bolen, JB; Brownell, J; Dick, LR; Loke, HK; McDonald, AA; Ma, JY; Manfredi, MG; Sells, TB; Sintchak, MD; Yang, XF; Xu, Q; Koenig, EM; Gavin, JM; Smith, PG  
  选自 期刊  Cancer Cell;  卷期  2012年21-3;  页码  388-401  
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[摘要]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 NAE beta as the primary mechanism of resistance to MLN4924. Biochemical analyses of NAE beta 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 NAE beta mutations.

 
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