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

Authors :
Xiaofeng Yang
Michael Milhollen
Neil Bence
Mark Manfredi
Huay-Keng Loke
Erik Koenig
James E. Brownell
Mike Sintchak
Michael P. Thomas
Usha Narayanan
Qing Xu
James M. Gavin
Jessica Riceberg
Alice McDonald
Joseph B. Bolen
Benjamin S. Amidon
Peter G. Smith
Sells Todd B
Tary Traore
Jingya Ma
Lawrence R. Dick
Source :
Cancer cell. 21(3)
Publication Year :
2011

Abstract

SummaryMLN4924 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.

Details

ISSN :
18783686
Volume :
21
Issue :
3
Database :
OpenAIRE
Journal :
Cancer cell
Accession number :
edsair.doi.dedup.....5e457e9485395bbbb8c7a947afe140b0