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Initial testing of the investigational NEDD8-activating enzyme inhibitor MLN4924 by the pediatric preclinical testing program

  • Malcolm A. Smith
  • , John M. Maris
  • , Richard Gorlick
  • , E. Anders Kolb
  • , Richard Lock
  • , Hernan Carol
  • , Stephen T. Keir
  • , C. Patrick Reynolds
  • , Min H. Kang
  • , Christopher L. Morton
  • , Jianrong Wu
  • , Peter G. Smith
  • , Jie Yu
  • , Peter J. Houghton

Producción científica: Articlerevisión exhaustiva

31 Citas (Scopus)

Resumen

Background: MLN4924 is an investigational first-in-class small molecule inhibitor of NEDD8-activating enzyme (NAE). NAE is an essential component of the NEDD8 conjugation pathway, controlling the activity of a subset of ubiquitin-proteasome system (UPS) E3 ligases, multiprotein complexes that transfer ubiquitin molecules to substrate proteins. Procedures: MLN4924 was tested against the PPTP in vitro panel using 96-hour exposure time at concentrations ranging from 1.0nM to 10μM. It was tested in vivo at a dose of 100mg/kg [66mg/kg for the acute lymphoblastic leukemia (ALL) xenografts] administered orally twice daily×5 days. Treatment duration was 3 weeks. Results: The median relative IC 50 for MLN4924 against the PPTP cell lines was 143nM, (range: 15-678nM) with that for the Ewing panel being significantly lower (31nM). MLN4924 induced significant differences in EFS distribution compared to control in 20 of 34 (59%) evaluable solid tumor xenografts. MLN4924 induced intermediate activity (EFS T/C values >2) in 9 of the 33 evaluable xenografts (27%), including 4 of 4 glioblastoma xenografts, 2 of 3 Wilm's tumor xenografts, 2 of 5 rhabdomyosarcoma xenografts, and 1 of 4 neuroblastoma xenografts. For the ALL panel, 5 of 8 evaluable xenografts showed intermediate activity for the EFS T/C measure. MLN4924 did not induce objective responses in the PPTP solid tumor or ALL panels. Conclusions: MLN4924 showed potent activity in vitro and in vivo showed tumor growth inhibitory activity against a subset of the PPTP solid tumor and ALL xenografts.

Idioma originalEnglish
Páginas (desde-hasta)246-253
Número de páginas8
PublicaciónPediatric Blood and Cancer
Volumen59
N.º2
DOI
EstadoPublished - ago 2012

Financiación

FinanciadoresNúmero del financiador
National Childhood Cancer Registry – National Cancer InstituteP50CA108786

    ASJC Scopus subject areas

    • Pediatrics, Perinatology, and Child Health
    • Hematology
    • Oncology

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