TY - JOUR
T1 - Inhibition of NEDD8-activating enzyme
T2 - A novel approach for the treatment of acute myeloid leukemia
AU - Swords, Ronan T.
AU - Kelly, Kevin R.
AU - Smith, Peter G.
AU - Garnsey, James J.
AU - Mahalingam, Devalingam
AU - Medina, Ernest
AU - Oberheu, Kelli
AU - Padmanabhan, Swaminathan
AU - O'Dwyer, Michael
AU - Nawrocki, Steffan T.
AU - Giles, Francis J.
AU - Carew, Jennifer S.
N1 - Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2010/5/6
Y1 - 2010/5/6
N2 - NEDD8 activating enzyme (NAE) has been identified as an essential regulator of the NEDD8 conjugation pathway, which controls the degradation of many proteins with important roles in cell-cycle progression, DNAdamage, and stress responses. Here we report that MLN4924, a novel inhibitor of NAE, has potent activity in acute myeloid leukemia (AML) models. MLN4924 induced cell death in AML cell lines and primary patient specimens independent of Fms-like tyrosine kinase 3 expression and stromal-mediated survival signaling and led to the stabilization of key NAE targets, inhibition of nuclear factor-κB activity, DNAdamage, and reactive oxygen species generation. Disruption of cellular redox status was shown to be a key event in MLN4924-induced apoptosis. Administration of MLN4924 to mice bearing AML xenografts led to stable disease regression and inhibition of NEDDy-lated cullins. Our findings indicate that MLN4924 is a highly promising novel agent that has advanced into clinical trials for the treatment of AML.
AB - NEDD8 activating enzyme (NAE) has been identified as an essential regulator of the NEDD8 conjugation pathway, which controls the degradation of many proteins with important roles in cell-cycle progression, DNAdamage, and stress responses. Here we report that MLN4924, a novel inhibitor of NAE, has potent activity in acute myeloid leukemia (AML) models. MLN4924 induced cell death in AML cell lines and primary patient specimens independent of Fms-like tyrosine kinase 3 expression and stromal-mediated survival signaling and led to the stabilization of key NAE targets, inhibition of nuclear factor-κB activity, DNAdamage, and reactive oxygen species generation. Disruption of cellular redox status was shown to be a key event in MLN4924-induced apoptosis. Administration of MLN4924 to mice bearing AML xenografts led to stable disease regression and inhibition of NEDDy-lated cullins. Our findings indicate that MLN4924 is a highly promising novel agent that has advanced into clinical trials for the treatment of AML.
UR - http://www.scopus.com/inward/record.url?scp=77952558703&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77952558703&partnerID=8YFLogxK
U2 - 10.1182/blood-2009-11-254862
DO - 10.1182/blood-2009-11-254862
M3 - Article
C2 - 20203261
AN - SCOPUS:77952558703
SN - 0006-4971
VL - 115
SP - 3796
EP - 3800
JO - Blood
JF - Blood
IS - 18
ER -