The NEDD8-activating enzyme inhibitor MLN4924 sensitizes a TNFR1+ subgroup of multiple myeloma cells for TNF-induced cell death

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作者
Mohamed El-Mesery
Tina Rosenthal
Hilka Rauert-Wunderlich
Martin Schreder
Thorsten Stühmer
Ellen Leich
Andreas Schlosser
Martin Ehrenschwender
Harald Wajant
Daniela Siegmund
机构
[1] Mansoura University,Department of Biochemistry, Faculty of Pharmacy
[2] University Hospital Würzburg,Division of Molecular Internal Medicine, Department of Internal Medicine II
[3] University of Würzburg,Institute of Pathology
[4] University Hospital Würzburg,Comprehensive Cancer Center Mainfranken
[5] University Hospital Würzburg,Lehrstuhl für Translationale Onkologie, Comprehensive Cancer Center Mainfranken
[6] University of Würzburg,Rudolf Virchow Center for Experimental Biomedicine
[7] University Hospital Regensburg,Institute of Clinical Microbiology and Hygiene
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The NEDD8-activating enzyme (NAE) inhibitor MLN4924 inhibits cullin-RING ubiquitin ligase complexes including the SKP1-cullin-F-box E3 ligase βTrCP. MLN4924 therefore inhibits also the βTrCP-dependent activation of the classical and the alternative NFĸB pathway. In this work, we found that a subgroup of multiple myeloma cell lines (e.g., RPMI-8226, MM.1S, KMS-12BM) and about half of the primary myeloma samples tested are sensitized to TNF-induced cell death by MLN4924. This correlated with MLN4924-mediated inhibition of TNF-induced activation of the classical NFκB pathway and reduced the efficacy of TNF-induced TNFR1 signaling complex formation. Interestingly, binding studies revealed a straightforward correlation between cell surface TNFR1 expression in multiple myeloma cell lines and their sensitivity for MLN4924/TNF-induced cell death. The cell surface expression levels of TNFR1 in the investigated MM cell lines largely correlated with TNFR1 mRNA expression. This suggests that the variable levels of cell surface expression of TNFR1 in myeloma cell lines are decisive for TNF/MLN4924 sensitivity. Indeed, introduction of TNFR1 into TNFR1-negative TNF/MLN4924-resistant KMS-11BM cells, was sufficient to sensitize this cell line for TNF/MLN4924-induced cell death. Thus, MLN4924 might be especially effective in myeloma patients with TNFR1+ myeloma cells and a TNFhigh tumor microenvironment.
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