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

被引:16
|
作者
El-Mesery, Mohamed [1 ,2 ]
Rosenthal, Tina [2 ]
Rauert-Wunderlich, Hilka [3 ,4 ]
Schreder, Martin [5 ]
Stuehmer, Thorsten [5 ]
Leich, Ellen [3 ]
Schlosser, Andreas [6 ]
Ehrenschwender, Martin [7 ]
Wajant, Harald [2 ]
Siegmund, Daniela [2 ]
机构
[1] Mansoura Univ, Fac Pharm, Dept Biochem, Mansoura, Egypt
[2] Univ Hosp Wurzburg, Dept Internal Med 2, Div Mol Internal Med, Auvera Haus Grombuhlstr 12, D-97080 Wurzburg, Germany
[3] Univ Wurzburg, Inst Pathol, Josef Schneider Str 2, D-97080 Wurzburg, Germany
[4] Univ Hosp Wurzburg, Comprehens Canc Ctr Mainfranken, D-97080 Wurzburg, Germany
[5] Univ Hosp Wurzburg, Comprehens Canc Ctr Mainfranken, Lehrstuhl Translat Onkol, Versbacher Str 5, D-97078 Wurzburg, Germany
[6] Univ Wurzburg, Rudolf Virchow Ctr Expt Biomed, Josef Schneider Str 2, D-97080 Wurzburg, Germany
[7] Univ Hosp Regensburg, Inst Clin Microbiol & Hyg, Franz Josef Str Allee 11, D-93053 Regensburg, Germany
关键词
NF-KAPPA-B; NECROSIS-FACTOR-ALPHA; PEVONEDISTAT TAK-924/MLN4924; PHASE-I; ACTIVATION; CYTOKINES; CANCER; PROLIFERATION; PROTEIN; C-IAP2;
D O I
10.1038/s41419-019-1860-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The NEDD8-activating enzyme (NAE) inhibitor MLN4924 inhibits cullin-RING ubiquitin ligase complexes including the SKP1-cullin-F-box E3 ligase beta TrCP. MLN4924 therefore inhibits also the beta TrCP-dependent activation of the classical and the alternative NF kappa B 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 NF kappa B 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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页数:15
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