Journal
BLOOD
Volume 138, Issue 10, Pages 871-884Publisher
AMER SOC HEMATOLOGY
DOI: 10.1182/blood.2020009404
Keywords
-
Categories
Funding
- Collaborative Research Center Transregio [SFB/TR 156, SFB/TR 209]
- Deutsche Forschungsgemeinschaft (DFG)
- DFG under Germany's Excellence Strategy [EXC2180]
- Deutsche Krebshilfe
- Ministry of Health of the Czech Republic [NV19-08-00144]
- Grant Agency of the Czech Republic [GA20-25308S]
- Swiss National Science Foundation [310030 179239]
- Swiss National Science Foundation (SNF) [310030_179239] Funding Source: Swiss National Science Foundation (SNF)
Ask authors/readers for more resources
The study demonstrates the broad antitumor effect of dimethyl fumarate (DMF) on both subtypes of DLBCL by inducing ferroptosis, especially in GCB DLBCL. In ABC DLBCL cells, DMF treatment efficiently inhibits the activity of the IKK complex and Janus kinases. Additionally, the combination of BCL-2-specific BH3 mimetic ABT-199 and an inhibitor of ferroptosis suppressor protein 1 synergize with DMF in inducing cell death in DLBCL.
Despite the development of novel targeted drugs, themolecular heterogeneity of diffuse large B-cell lymphoma (DLBCL) still poses a substantial therapeutic challenge. DLBCL can be classified into at least 2 major subtypes (germinal center B cell [GCB]-like and activated B cell [ABC]-like DLBCL), each characterized by specific gene expression profiles and mutation patterns. Here we demonstrate a broad antitumor effect of dimethyl fumarate (DMF) on both DLBCL subtypes, which is mediated by the induction of ferroptosis, a form of cell death driven by the peroxidation of phospholipids. As a result of the high expression of arachidonate 5-lipoxygenase in concert with low glutathione and glutathione peroxidase 4 levels, DMF induces lipid peroxidation and thus ferroptosis, particularly in GCB DLBCL. In ABC DLBCL cells, which are addicted to NF-kappa B and STAT3 survival signaling, DMF treatment efficiently inhibits the activity of the IKK complex and Janus kinases. Interestingly, the BCL-2-specific BH3 mimetic ABT-199 and an inhibitor of ferroptosis suppressor protein 1 synergize with DMF in inducing cell death in DLBCL. Collectively, our findings identify the clinically approved drug DMF as a promising novel therapeutic option in the treatment of both GCB and ABC DLBCLs.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available