Proteasome inhibitors induce a terminal unfolded protein response in multiple myeloma cells
University of Miami · Sylvester Comprehensive Cancer Center
Abstract
Multiple myeloma (MM) is an incurable plasma cell malignancy. The 26S proteasome inhibitor, bortezomib, selectively induces apoptosis in MM cells; however, the nature of its selectivity remains unknown. Here we demonstrate that 5 different MM cell lines display similar patterns of sensitivity to 3 proteasome inhibitors (PIs) but respond differently to specific NF-kappaB inhibition. We further show that PIs initiate the unfolded protein response (UPR), a signaling pathway activated by the accumulation of misfolded proteins within the endoplasmic reticulum (ER). Consistent with reports that prosurvival/physiologic UPR components are required for B-cell differentiation into antibody-secreting cells, we found that…
Citation impact
- FWCI
- 15.10
- Percentile
- 100%
- References
- 106
Authors
6- EAEsther A. ObengCorresponding
University of Miami, Sylvester Comprehensive Cancer Center
- LCLouise Carlson
University of Miami, Sylvester Comprehensive Cancer Center
- DGDelia Gutman
University of Miami, Sylvester Comprehensive Cancer Center
- WJWilliam J. Harrington
University of Miami, Sylvester Comprehensive Cancer Center
- KPKelvin P. Lee
University of Miami, Sylvester Comprehensive Cancer Center
Topics & keywords
- Unfolded protein response
- Bortezomib
- ATF4
- Proteasome
- Endoplasmic reticulum
- Proteasome inhibitor
- Cell biology
- Apoptosis
- Good health and well-being