Molecular sequelae of proteasome inhibition in human multiple myeloma cells
Massachusetts Eye and Ear Infirmary · Beth Israel Deaconess Medical Center · +2 more institutions
Abstract
The proteasome inhibitor PS-341 inhibits IkappaB degradation, prevents NF-kappaB activation, and induces apoptosis in several types of cancer cells, including chemoresistant multiple myeloma (MM) cells. PS-341 has marked clinical activity even in the setting of relapsed refractory MM. However, PS-341-induced apoptotic cascade(s) are not yet fully defined. By using gene expression profiling, we characterized the molecular sequelae of PS-341 treatment in MM cells and further focused on molecular pathways responsible for the anticancer actions of this promising agent. The transcriptional profile of PS-341-treated cells involved down-regulation of growth/survival signaling pathways, and up-regulation of molecules…
Citation impact
- FWCI
- 18.75
- Percentile
- 100%
- References
- 62
Authors
14- NMNicholas Mitsiades
Massachusetts Eye and Ear Infirmary, Beth Israel Deaconess Medical Center, Harvard University, Dana-Farber Cancer Institute
- CMConstantine Mitsiades
Massachusetts Eye and Ear Infirmary, Beth Israel Deaconess Medical Center, Harvard University, Dana-Farber Cancer Institute
- VPVassiliki Poulaki
Massachusetts Eye and Ear Infirmary, Beth Israel Deaconess Medical Center, Harvard University, Dana-Farber Cancer Institute
- DCDharminder Chauhan
Massachusetts Eye and Ear Infirmary, Beth Israel Deaconess Medical Center, Harvard University, Dana-Farber Cancer Institute
- GFGalinos Fanourakis
Massachusetts Eye and Ear Infirmary, Beth Israel Deaconess Medical Center, Harvard University, Dana-Farber Cancer Institute
Topics & keywords
- Proteasome
- Bortezomib
- Apoptosis
- Protein kinase B
- Cell biology
- Proteasome inhibitor
- Biology
- Signal transduction
- Good health and well-being