Multiple myeloma cells depend on the DDI2/NRF1-mediated proteasome stress response for survival
Multiple myeloma (MM) cells suffer from baseline proteotoxicity as the result of an imbalance
between the load of misfolded proteins awaiting proteolysis and the capacity of the ubiquitin …
between the load of misfolded proteins awaiting proteolysis and the capacity of the ubiquitin …
The aspartyl protease DDI2 drives adaptation to proteasome inhibition in multiple myeloma
M Op, ST Ribeiro, C Chavarria, A De Gassart… - Cell death & …, 2022 - nature.com
Proteasome inhibitors, such as bortezomib, are first-line therapy against multiple myeloma
(MM). Unfortunately, patients frequently become refractory to this treatment. The transcription …
(MM). Unfortunately, patients frequently become refractory to this treatment. The transcription …
Renal medullary carcinomas depend upon SMARCB1 loss and are sensitive to proteasome inhibition
Renal medullary carcinoma (RMC) is a rare and deadly kidney cancer in patients of African
descent with sickle cell trait. We have developed faithful patient-derived RMC models and …
descent with sickle cell trait. We have developed faithful patient-derived RMC models and …
Marizomib irreversibly inhibits proteasome to overcome compensatory hyperactivation in multiple myeloma and solid tumour patients
N Levin, A Spencer, SJ Harrison… - British journal of …, 2016 - Wiley Online Library
Proteasome inhibitors (PI s) are highly active in multiple myeloma (MM) but resistance is
commonly observed. All clinical stage PI s effectively inhibit chymotrypsin‐like (CT‐L) …
commonly observed. All clinical stage PI s effectively inhibit chymotrypsin‐like (CT‐L) …
NF-κB dysregulation in multiple myeloma
GM Matthews, R de Matos Simoes, E Dhimolea… - Seminars in cancer …, 2016 - Elsevier
The nuclear factor-κB (NF-κB) transcription factor family plays critical roles in the
pathophysiology of hematologic neoplasias, including multiple myeloma. The current review …
pathophysiology of hematologic neoplasias, including multiple myeloma. The current review …
Targeting the ubiquitin-proteasome system in atherosclerosis: status quo, challenges, and perspectives
N Wilck, A Ludwig - Antioxidants & redox signaling, 2014 - liebertpub.com
Significance: Atherosclerosis is a vascular disease of worldwide significance with fatal
complications such as myocardial infarction, stroke, and peripheral artery disease …
complications such as myocardial infarction, stroke, and peripheral artery disease …
An inhibitor of proteasome β2 sites sensitizes myeloma cells to immunoproteasome inhibitors
S Downey-Kopyscinski, EW Daily, M Gautier… - Blood …, 2018 - ashpublications.org
Proteasome inhibitors bortezomib, carfilzomib and ixazomib (approved by the US Food and
Drug Administration [FDA]) induce remissions in patients with multiple myeloma (MM), but …
Drug Administration [FDA]) induce remissions in patients with multiple myeloma (MM), but …
Molecular mechanisms of bortezomib action: novel evidence for the miRNA–mRNA interaction involvement
K Łuczkowska, D Rogińska, Z Ulańczyk… - International Journal of …, 2020 - mdpi.com
Bortezomib is an anti-tumor agent, which inhibits 26S proteasome degrading ubiquitinated
proteins. While apoptotic transcription-associated activation in response to bortezomib has …
proteins. While apoptotic transcription-associated activation in response to bortezomib has …
Targeting the biophysical properties of the myeloma initiating cell niches: a pharmaceutical synergism analysis using multi-scale agent-based modeling
Multiple myeloma, the second most common hematological cancer, is currently incurable
due to refractory disease relapse and development of multiple drug resistance. We and …
due to refractory disease relapse and development of multiple drug resistance. We and …
Functional relevance of in vivo half antibody exchange of an IgG4 therapeutic antibody-drug conjugate
P Herbener, K Schönfeld, M König, M Germer… - PloS one, 2018 - journals.plos.org
An increasing number of monoclonal antibodies and derivatives such as antibody-drug
conjugates (ADC) are of the IgG1 and IgG4 isotype with distinct structural and functional …
conjugates (ADC) are of the IgG1 and IgG4 isotype with distinct structural and functional …