Ontology highlight
ABSTRACT: Background
Multiple myeloma (MM) is essentially an incurable cancer, but treatments with proteasome inhibitors are widely used clinically to extend patient survival. While the mechanisms of proteasome inhibition by Bortezomib are well known, the cellular responses to this proteotoxic stress that leads to sensitivity by MM are not fully elucidated. This study reports on the application of an emerging method to investigate proteostasis by proteomics.Methods
We utilized metabolic labeling with azidohomoalanine (AHA) in a MM cell line in combination with Bortezomib treatment. AHA labeling facilitates the selective isolation and identification of proteins for investigations of protein synthesis or protein degradation.Results
The data collected reveals significant changes
SUBMITTER: Alhourani L
PROVIDER: S-EPMC12737224 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature