Metabolic alterations in multiple myeloma: from oncogenesis to proteasome inhibitor resistance

Philip Weir, David Donaldson, Mary Frances McMullin, Lisa Crawford*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

1 Citation (Scopus)
156 Downloads (Pure)

Abstract

Despite significant improvements in treatment strategies over the past couple of decades, multiple myeloma (MM) remains an incurable disease due to the development of drug resistance. Metabolic reprogramming is a key feature of cancer cells, including MM, and acts to fuel increased proliferation, create a permissive tumour microenvironment, and promote drug resistance. This review presents an overview of the key metabolic adaptations that occur in MM pathogenesis and in the development of resistance to proteasome inhibitors, the backbone of current MM therapy, and considers the potential for therapeutic targeting of key metabolic pathways to improve outcomes.
Original languageEnglish
Article number1682
JournalCancers
Volume15
Issue number6
DOIs
Publication statusPublished - 09 Mar 2023

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