Cited by 53Multiple Myeloma Research and TreatmentsUbiquitin and proteasome pathwaysDrug Transport and Resistance Mechanisms

Acquisition of a multidrug-resistant phenotype with a proteasome inhibitor in multiple myeloma

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Gutman, D, Morales, A A, Boise, L H·2009·Leukemia

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Registry

Crossref · 10.1038/leu.2009.123

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  • Bortezomib, carfilzomib, and ixazomib are proteasome inhibitors.

    “Bortezomib, carfilzomib, and ixazomib are proteasome inhibitors.81–83”

    From Multiple myeloma: 2024 update on diagnosis, risk-stratification, and management (2024) · cites this paper as [83]

    The To the Editor section identifies bortezomib as an agent that inhibits the proteasome and explicitly calls carfilzomib a proteasome inhibitor. Our copy does not mention ixazomib, so it supports only two of the three identifications. (LLM, conf=0.88)

    Experimental — accuracy not yet measured

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Authors
Gutman, D., Morales, A. A., & Boise, L. H.
Affiliations
University of Miami (US)
Corresponding author
Boise, L H
Venue
Leukemia
Published
2009-06-11
Volume
23
Issue
11
Pages
2181-2183
ISSN
  • 0887-6924 (ISSN-L)
  • 1476-5551
OpenAlex
W2030885435
Cited by
53
References
8
Citations by year
2026: 1 · 2025: 2 · 2024: 1 · 2022: 3 · 2021: 1 · 2020: 4 · 2019: 3 · 2018: 4 · 2017: 6 · 2016: 4 · 2015: 2 · 2014: 5 · 2013: 6 · 2012: 7
FWCI
2.43
Type
journal article
Language
en
Open access
Locations
  • Leukemia (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Cancer Institute (R01CA127910)
Topics
  • Health Sciences › Medicine › Hematology › Multiple Myeloma Research and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
Keywords
multidrug resistance, proteasome inhibitors, multiple myeloma, carfilzomib, nelfinavir, lopinavir, PA28α
MeSH terms
Bortezomib, Boronic Acids, Humans, Multiple Myeloma, Oligopeptides, Phenotype, Protease Inhibitors, Pyrazines, Drug Resistance, Multiple, Cell Line, Tumor

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