M3258 Is a Selective Inhibitor of the Immunoproteasome Subunit LMP7 (β5i) Delivering Efficacy in Multiple Myeloma Models-Reference-Cited by-同舟云学术

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M3258 Is a Selective Inhibitor of the Immunoproteasome Subunit LMP7 (β5i) Delivering Efficacy in Multiple Myeloma Models

Published:2021-05-27 Issue:8 Volume:20 Page:1378-1387
ISSN:1535-7163
Container-title:Molecular Cancer Therapeutics
language:en
Short-container-title:Mol Cancer Ther

Author:

Sanderson Michael P.,Friese-Hamim Manja,Walter-Bausch Gina,Busch Michael,Gaus Stefanie,Musil Djordje,Rohdich Felix,Zanelli Ugo,Downey-Kopyscinski Sondra L.,Mitsiades Constantine S.,Schadt Oliver,Klein Markus,Esdar Christina

Funder

Merck KGaA, Darmstadt, Germany

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Targeting the ubiquitin pathway in lymphoid malignancies;Cancer Letters;2024-07

2. Development of Proteasome Inhibitors for Cancer Therapy;International Journal of Drug Discovery and Pharmacology;2024-03-18

3. Interplay between proteasome inhibitors and NF-κB pathway in leukemia and lymphoma: a comprehensive review on challenges ahead of proteasome inhibitors;Cell Communication and Signaling;2024-02-08

4. Structures revealing mechanisms of resistance and collateral sensitivity of Plasmodium falciparum to proteasome inhibitors;Nature Communications;2023-12-14

5. Immunoproteasome function maintains oncogenic gene expression in KMT2A-complex driven leukemia;Molecular Cancer;2023-12-04

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