Targeting Oncogene mRNA Translation in B-Cell Malignancies with eFT226, a Potent and Selective Inhibitor of eIF4A-Reference-Cited by-同舟云学术

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Targeting Oncogene mRNA Translation in B-Cell Malignancies with eFT226, a Potent and Selective Inhibitor of eIF4A

Published:2020-10-09 Issue:1 Volume:20 Page:26-36
ISSN:1535-7163
Container-title:Molecular Cancer Therapeutics
language:en
Short-container-title:Mol Cancer Ther

Author:

Thompson Peggy A.,Eam Boreth,Young Nathan P.,Fish Sarah,Chen Joan,Barrera Maria,Howard Haleigh,Sung Eric,Parra Ana,Staunton Jocelyn,Chiang Gary G.^ORCID,Gerson-Gurwitz Adina,Wegerski Christopher J.,Nevarez Andres,Clarine Jeff,Sperry Samuel,Xiang Alan,Nilewski Christian^ORCID,Packard Garrick K.,Michels Theodore^ORCID,Tran Chinh,Sprengeler Paul A.,Ernst Justin T.,Reich Siegfried H.,Webster Kevin R.

Funder

eFFECTOR Therapeutics

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Cited by 37 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. DMDA-PatA mediates RNA sequence-selective translation repression by anchoring eIF4A and DDX3 to GNG motifs;Nature Communications;2024-09-02

2. The crosstalk between metabolism and translation;Cell Metabolism;2024-09

3. The shaping of mRNA translation plasticity by RNA G-quadruplexes in cancer progression and therapy resistance;NAR Cancer;2024-04-08

4. RNA helicase EIF4A1-mediated translation is essential for the GC response;Life Science Alliance;2023-11-27

5. eIF4A1 is essential for reprogramming the translational landscape of Wnt-driven colorectal cancers;2023-11-13

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