帕纳替尼
髓系白血病
抗药性
癌症研究
突变体
突变
后天抵抗
变构调节
医学
药理学
生物
达沙替尼
伊马替尼
遗传学
内科学
受体
基因
作者
Christopher A. Eide,Diana Brewer,Tao Xie,Anna Reister Schultz,Samantha L. Savage,Serena Muratcioğlu,Noah Merz,Richard D. Press,Thomas O’Hare,Thomas Jacob,Tania Q. Vu,Cristina E. Tognon,Tara A. Macey,John Kuriyan,Charalampos G. Kalodimos,Brian J. Druker
出处
期刊:Cancer Cell
[Elsevier]
日期:2024-08-29
卷期号:42 (9): 1486-1488
标识
DOI:10.1016/j.ccell.2024.08.004
摘要
BCR-ABL1 compound mutations can lead to resistance to ABL1 inhibitors in chronic myeloid leukemia (CML), which could be targeted by combining the ATP-site inhibitor ponatinib and the allosteric inhibitor asciminib. Here, we report the clinical validation of this approach in a CML patient, providing a basis for combination therapy to overcome such resistance.
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