小脑
泊马度胺
来那度胺
DNA连接酶
抗药性
泛素连接酶
多发性骨髓瘤
药理学
医学
癌症研究
生物
遗传学
DNA
泛素
基因
免疫学
作者
Holly Lee,Paola Neri,Nizar J. Bahlis
标识
DOI:10.1016/j.hoc.2024.01.001
摘要
Cereblon-targeting degraders, including immunomodulatory imide drugs lenalidomide and pomalidomide alongside cereblon E3 ligase modulators like iberdomide and mezigdomide, have demonstrated significant anti-myeloma effects. These drugs play a crucial role in diverse therapeutic approaches for multiple myeloma (MM), emphasizing their therapeutic importance across various disease stages. Despite their evident efficacy, approximately 5% to 10% of MM patients exhibit primary resistance to lenalidomide, and resistance commonly develops over time. Understanding the intricate mechanisms of action and resistance to this drug class becomes imperative for refining and advancing novel therapeutic combinations.
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