表观遗传学
透视图(图形)
髓系白血病
机制(生物学)
钥匙(锁)
疾病
医学
恶性疾病
后生
风险分析(工程)
白血病
计算生物学
DNA甲基化
髓系细胞
业务
髓样
滑膜肉瘤
政治学
转化(遗传学)
癌症研究
鉴定(生物学)
生物
计算机科学
作者
Eleonora Boccia,Stefania Terracciano,Maria Giovanna Chini,Giuseppe Bifulco,Gianluigi Lauro
标识
DOI:10.1080/13543776.2025.2606811
摘要
The patent landscape reflects a growing interest in BRD9 as an epigenetic target for its key role in various pathologies. The recent patent data show how selective BRD9 degraders represent a significant step forward in terms of efficacy and selectivity, with promising results in preclinical models of acute myeloid leukemia (AML), synovial sarcoma (SS), and Huntington's disease (HD). Despite several critical issues, the selective degradation of this epigenetic target shows great potential to be an innovative therapeutic strategy.
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