整合素
泛素连接酶
化学
胶水
天然产物
泛素
体外
跨膜蛋白
细胞生物学
癌症研究
高通量筛选
表型
小分子
计算生物学
受体
基质金属蛋白酶
细胞
DNA连接酶
分子生物学
药物发现
作者
Wei Gong,Di Yang,Junrui Tian,Yufei Chai,Tiantian Yu,Qingnan Wu,Yan Wang,Weimin Zhang,Qimin Zhan
标识
DOI:10.1002/advs.202515970
摘要
ABSTRACT Integrin β 4 (gene name: ITGB4) overexpression is associated with aggressive phenotypes and poor prognosis across multiple solid tumors. Despite its clinical significance, therapeutic strategies targeting integrin β 4 remain underdeveloped. Targeted protein degradation technology, particularly molecular glue degraders, offer a promising approach for eliminating oncoproteins. However, the serendipitous discovery of molecular glues and limited exploration of substrate receptor have largely hindered the rational development of molecular glue degraders. In this study, through high throughput screening from a natural product library, we identified halofuginone (HF) as a potential molecular glue that promotes integrin β 4 degradation via the CRL4B WDR18 E3 ubiquitin ligase complex. HF administration markedly disrupted the aggressive progression of tumor cell both in vitro and in vivo. In summary, our study not only establishes HF as a promising degrader of integrin β 4 but also demonstrates the utility of natural product screening for discovering molecular glue degraders, providing a novel therapeutic strategy for targeting oncogenic transmembrane proteins.
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