癌症研究
转录因子
泛素
生物
髓系白血病
髓样
平方毫米
HEK 293细胞
下调和上调
细胞培养
蛋白质降解
细胞生长
细胞生物学
突变体
靶向治疗
癌基因
白血病
程序性细胞死亡
运行x1
蛋白酶体
信号转导
蛋白质水解
细胞
抄写(语言学)
小分子
细胞凋亡
泛素连接酶
化学
核蛋白
清脆的
作者
Evie Rigby,Francesca Fasanella Masci,Akshara Narayanan,Elżbieta Kania,John A. Harris,Jamie J.L. Williams,Binghua Zhang,Lijun Liu,Laura Richmond,Fengtao Zhou,Ke Ding,Ruaidhrı́ J. Carmody,Patrick A. Eyers,Karen Keeshan
摘要
The myeloid oncogene TRIB2 is a key driver of acute myeloid leukaemia (AML) pathogenesis, promoting chemoresistance and blocking differentiation through ubiquitin-mediated degradation of the C/EBPα transcription factor. Despite its stable and sometimes elevated expression across AML subtypes, TRIB2 remains a clinically untargeted vulnerability. Here, we present a comprehensive investigation into TRIB2 degradation mechanisms using multimodal approaches, including CRISPR knockout, mutational protein stability, small molecule TRIB2 engagement, and evaluation of a novel targeted protein degrader (TRIB2-PROTAC). We identify afatinib, a multi-ERBB covalent inhibitor, as a rapid inducer of TRIB2 degradation, triggering AML cell death potentially via signalling pathways distinct from ERBB. Importantly, TRIB2 degradation synergised with cytarabine, the frontline AML chemotherapy, amplifying therapeutic efficacy. Mapping of TRIB2 ubiquitination sites revealed Lys-63 as critical for its own proteolytic turnover, and a Lys-to-Arg degradation-resistant mutant (KallR) conferred enhanced chemoresistance and increased leukaemic engraftment in vivo. CRISPR-mediated TRIB2 knockout validated an essential role in AML cell survival. Consistently, the novel TRIB2-PROTAC (compound 5K) achieved robust TRIB2 degradation and AML cell killing at low micromolar concentrations. These findings establish TRIB2 as a compelling therapeutic target in AML and demonstrate that leveraging the ubiquitin-proteasome system to degrade TRIB2 offers a promising strategy to overcome chemoresistance. The present work provides strong preclinical rationale for the development of TRIB2-targeting therapies in AML.
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