Discovery of Novel PDEδ Autophagic Degraders: A Case Study of Autophagy-Tethering Compound (ATTEC)

被引:15
作者
Bao, Jingying [1 ,2 ]
Chen, Zhenqian [1 ,2 ]
Li, Yu [2 ]
Chen, Long [2 ]
Wang, Wei [2 ]
Sheng, Chunquan [2 ]
Dong, Guoqiang [2 ]
机构
[1] East China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China
[2] Second Mil Med Univ, Sch Pharm, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Targeted protein degradation; autophagy-tethering compound; PDE delta; KRAS; antitumor activity; TARGETED PROTEIN-DEGRADATION; KRAS;
D O I
10.1021/acsmedchemlett.3c00161
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The autophagy-tethering compound (ATTEC) technology has emerged as a promising strategy for targeted protein degradation (TPD). Here, we report the discovery of the first generation of PDE delta autophagic degraders using an ATTEC approach. The most promising compound 12c exhibited potent PDE delta binding affinity and efficiently induced PDE delta degradation in a concentration-dependent manner. Mechanistic studies confirmed that compound 12c reduced the PDE delta protein level through lysosome-mediated autophagy without affecting the PDE delta mRNA expression. Importantly, compound 12c was much more effective in suppressing the growth in KRAS mutant pancreatic cancer cells than the corresponding PDE delta inhibitor. Taken together, this study expands the application scope of the ATTEC approach and highlights the effectiveness of the PDE delta autophagic degradation strategy in antitumor drug discovery.
引用
收藏
页码:29 / 35
页数:7
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