Development and therapeutic potential of GSPT1 molecular glue degraders: A medicinal chemistry perspective

被引:1
|
作者
Chang, Xiujin [1 ]
Qu, Fangui [1 ]
Li, Chunxiao [1 ]
Zhang, Jingtian [1 ]
Zhang, Yanqing [1 ]
Xie, Yuanyuan [1 ]
Fan, Zhongpeng [1 ]
Bian, Jinlei [1 ]
Wang, Jubo [1 ,2 ]
Li, Zhiyu [1 ,2 ]
Xu, Xi [1 ,2 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Dept Med Chem, Nanjing, Peoples R China
[2] China Pharmaceut Univ, Sch Pharm, Dept Med Chem, Nanjing 211100, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
GSPT1; molecular glue; structure-activity relationships; targeted protein degradation; translation termination; RELEASE FACTOR ERF1; TERMINATION FACTOR ERF1; STOP CODON RECOGNITION; PREGNANE-X-RECEPTOR; TRANSLATION TERMINATION; MESSENGER-RNA; IN-VIVO; DIFFERENTIAL EXPRESSION; SELECTIVE DEGRADATION; PROTEIN-DEGRADATION;
D O I
10.1002/med.22024
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Unprecedented therapeutic targeting of previously undruggable proteins has now been achieved by molecular-glue-mediated proximity-induced degradation. As a small GTPase, G1 to S phase transition 1 (GSPT1) interacts with eRF1, the translation termination factor, to facilitate the process of translation termination. Studied demonstrated that GSPT1 plays a vital role in the acute myeloid leukemia (AML) and MYC-driven lung cancer. Thus, molecular glue (MG) degraders targeting GSPT1 is a novel and promising approach for treating AML and MYC-driven cancers. In this Perspective, we briefly summarize the structural and functional aspects of GSPT1, highlighting the latest advances and challenges in MG degraders, as well as some representative patents. The structure-activity relationships, mechanism of action and pharmacokinetic features of MG degraders are emphasized to provide a comprehensive compendium on the rational design of GSPT1 MG degraders. We hope to provide an updated overview, and design guide for strategies targeting GSPT1 for the treatment of cancer.
引用
收藏
页码:1727 / 1767
页数:41
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