Proteolysis targeting chimera (PROTAC) in drug discovery paradigm: Recent progress and future challenges

被引:125
|
作者
Zeng, Shenxin [1 ,2 ]
Huang, Wenhai [1 ,2 ]
Zheng, Xiaoliang [3 ]
Cheng, Liyan [3 ]
Zhang, Zhimin [4 ]
Wang, Jian [2 ]
Shen, Zhengrong [1 ,2 ]
机构
[1] Hangzhou Med Coll, Inst Mat Med, Key Lab Neuropsychiat Drug Res Zhejiang Prov, Hangzhou 310013, Peoples R China
[2] Hangzhou Med Coll, Sch Pharm, Hangzhou 310013, Peoples R China
[3] Hangzhou Med Coll, Ctr Mol Med, Hangzhou 310013, Peoples R China
[4] HangZhou ZhongMei HuaDong Pharmaceut CO LTD, Dept Drug Platform Small Mol, 866 Moganshan Rd, Hangzhou 310011, Peoples R China
关键词
PROTAC; Small molecule; Target protein degradation; Undruggable target; Drug resistance; Drug discovery; INDUCED PROTEIN-DEGRADATION; SMALL-MOLECULE PROTACS; CELL LUNG-CANCER; HIGHLY POTENT; COVALENT INHIBITOR; BCR-ABL; AMG; 510; KINASE; DESIGN; DEGRADER;
D O I
10.1016/j.ejmech.2020.112981
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Proteolysis targeting chimera (PROTAC), hijacking protein of interest (POI) and recruiting E3 ligase for target degradation via the ubiquitin-proteasome pathway, is a novel drug discovery paradigm which has been widely used as biological tools and medicinal molecules with the potential of clinical application value. Currently, ARV-110, an orally small molecule PROTAC was designed to specifically target Androgen receptor (AR), firstly enters clinical phase I trials for the treatment of metastatic castration-resistant prostate cancer, which turns a new avenue for the development of PROTAC. We herein provide a detail summary on the latest one year progress of PROTAC target various proteins and elucidate the advantages of PROTAC technology. Finally, the potential challenges of this vibrant field are also discussed. (C) 2020 Elsevier Masson SAS. All rights reserved.
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页数:23
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