| Literature DB >> 33160761 |
Shenxin Zeng1, Wenhai Huang1, Xiaoliang Zheng2, Zhimin Zhang3, Jian Wang4, Zhengrong Shen5.
Abstract
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.Entities:
Keywords: Drug discovery; Drug resistance; PROTAC; Small molecule; Target protein degradation; Undruggable target
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Year: 2020 PMID: 33160761 DOI: 10.1016/j.ejmech.2020.112981
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514