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2000
Volume 28, Issue 24
  • ISSN: 0929-8673
  • E-ISSN: 1875-533X

Abstract

The PROTAC (PROteolysis TArgeting Chimera) technology is a target protein degradation strategy, based on the ubiquitin-proteasome system, which has been gradually developed into a potential means of targeted cancer therapy in recent years. This strategy has already shown significant advantages over traditional small-molecule inhibitors in terms of pharmacodynamics, selectivity, and drug resistance. Several small molecule PROTACs have been in Phase I clinical trial. Herein, we have introduced the mechanism, characteristics, and advantages of PROTAC strategy. And we have summarized the recent advances in the development of small-molecule PROTACs for cancer treatment. We hope this review will be helpful in optimizing the design of the ideal small- molecule PROTACs and advancing targeted anticancer research.

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/content/journals/cmc/10.2174/0929867327666201117141611
2021-07-01
2025-04-13
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/content/journals/cmc/10.2174/0929867327666201117141611
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  • Article Type:
    Review Article
Keyword(s): Anticancer; E3 ligase; ligand; PROTAC; protein degradation; transduction; ubiquitination
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