化学
工具箱
泛素连接酶
计算生物学
天然产物
蛋白质降解
纳米技术
泛素
生物化学
生物
计算机科学
基因
材料科学
程序设计语言
作者
Cheng Chen,Yanyan Feng,Chen Zhou,Zhouyan Liu,Ziwei Tang,Qian Zhang,Tong Li,Chenglei Gu,Jichao Chen
标识
DOI:10.1016/j.bioorg.2024.107772
摘要
Targeted protein degradation (TPD) has emerged as a powerful approach for eliminating cancer-causing proteins through an "event-driven" pharmacological mode. Proteolysis-targeting chimeras (PROTACs), molecular glues (MGs), and hydrophobic tagging (HyTing) have evolved into three major classes of TPD technologies. Natural products (NPs) are a primary source of anticancer drugs and have played important roles in the development of TPD technology. NPs potentially expand the toolbox of TPD by providing a variety of E3 ligase ligands, protein of interest (POI) warheads, and hydrophobic tags (HyTs). As a promising direction in the TPD field, NP-based degraders have shown great potential for anticancer therapy. In this review, we summarize recent advances in the development of NP-based degraders (PROTACs, MGs and HyTing) with anticancer applications. Moreover, we put forward the challenges while presenting potential opportunities for the advancement of future targeted protein degraders derived from NPs.
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