药物发现
效应器
计算生物学
癌细胞
生物
药品
癌症
癌症研究
生物信息学
细胞生物学
药理学
遗传学
作者
Zonghui Ma,Andrew A. Bolinger,Jia Zhou
标识
DOI:10.1016/j.drudis.2023.103774
摘要
Regulated induced proximity targeting chimeras (RIPTACs), a new class of heterobifunctional molecules, show promise in specifically targeting and eliminating cancer cells while leaving healthy cells unharmed. As a groundbreaking drug discovery approach, RIPTACs work by forming a stable complex with two proteins, one specifically found in cancer cells (target protein, TP) and the other pan-essential for cell survival (effector protein, EP), selectively disrupting the function of the EP in cancer cells and causing cell death. Interestingly, the TPs need not be linked to disease progression, broadening the spectrum of potential drug targets. This review summarizes the discovery and recent advances of the RIPTAC strategy. Additionally, it discusses the associated opportunities and challenges as well as future perspectives in this field.
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