Vicente André T S, Moura Sara P S P, Salvador Jorge A R
Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Coimbra, Coimbra, Portugal.
Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
Commun Chem. 2025 Jul 29;8(1):218. doi: 10.1038/s42004-025-01598-9.
PROteolysis-Targeting Chimeras (PROTACs) are an emerging class of molecules capable of inducing a forced approximation between a protein of interest (POI) and an E3 ligase enzyme (e.g., Cereblon), leading to the degradation of the POI by the cell's own machinery. Although in early stages of development, PROTACs' unique mechanisms of action offer a novel therapeutic strategy, which has attracted growing interest worldwide. Cereblon-based PROTACs are the most studied class of PROTACs and have been actively researched in recent years for the treatment of different diseases, from cancer to neurological disorders, with some of them already in clinical trials. In this review, we provide a comprehensive and critical analysis covering the recent advances, potential challenges and future prospects regarding the design and synthesis, as well as pre- and clinical evaluation of cereblon-based PROTACs. By integrating insights from drug discovery and development, a broad yet in-depth discussion is given to guide future research on cereblon-based PROTACs.
蛋白酶靶向嵌合体(PROTACs)是一类新兴的分子,能够促使目标蛋白(POI)与E3连接酶(如脑啡肽酶)之间发生强制接近,从而导致细胞自身机制将POI降解。尽管仍处于开发早期阶段,但PROTACs独特的作用机制提供了一种新的治疗策略,已在全球范围内引起越来越多的关注。基于脑啡肽酶的PROTACs是研究最多的一类PROTACs,近年来一直在积极研究用于治疗从癌症到神经疾病等不同疾病,其中一些已进入临床试验阶段。在本综述中,我们对基于脑啡肽酶的PROTACs的设计与合成以及临床前和临床评估的最新进展、潜在挑战和未来前景进行了全面且批判性的分析。通过整合药物发现与开发的见解,进行了广泛而深入的讨论,以指导未来对基于脑啡肽酶的PROTACs的研究。