CRBN-PROTACs 在癌症治疗中的应用:从机理认识到临床应用。

IF 3.2 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Chemical Biology & Drug Design Pub Date : 2024-11-04 DOI:10.1111/cbdd.70009
Riya Thapa, Asif Ahmad Bhat, Gaurav Gupta, S. Renuka Jyothi, Irwanjot Kaur, Sachin Kumar, Naveen Sharma, G. V. Siva Prasad, Atreyi Pramanik, Haider Ali
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引用次数: 0

摘要

Cereblon(CRBN)是E3泛素连接酶复合物的一个成员,它作为癌症治疗靶点已引起了广泛关注。CRBN 在癌症进展过程中调节各种蛋白质的降解,包括转录因子和信号分子。PROTAC(蛋白分解靶向嵌合体)是一种利用细胞降解系统选择性清除致病蛋白的新方法。依赖 CRBN 的 PROTAC 通过标记有害蛋白质,使其通过泛素-蛋白酶体系统被破坏。与传统的蛋白质抑制方法相比,这种策略具有多种优势,包括克服耐药性的潜力。最近在开发基于 CRBN 的 PROTACs 方面取得的进展显示,在血液恶性肿瘤和实体瘤的临床前研究中都取得了可喜的成果。此外,基于 CRBN 的 PROTACs 还增进了我们对 CRBN 在癌症中作用的了解,有可能成为患者分层和预测治疗反应的生物标志物。在这篇综述中,我们阐述了依赖 CRBN 的 PROTACs(CRBN-PROTACs)的作用机制,总结了临床前和临床应用的最新进展,并提供了我们对未来发展的展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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CRBN-PROTACs in Cancer Therapy: From Mechanistic Insights to Clinical Applications

Cereblon (CRBN), a member of the E3 ubiquitin ligase complex, has gained significant attention as a therapeutic target in cancer. CRBN regulates the degradation of various proteins in cancer progression, including transcription factors and signaling molecules. PROTACs (proteolysis-targeting chimeras) are a novel approach that uses the cell's degradation system to remove disease-causing proteins selectively. CRBN-dependent PROTACs work by tagging harmful proteins for destruction through the ubiquitin–proteasome system. This strategy offers several advantages over traditional protein inhibition methods, including the potential to overcome drug resistance. Recent progress in developing CRBN-based PROTACs has shown promising preclinical results in both hematologic malignancies and solid tumors. Additionally, CRBN-based PROTACs have enhanced our understanding of CRBN's role in cancer, potentially serving as biomarkers for patient stratification and predicting therapeutic responses. In this review, we delineate the mechanisms of action for CRBN-dependent PROTACs (CRBN-PROTACs), summarize recent advances in preclinical and clinical applications, and provide our perspective on future development.

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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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