小分子调节剂靶向Cullin-RING E3泛素连接酶4

Kenneth Wu, Benjamin D Hopkins, Roberto Sanchez, Robert J DeVita, Zhen-Qiang Pan
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引用次数: 0

摘要

Cullin-RING E3泛素连接酶4 (CRL4)在细胞周期进程中起重要作用。最近通过高通量筛选和后续先导研究,发现了抑制E3 CRL4核心连接酶复合物并具有抗癌潜力的小分子33-11和KH-4-43。本文综述:1)对E3 CRL4的结构组织、主要底物靶点及其在癌症中的作用进行了最新的研究;2)讨论了寻找CRL抑制剂的挑战和策略;3)总结已鉴定的CRL4抑制剂的特性,以及它们在探索CRL4生物学和作为治疗剂方面的潜在效用。
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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Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators.

Cullin-RING E3 ubiquitin ligase 4 (CRL4) plays an essential role in cell cycle progression. Recent efforts using high throughput screening and follow up hit-to-lead studies have led to identification of small molecules 33-11 and KH-4-43 that inhibit E3 CRL4's core ligase complex and exhibit anticancer potential. This review provides: 1) an updated perspective of E3 CRL4, including structural organization, major substrate targets and role in cancer; 2) a discussion of the challenges and strategies for finding the CRL inhibitor; and 3) a summary of the properties of the identified CRL4 inhibitors as well as a perspective on their potential utility to probe CRL4 biology and act as therapeutic agents.

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