Wu Kenneth, Hopkins Benjamin D, Sanchez Roberto, DeVita Robert J, Pan Zhen-Qiang
Department of Oncological Sciences, The Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029-6574, USA.
Genetics and Genomics, The Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029-6574, USA.
J Cell Signal. 2021;2(3):195-205. doi: 10.33696/Signaling.2.051.
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 and 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.
Cullin-RING E3泛素连接酶4(CRL4)在细胞周期进程中起着至关重要的作用。最近通过高通量筛选以及后续从活性分子到先导化合物的研究工作,已鉴定出能够抑制E3 CRL4核心连接酶复合物并具有抗癌潜力的小分子。本综述提供了:1)E3 CRL4的最新观点,包括结构组成、主要底物靶点及其在癌症中的作用;2)关于寻找CRL抑制剂的挑战和策略的讨论;3)已鉴定出的CRL4抑制剂的特性总结以及对其在探索CRL4生物学特性和作为治疗药物方面潜在用途的展望。