具有治疗活性的类黄酮化E2s抑制剂的发现。

IF 5.9 2区 医学 Q1 ONCOLOGY Oncogenesis Pub Date : 2023-09-16 DOI:10.1038/s41389-023-00490-2
Maa Mamun, Ying Liu, Yin-Ping Geng, Yi-Chao Zheng, Ya Gao, Jian-Gang Sun, Long-Fei Zhao, Li-Juan Zhao, Hong-Min Liu
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引用次数: 0

摘要

类化修饰是神经前体细胞表达发育下调8 (NEDD8)的单体或聚合物向底物的书写。为了发生类化修饰,需要三种酶:激活剂(E1),共轭剂(E2)和结扎剂(E3)。然而,泛素偶联酶E2M (UBE2M)和E2F (UBE2F)起着核心作用,它们是E2酶家族的一部分。最近对这两种蛋白的结构和机制的了解,有助于深入了解它们在细胞凋亡、细胞周期阻滞和基因组稳定性方面的生理作用。因此,为了治疗癌症,开发新的抑制UBE2M或UBE2F与E1或E3相互作用的抑制剂是很有吸引力的。在这篇评价中,我们总结了E2与E1和E3相互作用的现有认识,并展望了利用类化修饰E2作为开发新的抗癌药物的药理学靶点的前景。
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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Discovery of neddylation E2s inhibitors with therapeutic activity.

Neddylation is the writing of monomers or polymers of neural precursor cells expressed developmentally down-regulated 8 (NEDD8) to substrate. For neddylation to occur, three enzymes are required: activators (E1), conjugators (E2), and ligators (E3). However, the central role is played by the ubiquitin-conjugating enzymes E2M (UBE2M) and E2F (UBE2F), which are part of the E2 enzyme family. Recent understanding of the structure and mechanism of these two proteins provides insight into their physiological effects on apoptosis, cell cycle arrest and genome stability. To treat cancer, it is therefore appealing to develop novel inhibitors against UBE2M or UBE2F interactions with either E1 or E3. In this evaluation, we summarized the existing understanding of E2 interaction with E1 and E3 and reviewed the prospective of using neddylation E2 as a pharmacological target for evolving new anti-cancer remedies.

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来源期刊
Oncogenesis
Oncogenesis ONCOLOGY-
CiteScore
11.90
自引率
0.00%
发文量
70
审稿时长
26 weeks
期刊介绍: Oncogenesis is a peer-reviewed open access online journal that publishes full-length papers, reviews, and short communications exploring the molecular basis of cancer and related phenomena. It seeks to promote diverse and integrated areas of molecular biology, cell biology, oncology, and genetics.
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