一种NEDD8激活酶抑制剂作为治疗癌症的新方法。

An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer.

作者信息

Soucy Teresa A, Smith Peter G, Milhollen Michael A, Berger Allison J, Gavin James M, Adhikari Sharmila, Brownell James E, Burke Kristine E, Cardin David P, Critchley Stephen, Cullis Courtney A, Doucette Amanda, Garnsey James J, Gaulin Jeffrey L, Gershman Rachel E, Lublinsky Anna R, McDonald Alice, Mizutani Hirotake, Narayanan Usha, Olhava Edward J, Peluso Stephane, Rezaei Mansoureh, Sintchak Michael D, Talreja Tina, Thomas Michael P, Traore Tary, Vyskocil Stepan, Weatherhead Gabriel S, Yu Jie, Zhang Julie, Dick Lawrence R, Claiborne Christopher F, Rolfe Mark, Bolen Joseph B, Langston Steven P

机构信息

Discovery, Millennium Pharmaceuticals, Inc., 40 Landsdowne Street, Cambridge, Massachusetts 02139, USA.

出版信息

Nature. 2009 Apr 9;458(7239):732-6. doi: 10.1038/nature07884.

Abstract

The clinical development of an inhibitor of cellular proteasome function suggests that compounds targeting other components of the ubiquitin-proteasome system might prove useful for the treatment of human malignancies. NEDD8-activating enzyme (NAE) is an essential component of the NEDD8 conjugation pathway that controls the activity of the cullin-RING subtype of ubiquitin ligases, thereby regulating the turnover of a subset of proteins upstream of the proteasome. Substrates of cullin-RING ligases have important roles in cellular processes associated with cancer cell growth and survival pathways. Here we describe MLN4924, a potent and selective inhibitor of NAE. MLN4924 disrupts cullin-RING ligase-mediated protein turnover leading to apoptotic death in human tumour cells by a new mechanism of action, the deregulation of S-phase DNA synthesis. MLN4924 suppressed the growth of human tumour xenografts in mice at compound exposures that were well tolerated. Our data suggest that NAE inhibitors may hold promise for the treatment of cancer.

摘要

细胞蛋白酶体功能抑制剂的临床研究表明,靶向泛素 - 蛋白酶体系统其他组分的化合物可能对治疗人类恶性肿瘤有效。NEDD8激活酶(NAE)是NEDD8缀合途径的一个重要组分,该途径控制泛素连接酶的cullin-RING亚型的活性,从而调节蛋白酶体上游一部分蛋白质的周转。cullin-RING连接酶的底物在与癌细胞生长和存活途径相关的细胞过程中起重要作用。在此,我们描述了MLN4924,一种有效的、选择性的NAE抑制剂。MLN4924通过一种新的作用机制——S期DNA合成失调,破坏cullin-RING连接酶介导的蛋白质周转,导致人肿瘤细胞凋亡死亡。在小鼠中,MLN4924在具有良好耐受性的化合物暴露水平下抑制了人肿瘤异种移植物的生长。我们的数据表明,NAE抑制剂可能在癌症治疗方面具有前景。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索