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儿科临床前试验计划对 NEDD8-激活酶抑制剂 MLN4924 的初步测试。

Initial testing of the investigational NEDD8-activating enzyme inhibitor MLN4924 by the pediatric preclinical testing program.

机构信息

Cancer Therapy Evaluation Program, NCI, Bethesda, Maryland 20892, USA.

出版信息

Pediatr Blood Cancer. 2012 Aug;59(2):246-53. doi: 10.1002/pbc.23357. Epub 2011 Oct 19.

Abstract

BACKGROUND

MLN4924 is an investigational first-in-class small molecule inhibitor of NEDD8-activating enzyme (NAE). NAE is an essential component of the NEDD8 conjugation pathway, controlling the activity of a subset of ubiquitin-proteasome system (UPS) E3 ligases, multiprotein complexes that transfer ubiquitin molecules to substrate proteins.

PROCEDURES

MLN4924 was tested against the PPTP in vitro panel using 96-hour exposure time at concentrations ranging from 1.0 nM to 10 µM. It was tested in vivo at a dose of 100 mg/kg [66 mg/kg for the acute lymphoblastic leukemia (ALL) xenografts] administered orally twice daily × 5 days. Treatment duration was 3 weeks.

RESULTS

The median relative IC(50) for MLN4924 against the PPTP cell lines was 143 nM, (range: 15-678 nM) with that for the Ewing panel being significantly lower (31 nM). MLN4924 induced significant differences in EFS distribution compared to control in 20 of 34 (59%) evaluable solid tumor xenografts. MLN4924 induced intermediate activity (EFS T/C values >2) in 9 of the 33 evaluable xenografts (27%), including 4 of 4 glioblastoma xenografts, 2 of 3 Wilm's tumor xenografts, 2 of 5 rhabdomyosarcoma xenografts, and 1 of 4 neuroblastoma xenografts. For the ALL panel, 5 of 8 evaluable xenografts showed intermediate activity for the EFS T/C measure. MLN4924 did not induce objective responses in the PPTP solid tumor or ALL panels.

CONCLUSIONS

MLN4924 showed potent activity in vitro and in vivo showed tumor growth inhibitory activity against a subset of the PPTP solid tumor and ALL xenografts.

摘要

背景

MLN4924 是一种首创的小分子 NEDD8 激活酶 (NAE) 抑制剂。NAE 是 NEDD8 缀合途径的一个重要组成部分,控制着一组泛素-蛋白酶体系统 (UPS) E3 连接酶的活性,这些多蛋白复合物将泛素分子转移到底物蛋白上。

程序

使用 96 小时的暴露时间,在 1.0 nM 至 10 μM 的浓度范围内,将 MLN4924 针对 PPTP 体外面板进行测试。以 100 mg/kg 的剂量 [急性淋巴细胞白血病 (ALL) 异种移植物为 66 mg/kg] 口服给药,每天两次,连续 5 天。治疗持续时间为 3 周。

结果

MLN4924 对 PPTP 细胞系的中位相对 IC(50)为 143 nM(范围:15-678 nM),而 Ewing 面板的 IC(50)明显更低(31 nM)。与对照组相比,MLN4924 在 34 个可评估的实体瘤异种移植物中的 20 个(59%)中诱导 EFS 分布的显著差异。在 33 个可评估的异种移植物中,MLN4924 诱导中间活性(EFS T/C 值>2)的有 9 个(27%),包括 4 个神经胶质瘤异种移植物、3 个肾母细胞瘤异种移植物、5 个横纹肌肉瘤异种移植物中的 2 个和 4 个神经母细胞瘤异种移植物中的 1 个。对于 ALL 面板,8 个可评估的异种移植物中有 5 个对 EFS T/C 测量显示出中间活性。MLN4924 在 PPTP 实体瘤或 ALL 面板中均未诱导客观反应。

结论

MLN4924 在体外显示出强大的活性,体内显示出针对 PPTP 实体瘤和 ALL 异种移植物的肿瘤生长抑制活性。

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