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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.

DOI:10.1002/pbc.23357
PMID:22012946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3823062/
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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/8fac173c615b/nihms322795f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/65d94f9b8c49/nihms322795f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/bcd0d253f874/nihms322795f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/df99ee8d7179/nihms322795f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/8fac173c615b/nihms322795f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/65d94f9b8c49/nihms322795f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/bcd0d253f874/nihms322795f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/df99ee8d7179/nihms322795f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb2/3823062/8fac173c615b/nihms322795f4.jpg

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本文引用的文献

1
Guidelines for accurate EC50/IC50 estimation.准确估算EC50/IC50的指南。
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2
Inhibition of NEDD8-activating enzyme induces rereplication and apoptosis in human tumor cells consistent with deregulating CDT1 turnover.NEDD8-激活酶抑制诱导人肿瘤细胞的复制再启动和凋亡,与 CDT1 周转的失调一致。
Cancer Res. 2011 Apr 15;71(8):3042-51. doi: 10.1158/0008-5472.CAN-10-2122. Epub 2011 Apr 12.
3
NEDD8-targeting drug MLN4924 elicits DNA rereplication by stabilizing Cdt1 in S phase, triggering checkpoint activation, apoptosis, and senescence in cancer cells.
MYOD-SKP2 axis boosts tumorigenesis in fusion negative rhabdomyosarcoma by preventing differentiation through p57 targeting.
MYOD-SKP2 轴通过靶向 p57 防止分化来促进融合阴性横纹肌肉瘤的肿瘤发生。
Nat Commun. 2023 Dec 15;14(1):8373. doi: 10.1038/s41467-023-44130-0.
4
The Anti-Tumor Activity of the NEDD8 Inhibitor Pevonedistat in Neuroblastoma.PEVONEDISTAT 对神经母细胞瘤的抗肿瘤活性。
Int J Mol Sci. 2021 Jun 18;22(12):6565. doi: 10.3390/ijms22126565.
5
Neddylation of sterol regulatory element-binding protein 1c is a potential therapeutic target for nonalcoholic fatty liver treatment.固醇调节元件结合蛋白 1c 的 Neddylation 是治疗非酒精性脂肪肝的潜在治疗靶点。
Cell Death Dis. 2020 Apr 24;11(4):283. doi: 10.1038/s41419-020-2472-6.
6
The NEDD8-activating enzyme inhibitor MLN4924 induces DNA damage in Ph+ leukemia and sensitizes for ABL kinase inhibitors.NEDD8 激活酶抑制剂 MLN4924 诱导 Ph+ 白血病中的 DNA 损伤,并增强对 ABL 激酶抑制剂的敏感性。
Cell Cycle. 2019 Sep;18(18):2307-2322. doi: 10.1080/15384101.2019.1646068. Epub 2019 Jul 26.
7
Blocking PD1/PDL1 Interactions Together with MLN4924 Therapy is a Potential Strategy for Glioma Treatment.阻断PD1/PDL1相互作用并联合MLN4924治疗是胶质瘤治疗的一种潜在策略。
J Cancer Sci Ther. 2018;10(8):190-197. doi: 10.4172/1948-5956.1000543. Epub 2018 Aug 6.
8
A review of new agents evaluated against pediatric acute lymphoblastic leukemia by the Pediatric Preclinical Testing Program.儿科临床前试验计划评估的针对小儿急性淋巴细胞白血病的新药物的综述。
Leukemia. 2016 Nov;30(11):2133-2141. doi: 10.1038/leu.2016.192. Epub 2016 Jul 15.
9
A phase I study of the investigational NEDD8-activating enzyme inhibitor pevonedistat (TAK-924/MLN4924) in patients with metastatic melanoma.一项关于研究性NEDD8激活酶抑制剂pevonedistat(TAK-924/MLN4924)用于转移性黑色素瘤患者的I期研究。
Invest New Drugs. 2016 Aug;34(4):439-49. doi: 10.1007/s10637-016-0348-5. Epub 2016 Apr 8.
10
PPARγ neddylation essential for adipogenesis is a potential target for treating obesity.对脂肪生成至关重要的PPARγ 泛素化是治疗肥胖症的一个潜在靶点。
Cell Death Differ. 2016 Aug;23(8):1296-311. doi: 10.1038/cdd.2016.6. Epub 2016 Mar 18.
NEDD8 靶向药物 MLN4924 通过稳定 S 期的 Cdt1 引发 DNA 再复制,从而激活检查点、诱导癌细胞凋亡和衰老。
Cancer Res. 2010 Dec 15;70(24):10310-20. doi: 10.1158/0008-5472.CAN-10-2062.
4
MLN4924, a NEDD8-activating enzyme inhibitor, is active in diffuse large B-cell lymphoma models: rationale for treatment of NF-{kappa}B-dependent lymphoma.MLN4924,一种 NEDD8 激活酶抑制剂,在弥漫性大 B 细胞淋巴瘤模型中具有活性:治疗 NF-κB 依赖性淋巴瘤的原理。
Blood. 2010 Sep 2;116(9):1515-23. doi: 10.1182/blood-2010-03-272567. Epub 2010 Jun 4.
5
Aggressive lymphomas.侵袭性淋巴瘤。
N Engl J Med. 2010 Apr 15;362(15):1417-29. doi: 10.1056/NEJMra0807082.
6
Inhibition of NEDD8-activating enzyme: a novel approach for the treatment of acute myeloid leukemia.抑制 NEDD8-激活酶:治疗急性髓系白血病的新方法。
Blood. 2010 May 6;115(18):3796-800. doi: 10.1182/blood-2009-11-254862. Epub 2010 Mar 4.
7
Substrate-assisted inhibition of ubiquitin-like protein-activating enzymes: the NEDD8 E1 inhibitor MLN4924 forms a NEDD8-AMP mimetic in situ.底物辅助的泛素样蛋白激活酶抑制:NEDD8 E1 抑制剂 MLN4924 在原位形成 NEDD8-AMP 类似物。
Mol Cell. 2010 Jan 15;37(1):102-11. doi: 10.1016/j.molcel.2009.12.024.
8
Constitutive NF-kappaB activity regulates the expression of VEGF and IL-8 and tumor angiogenesis of human glioblastoma.组成型 NF-κB 活性调节人胶质母细胞瘤中 VEGF 和 IL-8 的表达和肿瘤血管生成。
Oncol Rep. 2010 Mar;23(3):725-32.
9
Chronic active B-cell-receptor signalling in diffuse large B-cell lymphoma.弥漫性大 B 细胞淋巴瘤中慢性活性 B 细胞受体信号转导。
Nature. 2010 Jan 7;463(7277):88-92. doi: 10.1038/nature08638.
10
TNFAIP3/A20 functions as a novel tumor suppressor gene in several subtypes of non-Hodgkin lymphomas.TNFAIP3/A20在几种非霍奇金淋巴瘤亚型中作为一种新的肿瘤抑制基因发挥作用。
Blood. 2009 Sep 17;114(12):2467-75. doi: 10.1182/blood-2008-12-194852. Epub 2009 Jul 16.