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Phase I evaluation of XL019, an oral, potent, and selective JAK2 inhibitor.XL019 是一种口服、强效、选择性 JAK2 抑制剂的 I 期评估。
Leuk Res. 2014 Mar;38(3):316-22. doi: 10.1016/j.leukres.2013.12.006. Epub 2013 Dec 11.
2
Effect of AZD1480 in an epidermal growth factor receptor-driven lung cancer model.AZD1480 在表皮生长因子受体驱动的肺癌模型中的作用。
Lung Cancer. 2014 Jan;83(1):30-6. doi: 10.1016/j.lungcan.2013.10.011. Epub 2013 Oct 29.
3
The Janus kinases inhibitor AZD1480 attenuates growth of small cell lung cancers in vitro and in vivo.Janus 激酶抑制剂 AZD1480 可抑制小细胞肺癌的体外和体内生长。
Clin Cancer Res. 2013 Dec 15;19(24):6777-86. doi: 10.1158/1078-0432.CCR-13-1110. Epub 2013 Oct 24.
4
Phosphoproteomic analysis of anaplastic lymphoma kinase (ALK) downstream signaling pathways identifies signal transducer and activator of transcription 3 as a functional target of activated ALK in neuroblastoma cells.磷酸化蛋白质组学分析间变性淋巴瘤激酶(ALK)下游信号通路发现信号转导子和转录激活子 3 是神经母细胞瘤细胞中激活的 ALK 的功能靶标。
FEBS J. 2013 Nov;280(21):5269-82. doi: 10.1111/febs.12453. Epub 2013 Aug 22.
5
AZD1480: a phase I study of a novel JAK2 inhibitor in solid tumors.AZD1480:一种新型 JAK2 抑制剂在实体瘤中的 I 期研究。
Oncologist. 2013;18(7):819-20. doi: 10.1634/theoncologist.2013-0198. Epub 2013 Jul 11.
6
Inhibition of STAT3 with orally active JAK inhibitor, AZD1480, decreases tumor growth in Neuroblastoma and Pediatric Sarcomas In vitro and In vivo.使用口服活性JAK抑制剂AZD1480抑制STAT3可在体外和体内降低神经母细胞瘤和小儿肉瘤的肿瘤生长。
Oncotarget. 2013 Mar;4(3):433-45. doi: 10.18632/oncotarget.930.
7
Investigational Janus kinase inhibitors.研究性 Janus 激酶抑制剂。
Expert Opin Investig Drugs. 2013 Jun;22(6):687-99. doi: 10.1517/13543784.2013.774373. Epub 2013 Feb 23.
8
U.S. Food and Drug Administration approval: ruxolitinib for the treatment of patients with intermediate and high-risk myelofibrosis.美国食品药品监督管理局批准:芦可替尼治疗中高危骨髓纤维化患者。
Clin Cancer Res. 2012 Jun 15;18(12):3212-7. doi: 10.1158/1078-0432.CCR-12-0653. Epub 2012 Apr 27.
9
Anti-angiogenic activity of a small molecule STAT3 inhibitor LLL12.小分子 STAT3 抑制剂 LLL12 的抗血管生成活性。
PLoS One. 2012;7(4):e35513. doi: 10.1371/journal.pone.0035513. Epub 2012 Apr 17.
10
STAT3 Regulates Proliferation and Immunogenicity of the Ewing Family of Tumors In Vitro.信号转导与转录激活因子3(STAT3)在体外调节尤因家族肿瘤的增殖和免疫原性。
Sarcoma. 2012;2012:987239. doi: 10.1155/2012/987239. Epub 2012 Jan 18.

由儿科临床前测试项目开展的针对Janus激酶1和2抑制剂AZD1480的初始实体瘤测试(1期)。

Initial solid tumor testing (stage 1) of AZD1480, an inhibitor of Janus kinases 1 and 2 by the pediatric preclinical testing program.

作者信息

Houghton Peter J, Kurmasheva Raushan T, Lyalin Dmitry, Maris John M, Kolb E Anders, Gorlick Richard, Reynolds C Patrick, Kang Min H, Keir Stephen T, Wu Jianrong, Smith Malcolm A

机构信息

Nationwide Children's Hospital, Columbus, Ohio.

出版信息

Pediatr Blood Cancer. 2014 Nov;61(11):1972-9. doi: 10.1002/pbc.25175. Epub 2014 Aug 17.

DOI:10.1002/pbc.25175
PMID:25131802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4201390/
Abstract

BACKGROUND

AZD1480 is an ATP competitive inhibitor of Janus kinases 1 and 2 (JAK1, 2) that has been shown to inhibit the growth of solid tumor models. This agent was selected for testing the putative role of JAK/STAT signaling in the standard PPTP solid tumor models.

PROCEDURES

AZD1480 was tested against the PPTP in vitro cell line panel at concentrations from 1.0 nM to 10 μM and against the PPTP in vivo solid tumor xenograft panels at (60 mg/kg once daily (SID) × 5) for three consecutive weeks. Additional studies evaluated 5 to 20 mg/kg BID × 5 with SID dosing at 7-30 mg/kg at weekends for three consecutive weeks.

RESULTS

In vitro the median relative IC50 (rIC50 ) for the PPTP cell lines was 1.5 µM, with a range from 0.3 µM to 5.9 µM. The two cell lines with rIC50 values of 0.3 µM both had ALK activating genomic alterations. AZD1480 demonstrated statistically significant differences (P < 0.05) in EFS distribution compared to control in 89% of the solid tumor xenografts. AZD1480 induced intermediate (EFS T/C > 2) or high-level growth inhibition in 15 of 30 (50%) solid tumor xenografts. Tumor regressions were observed in three of six Wilms tumor models at doses that induced inhibition of Stat3(Y705) phosphorylation.

CONCLUSIONS

AZD1480 demonstrated significant tumor growth inhibition against most PPTP solid tumor xenografts, similar to that observed for antiangiogenic agents tested by the PPTP. Tumor regressing activity was noted for Wilms tumor xenografts.

摘要

背景

AZD1480是一种Janus激酶1和2(JAK1、2)的ATP竞争性抑制剂,已被证明可抑制实体瘤模型的生长。选择该药物在标准PPTP实体瘤模型中测试JAK/STAT信号传导的假定作用。

程序

在体外细胞系组中,以1.0 nM至10 μM的浓度测试AZD1480对PPTP的作用;在体内实体瘤异种移植组中,以60 mg/kg每日一次(SID)×5连续给药三周的方式测试AZD1480对PPTP的作用。另外的研究评估了5至20 mg/kg每日两次×5,并在周末以7 - 30 mg/kg的剂量每日一次给药,连续三周。

结果

在体外,PPTP细胞系的中位相对IC50(rIC50)为1.5 μM,范围为0.3 μM至5.9 μM。rIC50值为0.3 μM的两个细胞系均有ALK激活的基因组改变。与对照组相比,在89%的实体瘤异种移植中,AZD1480在无进展生存期(EFS)分布上显示出统计学显著差异(P < 0.05)。在30个实体瘤异种移植中的15个(50%)中,AZD1480诱导了中度(EFS T/C > 2)或高水平的生长抑制。在六个肾母细胞瘤模型中的三个中,在诱导Stat3(Y705)磷酸化抑制的剂量下观察到肿瘤消退。

结论

AZD1480对大多数PPTP实体瘤异种移植显示出显著的肿瘤生长抑制作用,类似于PPTP测试的抗血管生成药物所观察到的效果。肾母细胞瘤异种移植具有肿瘤消退活性。