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
Nationwide Children's Hospital, Columbus, Ohio.
Pediatr Blood Cancer. 2014 Nov;61(11):1972-9. doi: 10.1002/pbc.25175. Epub 2014 Aug 17.
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.
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.
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.
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.
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。
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。
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。
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。