Children's Hospital of Philadelphia, Philadelphia, PA 19104-4318, USA.
Pediatr Blood Cancer. 2012 Oct;59(4):749-52. doi: 10.1002/pbc.23364. Epub 2011 Nov 2.
The PIM kinase inhibitor, SGI-1776, was tested against the PPTP in vitro (1.0 nM-10 µM) and in vivo panels (148 mg/kg daily × 5 days for 3 weeks). SGI-1776 exhibited cytotoxic activity in vitro with a median relative IC(50) of 3.1 µM. SGI-1776 induced significant differences in EFS distribution in vivo in 9 of 31 solid tumor xenografts and in 1 of 8 of the evaluable ALL xenografts. SGI-1776 induced tumor growth inhibition meeting criteria for intermediate EFS T/C activity in 1 of 39 evaluable models. In contrast, SGI-1776 induced complete responses of subcutaneous MV4;11 (B myeloid leukemia).
PIM 激酶抑制剂 SGI-1776 在体外(1.0 nM-10 μM)和体内(148 mg/kg 每日×5 天,共 3 周)对 PPTP 进行了测试。SGI-1776 在体外具有细胞毒性活性,中位相对 IC50 为 3.1 μM。SGI-1776 在 31 种实体瘤异种移植中的 9 种和 8 种可评估 ALL 异种移植中的 1 种体内诱导 EFS 分布的显著差异。SGI-1776 在 39 种可评估模型中的 1 种诱导符合中间 EFS T/C 活性标准的肿瘤生长抑制。相比之下,SGI-1776 诱导皮下 MV4;11(B 髓性白血病)完全缓解。