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Smac mimetics: implications for enhancement of targeted therapies in leukemia.Smac 模拟物:在白血病靶向治疗中的增强作用。
Leukemia. 2010 Dec;24(12):2100-9. doi: 10.1038/leu.2010.212. Epub 2010 Sep 16.
2
IAPs: from caspase inhibitors to modulators of NF-kappaB, inflammation and cancer.IAPs:从细胞胱冬酶抑制剂到 NF-κB、炎症和癌症的调节剂。
Nat Rev Cancer. 2010 Aug;10(8):561-74. doi: 10.1038/nrc2889.
3
Both cIAP1 and cIAP2 regulate TNFalpha-mediated NF-kappaB activation.细胞凋亡抑制蛋白1(cIAP1)和细胞凋亡抑制蛋白2(cIAP2)均调节肿瘤坏死因子α(TNFα)介导的核因子κB(NF-κB)激活。
Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):11778-83. doi: 10.1073/pnas.0711122105. Epub 2008 Aug 12.
4
Molecular characterization of the pediatric preclinical testing panel.儿科临床前测试小组的分子特征分析。
Clin Cancer Res. 2008 Jul 15;14(14):4572-83. doi: 10.1158/1078-0432.CCR-07-5090.
5
c-IAP1 and c-IAP2 are critical mediators of tumor necrosis factor alpha (TNFalpha)-induced NF-kappaB activation.细胞凋亡抑制蛋白1(c-IAP1)和细胞凋亡抑制蛋白2(c-IAP2)是肿瘤坏死因子α(TNFα)诱导的核因子κB(NF-κB)激活的关键介质。
J Biol Chem. 2008 Sep 5;283(36):24295-9. doi: 10.1074/jbc.C800128200. Epub 2008 Jul 11.
6
cIAP1 and cIAP2 facilitate cancer cell survival by functioning as E3 ligases that promote RIP1 ubiquitination.cIAP1和cIAP2作为促进RIP1泛素化的E3连接酶发挥作用,从而促进癌细胞存活。
Mol Cell. 2008 Jun 20;30(6):689-700. doi: 10.1016/j.molcel.2008.05.014.
7
Initial testing of VNP40101M (Cloretazine) by the pediatric preclinical testing program.儿科临床前测试项目对VNP40101M(氯雷他嗪)进行的初步测试。
Pediatr Blood Cancer. 2008 Sep;51(3):439-41. doi: 10.1002/pbc.21620.
8
A Smac mimetic rescue screen reveals roles for inhibitor of apoptosis proteins in tumor necrosis factor-alpha signaling.一项Smac模拟物拯救筛选揭示了凋亡抑制蛋白在肿瘤坏死因子-α信号传导中的作用。
Cancer Res. 2007 Dec 15;67(24):11493-8. doi: 10.1158/0008-5472.CAN-07-5173.
9
Autocrine TNFalpha signaling renders human cancer cells susceptible to Smac-mimetic-induced apoptosis.自分泌肿瘤坏死因子α信号使人类癌细胞对Smac模拟物诱导的凋亡敏感。
Cancer Cell. 2007 Nov;12(5):445-56. doi: 10.1016/j.ccr.2007.08.029.
10
Initial testing (stage 1) of the proteasome inhibitor bortezomib by the pediatric preclinical testing program.儿科临床前测试项目对蛋白酶体抑制剂硼替佐米进行的初始测试(第1阶段)。
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由儿科临床前测试计划进行的 SMAC 模拟物 LCL161 的初步测试(第 1 阶段)。

Initial testing (stage 1) of LCL161, a SMAC mimetic, by the Pediatric Preclinical Testing Program.

机构信息

Nationwide Children's Hospital, Columbus, Ohio 43205, USA.

出版信息

Pediatr Blood Cancer. 2012 Apr;58(4):636-9. doi: 10.1002/pbc.23167. Epub 2011 Jun 16.

DOI:10.1002/pbc.23167
PMID:21681929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3253328/
Abstract

LCL161, a SMAC mimetic, was tested against the PPTP in vitro panel (1.0 nM to 10.0 µM) and the PPTP in vivo panels (30 or 75 mg/kg [solid tumors] or 100 mg/kg [ALL]) administered orally twice in a week. LCL161 showed a median relative IC(50) value of >10 µM, being more potent against several leukemia and lymphoma lines. In vivo LCL161 induced significant differences in EFS distribution in approximately one-third of solid tumor xenografts (osteosarcoma and glioblastoma), but not in ALL xenografts. No objective tumor responses were observed. In vivo LCL161 demonstrated limited single agent activity against the pediatric preclinical models studied.

摘要

LCL161 是一种 SMAC 模拟物,在体外(1.0 nM 至 10.0 μM)和体内(30 或 75 mg/kg [实体瘤]或 100 mg/kg [ALL])PPTP 检测面板中进行了测试,通过口服每周两次。LCL161 显示出中值相对 IC(50)值 >10 μM,对几种白血病和淋巴瘤系更有效。在体内,LCL161 在大约三分之一的实体瘤异种移植瘤(骨肉瘤和神经胶质瘤)中诱导 EFS 分布的显著差异,但在 ALL 异种移植瘤中没有。没有观察到客观的肿瘤反应。在体内,LCL161 对所研究的儿科临床前模型显示出有限的单一药物活性。