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儿科临床前测试项目对VNP40101M(氯雷他嗪)进行的初步测试。

Initial testing of VNP40101M (Cloretazine) by the pediatric preclinical testing program.

作者信息

Keir Stephen T, Morton Christopher L, Billups Catherine, Smith Malcolm A, Houghton Peter J, Gururangan Sridharan

机构信息

Preston Robert Tisch Brain Tumor Center, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Pediatr Blood Cancer. 2008 Sep;51(3):439-41. doi: 10.1002/pbc.21620.

Abstract

VNP40101M is a novel alkylating agent that yields two reactive compounds (a chloroethylating species and methylisocyanate) and has demonstrated activity against a wide spectrum of tumor xenografts. VNP40101M was tested against an in vivo panel of five pediatric brain tumor xenografts at a dose of 18 mg/kg/day administered for 5 days. O-6-methylguanine-DNA methyltransferase (MGMT) levels of xenografts were assessed by Western blot analysis. Only one xenograft (GBM2), which lacked detectable MGMT expression, demonstrated an objective response to VNP40101M. VNP4010M antitumor activity was observed only in the absence of MGMT expression, with resistance to VNP4010M seen even with low MGMT expression.

摘要

VNP40101M是一种新型烷化剂,可产生两种活性化合物(一种氯乙基化物质和甲基异氰酸酯),并已证明对多种肿瘤异种移植模型具有活性。以18mg/kg/天的剂量对一组五种小儿脑肿瘤异种移植模型进行了VNP40101M的体内试验,持续给药5天。通过蛋白质印迹分析评估异种移植模型的O-6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)水平。只有一个缺乏可检测到的MGMT表达的异种移植模型(GBM2)对VNP40101M表现出客观反应。仅在没有MGMT表达的情况下观察到VNP4010M的抗肿瘤活性,即使MGMT表达水平较低也会出现对VNP4010M的耐药性。

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