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O6-苄基鸟嘌呤对间变性胶质瘤中O6-烷基鸟嘌呤-DNA烷基转移酶的抑制作用

O6-benzylguanine suppression of O6-alkylguanine-DNA alkyltransferase in anaplastic gliomas.

作者信息

Schold S Clifford, Kokkinakis Demetrius M, Chang Susan M, Berger Mitchel S, Hess Kenneth R, Schiff David, Robins H Ian, Mehta Minesh P, Fink Karen L, Davis R L, Prados Michael D

机构信息

University of Pittsburgh Cancer Institute, Pittsburgh, PA 15232, USA.

出版信息

Neuro Oncol. 2004 Jan;6(1):28-32. doi: 10.1215/s115285170300019x.

Abstract

The purpose of the study was to determine the dose of O(6)-benzylguanine (BG) that would suppress O(6)-alkylguanine-DNA alkyltransferase (AGT) activity to undetectable levels in > 90% of anaplastic gliomas, as measured 6 h after a 1-h BG infusion. Subjects who were scheduled for surgical resection of a known or presumed anaplastic glioma received a 1-h infusion of BG. Tumor tissue was surgically removed approximately 6 h after the end of the infusion and was analyzed for AGT activity. The BG dose was escalated until at least 11 of 14 subjects had no detectable AGT activity. An additional cohort of patients received the identified effective dose of BG approximately 18 h before tumor resection in order to compare our results with an earlier study using the longer time interval. In the 79 subjects who were enrolled, there was no significant toxicity that was attributed to the BG. A dose-response relationship was determined between the BG dose and the percentage of subjects with undetectable AGT. A dose of 120 mg/m(2) suppressed AGT to less than detectable levels in 17 of 18 patients when the drug-resection interval was 6 h. With an 18-h interval, only 5 of 11 subjects had undetectable AGT at the 120-mg/m(2) dose. We conclude that a BG dose of 120 mg/m(2) given 6 h before an alkylating drug would be effective in suppressing AGT and possibly potentiating the cytotoxic effects of the drug.

摘要

本研究的目的是确定O(6)-苄基鸟嘌呤(BG)的剂量,该剂量能在1小时BG输注后6小时测量时,将90%以上的间变性胶质瘤中的O(6)-烷基鸟嘌呤-DNA烷基转移酶(AGT)活性抑制到无法检测的水平。计划对已知或疑似间变性胶质瘤进行手术切除的受试者接受1小时的BG输注。在输注结束后约6小时手术切除肿瘤组织,并分析其AGT活性。逐步增加BG剂量,直到14名受试者中至少11名的AGT活性无法检测到。另一组患者在肿瘤切除前约18小时接受确定的有效剂量的BG,以便将我们的结果与使用较长时间间隔的早期研究进行比较。在纳入的79名受试者中,没有明显的毒性可归因于BG。确定了BG剂量与AGT无法检测的受试者百分比之间的剂量反应关系。当药物-切除间隔为6小时时,120mg/m²的剂量可使18名患者中的17名的AGT抑制到低于可检测水平。间隔18小时时,在120mg/m²剂量下,11名受试者中只有5名的AGT无法检测到。我们得出结论,在给予烷化剂药物前6小时给予120mg/m²的BG剂量可有效抑制AGT,并可能增强药物的细胞毒性作用。

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