1,3-双-(2-氯乙基)-1-亚硝基脲和顺铂诱导的脑胶质瘤细胞总基因组DNA链间交联的形成和修复。

Cancer biochemistry biophysics Pub Date : 1995-01-01
F Ali-Osman, A Rairkar, P Young
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引用次数: 0

摘要

研究了BCNU和顺式ddp诱导的总基因组DNA链间交联(ISCs)在6种人恶性胶质瘤细胞中形成和修复的动力学及其与耐药程度的关系。暴露于50微米BCNU或25微米顺式ddp 2小时后,DNA ISCs迅速形成(峰值6-12小时),在等摩尔的基础上,顺式ddp的交联水平高于BCNU。顺式ddp诱导的交联具有双相修复的特点,修复速率显著高于BCNU诱导的交联。总体而言,低交联指数和高交联修复率与cis-DDP和BCNU抗性相关。这些数据最终证明了人类胶质瘤细胞修复顺式ddp和BCNU诱导的DNA ISCs的能力,并且DNA交联修复是这些肿瘤对这两种药物产生耐药性的重要因素。
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Formation and repair of 1,3-bis-(2-chloroethyl)-1-nitrosourea and cisplatin induced total genomic DNA interstrand crosslinks in human glioma cells.

The kinetics of formation and repair of total genomic DNA interstrand crosslinks (ISCs) induced by BCNU and cis-DDP were studied in cells of 6 human malignant gliomas and related with their degree of drug resistance. DNA ISCs were formed rapidly (peak 6-12 h) following a 2 h exposure to 50 microM BCNU or 25 uM cis-DDP, and on an equimolar basis higher levels of crosslinking were observed with cis-DDP than with BCNU. Repair of cis-DDP induced crosslinks was characteristically bi-phasic and the rate was significantly higher than that for BCNU induced crosslinks. Overall, a low crosslink index and a high crosslink repair rate correlated with cis-DDP and BCNU resistance. The data demonstrate, conclusively, the ability of human glioma cells to repair cis-DDP and, for the first time, BCNU induced DNA ISCs and that DNA crosslink repair is a significant contributing factor to the resistance of these tumors to the two agents.

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