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特异性识别顺铂损伤DNA的蛋白质:顺铂抗癌活性的线索

Proteins that specifically recognize cisplatin-damaged DNA: a clue to anticancer activity of cisplatin.

作者信息

Zlatanova J, Yaneva J, Leuba S H

机构信息

Department of Biochemistry and Biophysics, Oregon State University, Corvallis 97331-7305, USA.

出版信息

FASEB J. 1998 Jul;12(10):791-9. doi: 10.1096/fasebj.12.10.791.

Abstract

Cisplatin, but not its trans geometric isomer, is a potent anticancer drug whose biological activity is a consequence of the formation of covalent adducts between the platinum compound and certain bases in DNA. Two classes of proteins have recently been identified that bind preferentially to damaged sites: proteins that specifically recognize those sites as a first step in their repair, and those that bind to such sites by virtue of structural similarity between the modified DNA and their own natural binding sites. Both classes of proteins may be involved, perhaps in opposing ways, in the cytotoxic effect of the drug.

摘要

顺铂,而非其反式几何异构体,是一种强效抗癌药物,其生物活性是铂化合物与DNA中某些碱基形成共价加合物的结果。最近已鉴定出两类蛋白质,它们优先结合受损位点:一类蛋白质将这些位点作为修复的第一步进行特异性识别,另一类蛋白质则凭借修饰后的DNA与自身天然结合位点之间的结构相似性而结合到这些位点上。这两类蛋白质可能都以相反的方式参与了药物的细胞毒性作用。

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