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阿霉素对转录的抑制作用是由拓扑异构酶II介导的DNA负超螺旋性丧失的结果。

Inhibition of transcription by adriamycin is a consequence of the loss of negative superhelicity in DNA mediated by topoisomerase II.

作者信息

Tarr M, van Helden P D

机构信息

Department of Medical Biochemistry, University of Stellenbosch, Tygerberg, South Africa.

出版信息

Mol Cell Biochem. 1990 Mar 27;93(2):141-6. doi: 10.1007/BF00226185.

Abstract

Adriamycin is commonly used as a chemotherapeutic agent and is known to intercalate into the major groove of DNA and inhibit DNA and RNA synthesis. Results presented in this communication suggest that adriamycin affects topoisomerase cleavage of DNA. The resultant change in negative superhelicity (decrease) is responsible for the decrease in transcription. This process is not dependent on the continued presence of adriamycin. The reaction between topoisomerases, DNA and adriamycin is dose-dependent. The results help to explain the relatively enhanced cytotoxicity of this drug to tumor cells.

摘要

阿霉素通常用作化疗药物,已知它可嵌入DNA的大沟并抑制DNA和RNA合成。本通讯中给出的结果表明,阿霉素会影响DNA拓扑异构酶的切割。负超螺旋度的最终变化(降低)导致转录减少。这个过程不依赖于阿霉素的持续存在。拓扑异构酶、DNA和阿霉素之间的反应是剂量依赖性的。这些结果有助于解释这种药物对肿瘤细胞相对增强的细胞毒性。

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