阳离子抗癌药物及其作用方式。

Physiologie (Bucarest) Pub Date : 1989-10-01
G Löber, K Geller, H Hanschmann, L M Popa, R Repanovici, R Iliescu, W Römer, B Janke, V Kleinwächter
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引用次数: 0

摘要

本报告主要针对蒽环类抗生素和1,4-苯醌-鸟酰腙-硫代氨基脲(ambazone)这两类阳离子抗癌药,在膜和膜成分水平上的生物物理和生化作用进行了分析。两种药物与由磷脂酰胆碱组成的多层脂质体作为一个简单的模型膜系统,可以通过稳态和纳秒时间分辨的荧光研究来确保相互作用。通过抑制仙台病毒神经氨酸酶活性、修饰小鼠白血病l1210细胞CAMP磷酸二酯酶活性和减少淋巴细胞成细胞转化,强调了对膜的生化作用。
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Cationic anticancer drugs and their modes of action.

This report focuses on two groups of cationic cancerostatics, anthracycline antibiotics and 1,4-benzoquinone-guanylhydrazone-thiosemicarbazone (ambazone), lining up biophysical and biochemical effects on the level of membranes and membrane constituents. The interaction of both drugs with multilamellar liposomes consisting of phosphatidylcholine used as a simple model membrane system could be ensured by means of steady state and nanosecond time-resolved fluorometric investigations. The biochemical effect on membranes is underlined by the inhibition of the neuraminidase activity of the Sendai virus, modification of the CAMP phosphodiesterase activity of leukemia L 1210 cells of mice and reduction of the lymphocyte blast transformation.

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