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首页> 外文期刊>British Journal of Cancer >A comparison of adriamycin and mAMSA in vitro: Cell lethality and SCE studies
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A comparison of adriamycin and mAMSA in vitro: Cell lethality and SCE studies

机译:阿霉素和mAMSA的体外比较:细胞致死性和SCE研究

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We have compared the actions of ADM and mAMSA in Chinese hamster V79 cells in vitro, using cell survival and sister-chromatid exchange as end-points. Equimolar concentrations of ADM and mAMSA show similar toxicities to exponentially growing cells, and both drugs are less effective in killing chronically hypoxic and plateau-phase cells. Cytotoxicity to thermotolerant cells (41 degrees C for 16 h previously) shows little difference from that for exponential cells. Pre-treating cells with misonidazole under hypoxic conditions reduces the toxicity of both ADM and mAMSA. In addition, an ADM-resistant Chinese hamster cell line, 77A-177, was cross-resistant to mAMSA. Finally, low equimolar sub-toxic doses of both drugs were found to cause similar increases in the levels of sister-chromatid exchanges in V79 cells. These results reveal no major difference in activity between ADM and mAMSA in vitro.
机译:我们以细胞存活和姐妹染色单体交换为终点,比较了ADM和mAMSA在中国仓鼠V79细胞中的作用。 ADM和mAMSA的等摩尔浓度显示出与成倍增长的细胞相似的毒性,并且两种药物在杀死慢性缺氧和高原期细胞时效果均较差。对耐热细胞的细胞毒性(之前在41摄氏度下持续16 h)与指数细胞的细胞毒性差异不大。在缺氧条件下用米硝唑预处理细胞可降低ADM和mAMSA的毒性。另外,抗ADM的中国仓鼠细胞系77A-177对mAMSA具有交叉抗性。最后,发现两种药物的低等摩尔亚毒性剂量均会导致V79细胞中姐妹染色单体交换的水平出现类似的增加。这些结果表明,ADM和mAMSA在体外的活性没有重大差异。

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