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阿霉素与氨苯吖啶的体外比较:细胞致死率及姐妹染色单体交换研究

A comparison of adriamycin and mAMSA in vitro: cell lethality and SCE studies.

作者信息

West C, Stratford I J, Barrass N, Smith E

出版信息

Br J Cancer. 1981 Dec;44(6):798-809. doi: 10.1038/bjc.1981.278.

Abstract

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.

摘要

我们使用细胞存活率和姐妹染色单体交换作为终点指标,在体外比较了阿霉素(ADM)和胺苯吖啶(mAMSA)对中国仓鼠V79细胞的作用。阿霉素和胺苯吖啶的等摩尔浓度对指数生长期细胞显示出相似的毒性,并且两种药物在杀死慢性缺氧细胞和平台期细胞方面效果较差。对热耐受细胞(先前在41℃下处理16小时)的细胞毒性与指数生长期细胞相比几乎没有差异。在缺氧条件下用米索硝唑预处理细胞可降低阿霉素和胺苯吖啶的毒性。此外,一种耐阿霉素的中国仓鼠细胞系77A - 177对胺苯吖啶也具有交叉抗性。最后,发现两种药物的低等摩尔亚毒性剂量均可使V79细胞中的姐妹染色单体交换水平产生相似的增加。这些结果表明,阿霉素和胺苯吖啶在体外的活性没有重大差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7518/2010861/1eafe5fa10cb/brjcancer00447-0034-a.jpg

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