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通过人肿瘤克隆系统测定阿霉素、米托蒽醌和比生群的比较细胞毒性。

Comparative cytotoxicity of adriamycin, mitoxantrone and bisantrene as measured by a human tumor cloning system.

作者信息

Cowan J D, Von Hoff D D, Clark G M

出版信息

Invest New Drugs. 1983;1(2):139-44. doi: 10.1007/BF00172072.

Abstract

A human tumor cloning system was used to assess the cytotoxicity of adriamycin, mitoxantrone and bisantrene at concentrations that are equitoxic in man. There were 989 specimens evaluable for drug sensitivity analysis. Overall, adriamycin showed in vitro cytotoxicity (greater than or equal to 50% decrease in tumor colony forming units) 14% of the time; mitoxantrone, 21% of the time; and bisantrene, 31% of the time. Three hundred ninety-nine of these evaluable specimens were simultaneously tested against more than one of the agents, providing 631 two-way drug comparisons. For these comparisons, there was lack of co-resistance 27-34% of the time, with mitoxantrone being more active than adriamycin (p less than .05) and bisantrene being more active than adriamycin (p less than .01) or mitoxantrone (p less than .01). These data suggest that comparative and sequential clinical use of these agents should be investigated.

摘要

使用一种人类肿瘤克隆系统来评估阿霉素、米托蒽醌和比生群在对人体具有同等毒性的浓度下的细胞毒性。有989个标本可用于药物敏感性分析。总体而言,阿霉素在14%的时间里表现出体外细胞毒性(肿瘤集落形成单位减少大于或等于50%);米托蒽醌为21%的时间;比生群为31%的时间。这些可评估标本中的399个同时针对不止一种药物进行了测试,提供了631次双向药物比较。对于这些比较,27% - 34%的时间缺乏共同耐药性,米托蒽醌比阿霉素更具活性(p小于0.05),比生群比阿霉素(p小于0.01)或米托蒽醌(p小于0.01)更具活性。这些数据表明,应该对这些药物的比较性和序贯性临床应用进行研究。

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