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[恶性肿瘤对细胞抑制剂的体外和体内敏感性试验/对小鼠肉瘤180的研究(作者译)]

[Sensitivity tests of malignant tumours against cytostatic agents in vitro and in vivo/studies on the mouse sarcoma 180 (author's transl)].

作者信息

Volm M, Kaufmann M, Mattern J, Wayss K

出版信息

Arzneimittelforschung. 1975 Jul;25(7):1042-8.

PMID:52364
Abstract

The effects of ten different substances on the mouse sarcoma 180 have been compared using in vivo and in vitro test systems. The size of the tumours was taken as a measure of the success of the therapy in animal experiments. The in vitro effects were estimated by measuring the incorporation of radioactively labelled uridine in tumour cell suspensions from solid tumours, in ascites tumours and in tissue culture. Similar results were obtained using all three in vitro test systems. Four substances (daunomycin, fluoruracil, actinomycin D, adriamycin) exhibited activity both in vivo and in vitro, whereas five substances (cytosinarabinoside, methotrexate, ibenzmethyzin, triaziquone, bleomycin) showed no activity in any of the test systems used. With podophyllic acid ethyl hydrazide, however, no correlation between in vivo and in vitro effects was observed. Studies on the influence of the cytostatic agents on the rate of transport of uridine into the cells showed that podophyllic acid ethyl hydrazide strongly reduced the permeability of the cells to radioactive uridine.

摘要

已使用体内和体外测试系统比较了十种不同物质对小鼠肉瘤180的作用。在动物实验中,肿瘤大小被用作衡量治疗效果的指标。通过测量放射性标记的尿苷在实体瘤、腹水瘤和组织培养的肿瘤细胞悬液中的掺入量来评估体外效应。使用所有三种体外测试系统均获得了相似的结果。四种物质(柔红霉素、氟尿嘧啶、放线菌素D、阿霉素)在体内和体外均表现出活性,而五种物质(阿糖胞苷、甲氨蝶呤、异丁嗪、三嗪醌、博来霉素)在所用的任何测试系统中均无活性。然而,对于鬼臼酸乙酯肼,未观察到体内和体外效应之间的相关性。关于细胞抑制剂对尿苷进入细胞速率的影响的研究表明,鬼臼酸乙酯肼强烈降低了细胞对放射性尿苷的通透性。

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