Menconi E, Lepri E, Bonmassar E, Frati L, Barzi A
Int J Tissue React. 1986;8(6):485-92.
The present study was aimed at defining the standard conditions for predictive chemosensitivity testing of human leukaemias. The in vitro cytotoxic potential of 11 anticancer drugs against L1210 murine leukaemia was comparatively determined 3 and 48 h after in vitro exposure of leukaemia cells to these agents. In preliminary testing, drug-induced damage was estimated in terms of percent inhibition of: tumour cell proliferation, by microscopic determination of viable cell numbers; and DNA synthesis, by measuring the extent of incorporation of the labelled nucleoside 125IUdR. Since the two tests appeared to yield comparable results, all subsequent experiments on the various murine tumours were performed using the radiolabel incorporation technique. The results obtained pointed out that this metabolic assay performed 48 hours after drug exposure appears to be capable of predicting both "spontaneous" and "induced" in vivo resistance of murine leukaemias.
本研究旨在确定人类白血病预测性化学敏感性测试的标准条件。在白血病细胞体外暴露于11种抗癌药物3小时和48小时后,比较测定了这些药物对L1210小鼠白血病的体外细胞毒性潜力。在初步测试中,通过显微镜下测定活细胞数量来估计药物诱导的损伤,以肿瘤细胞增殖抑制百分比表示;通过测量标记核苷125IUdR的掺入程度来估计DNA合成。由于这两种测试似乎产生了可比的结果,因此随后对各种小鼠肿瘤进行的所有实验均使用放射性标记掺入技术。所获得的结果指出,在药物暴露48小时后进行的这种代谢测定似乎能够预测小鼠白血病的“自发”和“诱导”体内抗性。