Tseng M T, Safa A R
Cancer Detect Prev. 1983;6(3):371-9.
We have developed an in vitro screening test for anticancer agents, using monodispersed tumor cells derived from 7,12-dimethylbenz(a)anthracene (DMBA)-induced mammary tumors in rat. Monolayer cell cultures in multiwell plates are maintained in medium supplemented with hormones and fetal calf serum. Guided by a randomized table, drugs are administered to cultures singly or in combination. Thus far, we have defined dose-response curves for tamoxifen, adriamycin, thiotepa, and methotrexate. Of these agents, adriamycin consistently exhibits a greater cytocidal effect for a given concentration. When these agents are given in combination, a general enhancement of cytotoxicity is observed, although the effects are frequently not additive. Using this procedure, we have examined the drug sensitivity of cells from human tumor biopsies. Data are being compiled for retrospective comparison with the results of treatment for these patients. The procedure described is suitable for analysis of most solid tumors; the evaluation can be completed within 1-2 weeks. Ease of cell maintenance and the brief incubation required suggest that this system may be suitable for general clinical use.
我们已经开发出一种用于抗癌药物的体外筛选试验,该试验使用从7,12-二甲基苯并(a)蒽(DMBA)诱导的大鼠乳腺肿瘤中获取的单分散肿瘤细胞。多孔板中的单层细胞培养物在添加了激素和胎牛血清的培养基中维持生长。根据随机表的指导,将药物单独或联合施用于培养物。到目前为止,我们已经确定了他莫昔芬、阿霉素、噻替派和甲氨蝶呤的剂量反应曲线。在这些药物中,对于给定浓度,阿霉素始终表现出更大的细胞杀伤作用。当这些药物联合使用时,观察到细胞毒性普遍增强,尽管其作用通常并非相加性的。使用该程序,我们已经检测了来自人类肿瘤活检组织的细胞的药物敏感性。正在收集数据以便与这些患者的治疗结果进行回顾性比较。所描述的程序适用于大多数实体瘤的分析;评估可在1-2周内完成。细胞易于维持以及所需的孵育时间较短表明该系统可能适用于一般临床应用。