Gábelová A, Slamenová D
Cancer Research Institute, Slovak Academy of Sciences, Bratislava.
Neoplasma. 1991;38(1):85-91.
Many chemicals which promote tumorigenesis in vivo have been observed to inhibit metabolic cooperation between 6-thioguanine-resistant (6TGr) and sensitive (6TGs) Chinese hamster lung V79 cells. The apparent correlation between inhibition of metabolic cooperation in V79 cells in vitro and promotion of oncogenesis in vivo has led to the suggested utilization of the assay as a screen for tumor promoters. Several parameters concerning the V79 metabolic cooperation assay were investigated for an improved understanding of the usefulness and limitations of the assay in our laboratory conditions. We have found that the recovery of 6TGr cells were dependent upon the number of 6TGs cells plated, upon the generation time, passage number, and upon the co-cultivation period until the addition of selective agent. The ability of this assay to detect tumor promoters has been determined by the known tumor promoter phorbol ester TPA.
许多在体内可促进肿瘤发生的化学物质,已被观察到能抑制6-硫代鸟嘌呤抗性(6TGr)和敏感(6TGs)的中国仓鼠肺V79细胞之间的代谢协同作用。体外V79细胞中代谢协同作用的抑制与体内肿瘤发生促进之间的明显相关性,已促使人们建议将该检测方法用作肿瘤促进剂的筛选方法。为了更好地理解该检测方法在我们实验室条件下的有用性和局限性,我们研究了与V79代谢协同检测相关的几个参数。我们发现,6TGr细胞的恢复取决于接种的6TGs细胞数量、代时、传代次数以及添加选择剂之前的共培养时间。该检测方法检测肿瘤促进剂的能力已通过已知的肿瘤促进剂佛波酯TPA得以确定。