Kavanagh T J, Chang C C, Trosko J E
Cancer Res. 1986 Mar;46(3):1359-66.
Although a Chinese hamster V79 cell-based assay for inhibitors of metabolic cooperation is currently available, the development of a human cell-based assay is desirable in order to avoid inappropriate extrapolation from animal cells to human cells. Cells derived from a human teratocarcinoma cell line (designated PA-1), which has a stable pseudodiploid karyotype and excellent in vitro growth properties, were used in a metabolic cooperation assay. The assay was based on the metabolic isolation of hypoxanthine-guanine phosphoribosyltransferase (HGPRT)-deficient variants in the presence of HGPRT-proficient cells and 6-thioguanine. Chemicals which inhibit the transfer of the lethal metabolite of 6-thioguanine from HGPRT-proficient to HGPRT-deficient cells will allow for recovery of the 6-thioguanine-resistant (HGPRT-deficient) cells. Chemicals tested included 12-O-tetradecanoylphorbol-13-acetate and related analogues phorbol-12,13-didecanoate, mezerein, and 4-phorbol-12,13-didecanoate. Concurring with results previously obtained in V79 cells, 12-O-tetradecanoylphorbol-13-acetate and phorbol-12,13-didecanoate strongly inhibited metabolic cooperation, whereas mezerein was moderately inhibitory and 4 alpha-phorbol-12,13-didecanoate was inactive. These cells thus hold promise as a human cell-based assay for inhibitors of metabolic cooperation.
尽管目前已有基于中国仓鼠V79细胞的代谢合作抑制剂检测方法,但为避免从动物细胞不恰当地外推至人类细胞,开发基于人类细胞的检测方法仍很有必要。来自人畸胎瘤细胞系(命名为PA - 1)的细胞具有稳定的假二倍体核型和优良的体外生长特性,被用于代谢合作检测。该检测基于在次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(HGPRT)缺陷型变体存在的情况下,在HGPRT功能正常的细胞和6 - 硫鸟嘌呤存在时进行代谢隔离。抑制6 - 硫鸟嘌呤的致死性代谢产物从HGPRT功能正常的细胞转移至HGPRT缺陷型细胞的化学物质,将使6 - 硫鸟嘌呤抗性(HGPRT缺陷型)细胞得以恢复。所测试的化学物质包括12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯及相关类似物佛波醇 - 12,13 - 十二烷酸酯、美泽瑞因和4 - 佛波醇 - 12,13 - 十二烷酸酯。与先前在V79细胞中获得的结果一致,12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯和佛波醇 - 12,13 - 十二烷酸酯强烈抑制代谢合作,而美泽瑞因具有中等抑制作用,4α - 佛波醇 - 12,13 - 十二烷酸酯无活性。因此,这些细胞有望作为基于人类细胞的代谢合作抑制剂检测方法。