Alley M C, Scudiero D A, Monks A, Hursey M L, Czerwinski M J, Fine D L, Abbott B J, Mayo J G, Shoemaker R H, Boyd M R
Program Resources, Inc., National Cancer Institute-Frederick Cancer Research Facility, Maryland 21701.
Cancer Res. 1988 Feb 1;48(3):589-601.
For the past 30 years strategies for the preclinical discovery and development of potential anticancer agents have been based largely upon the testing of agents in mice bearing transplantable leukemias and solid tumors derived from a limited number of murine as well as human sources. The feasibility of implementing an alternate approach, namely combined in vitro/in vivo screening for selective cytotoxicity among panels of human tumor cell lines derived from a broad spectrum of human solid tumors is under investigation. A group of 30 cell lines acquired from a variety of sources and representing 8 lung cancer pathologies as well as 76 cell lines representing 10 other categories of human cancer (carcinomas of colon, breast, kidney, prostate, ovary, head and neck; glioma; leukemia; melanoma; and sarcoma) have exhibited acceptable growth characteristics and suitable colorimetric profiles in a single, standard culture medium. Measurements of in vitro growth in microculture wells by cell-mediated reduction of tetrazolium showed excellent correlation (0.89 less than r2 less than 0.98) with measurements of cellular protein in adherent cell line cultures as well as viable cell count in suspension cell line cultures (0.94 less than r2 less than 0.99). Since the microculture tetrazolium assay provides sensitive and reproducible indices of growth as well as drug sensitivity in individual cell lines over the course of multiple passages and several months' cultivation, it appears suitable for initial-stage in vitro drug screening.
在过去30年里,潜在抗癌药物临床前发现与开发的策略主要基于在携带可移植白血病和实体瘤的小鼠身上测试药物,这些肿瘤来源于有限数量的小鼠以及人类。目前正在研究实施另一种方法的可行性,即在来源于广泛人类实体瘤的一组人类肿瘤细胞系中进行体外/体内联合筛选以检测选择性细胞毒性。从多种来源获取的一组30个细胞系,代表8种肺癌病理类型,以及代表其他10类人类癌症(结肠癌、乳腺癌、肾癌、前列腺癌、卵巢癌、头颈癌;神经胶质瘤;白血病;黑色素瘤;肉瘤)的76个细胞系,在单一标准培养基中显示出可接受的生长特性和合适的比色特征。通过细胞介导的四氮唑还原法在微孔培养板中测量体外生长,与贴壁细胞系培养中的细胞蛋白测量以及悬浮细胞系培养中的活细胞计数显示出极好的相关性(0.89<r²<0.98)(0.94<r²<0.99)。由于微孔培养四氮唑法在多个传代过程和数月培养过程中为单个细胞系的生长以及药物敏感性提供了灵敏且可重复的指标,它似乎适用于体外药物筛选的初始阶段。