Herrmann Richard, Fayad Walid, Schwarz Stephan, Berndtsson Maria, Linder Stig
Cancer Center Karolinska, Department of Oncology and Pathology, Karolinska Institute and Hospital, Stockholm, Sweden.
J Biomol Screen. 2008 Jan;13(1):1-8. doi: 10.1177/1087057107310442. Epub 2007 Nov 26.
Screening and initial characterization of anticancer drugs are typically performed using monolayer cultures of tumor cells. It is well established that such monolayer cultures do not represent the characteristics of 3-dimensional solid tumors. The multicellular tumor spheroid model is of intermediate complexity between in vivo tumors and in vitro monolayer cultures and would be more suitable for drug screening. The authors describe a procedure in which multicellular spheroids are used to screen for compounds that induce tumor cell apoptosis. Multicellular spheroids were generated in 96-well plates, and apoptosis was determined using the M30-Apoptosense enzyme-linked immunosorbent assay method. A Z' factor of approximately 0.5 was observed for HCT116 colon carcinoma spheroids using staurosporine to induce apoptosis. This procedure is attractive for secondary screening of hits from larger cell-based screens.
抗癌药物的筛选和初步特性鉴定通常使用肿瘤细胞单层培养来进行。众所周知,这种单层培养并不代表三维实体肿瘤的特征。多细胞肿瘤球体模型在体内肿瘤和体外单层培养之间具有中等复杂性,更适合用于药物筛选。作者描述了一种使用多细胞球体筛选诱导肿瘤细胞凋亡化合物的方法。在96孔板中生成多细胞球体,并使用M30-Apoptosense酶联免疫吸附测定法测定细胞凋亡。使用星形孢菌素诱导HCT116结肠癌细胞球体凋亡时,观察到Z'因子约为0.5。该方法对于从更大规模的基于细胞的筛选中筛选出的命中化合物进行二次筛选很有吸引力。