Kwok T T, Twentyman P R
Br J Cancer. 1987 Apr;55(4):367-74. doi: 10.1038/bjc.1987.74.
A technique using 'tritiated thymidine suicide' has been established as a means of studying the response to cytotoxic drugs of cells at different depths within multicellular tumour spheroids. Because of the characteristic spatial arrangement of cycling cells (mostly in the outer regions) and non-cycling cells (mostly at the inner regions) of spheroids, cells surviving after long term (24 h) exposure of spheroids to high doses of 3HTdR will be those located furthest from the surface. By comparing the drug response of cells from 3HTdR pre-treated and untreated spheroids, the individual response of total cells, cells near to the surface and cells lying deeper within the viable rim of spheroids can therefore be deduced. In this study, large spheroids of about 800 micron in diameter of a mouse mammary cell line, EMT6/Ca/VJAC, and of a human small cell lung cancer cell line, POC, have been used. Using clonogenic assay, the response of these two cell types to adriamycin (ADM), nitrogen mustard (HN2), CCNU and vincristine (VCR) (POC only) were measured. The preliminary part of this study has confirmed that the cells killed are those which incorporate 3HTdR during the DNA synthesis period; the cells killed are mainly located in the outer regions of spheroids i.e. surviving cells are mostly located in the inner part of the viable rim and 3HTdR pretreatment does not sensitise surviving cells to subsequent cytotoxic drug treatment. Results from large EMT6 spheroids agree with our previous findings (obtained using a selective disaggregation method) that cells in the outer regions of spheroids are more sensitive to ADM and HN2 than cells in the inner regions whilst the opposite is true for CCNU. For POC spheroids, cells in the outer region of spheroids are more sensitive to ADM and VCR than cells in the inner region whilst a reverse trend is seen for the response to CCNU. The response to HN2 is similar at all depths. Amongst the factors governing the response of cells in spheroids to cytotoxic drugs, the responses to ADM and VCR are thought to be largely dictated by cell cycle distribution and limited drug penetrability, whilst for HN2 the response may be determined by the factor of cell cycle distribution. For CCNU, we believe that the cellular response is largely dependent upon microenvironmental factors prevailing within spheroids.
一种利用“氚标记胸腺嘧啶核苷自杀法”的技术已被确立,作为研究多细胞肿瘤球体不同深度细胞对细胞毒性药物反应的一种手段。由于球体中循环细胞(大多位于外部区域)和非循环细胞(大多位于内部区域)具有特征性的空间排列,球体在高剂量3HTdR下长期(24小时)暴露后存活的细胞将是那些距离表面最远的细胞。通过比较经3HTdR预处理和未经处理的球体中细胞的药物反应,因此可以推断出总细胞、靠近表面的细胞以及位于球体存活边缘较深处的细胞的个体反应。在本研究中,使用了小鼠乳腺细胞系EMT6/Ca/VJAC和人小细胞肺癌细胞系POC的直径约800微米的大球体。采用克隆形成试验,测量了这两种细胞类型对阿霉素(ADM)、氮芥(HN2)、环己亚硝脲(CCNU)和长春新碱(VCR)(仅针对POC)的反应。本研究的初步部分证实,被杀死的细胞是那些在DNA合成期掺入3HTdR的细胞;被杀死的细胞主要位于球体的外部区域,即存活细胞大多位于存活边缘的内部,并且3HTdR预处理不会使存活细胞对随后的细胞毒性药物治疗敏感。来自大型EMT6球体的结果与我们之前的发现(使用选择性解离方法获得)一致,即球体外部区域的细胞比内部区域的细胞对ADM和HN2更敏感,而对于CCNU则相反。对于POC球体,球体外部区域的细胞比内部区域的细胞对ADM和VCR更敏感,而对CCNU的反应则呈现相反趋势。在所有深度对HN2的反应相似。在决定球体中细胞对细胞毒性药物反应的因素中,对ADM和VCR的反应被认为很大程度上由细胞周期分布和有限的药物渗透性决定,而对于HN2,反应可能由细胞周期分布因素决定。对于CCNU,我们认为细胞反应很大程度上取决于球体中普遍存在的微环境因素。