Rasey J S, Nelson N J
Br J Cancer Suppl. 1980 Apr;4:217-21.
EMT-6/UW tumours were treated in vivo with X-rays, cyclophosphamide, or bleomycin. Cell survival was assayed in vitro following tumour disaggregation with trypsin or an enzyme cocktail (EC) consisting of pronase, collagenase and DNase which gives a 10-20 x higher cell yield. Surviving fraction was lower after cyclophosphamide treatment for cells isolated with EC than for cells prepared with trypsin. The opposite result was obtained with bleomycin; trypsin-isolated cells appeared more sensitive. In attempting to determine the basis for this discrepancy, it was found that both dissociation methods isolate a non-representative cell sample with fewer cells in DNA synthesis (12-13%) than in the original tumour (approximately 22%). The specific nature of the interaction between the injury caused by drug and enzyme remains to be elucidated.
将 EMT-6/UW 肿瘤在体内用 X 射线、环磷酰胺或博来霉素进行治疗。肿瘤用胰蛋白酶或由链霉蛋白酶、胶原酶和脱氧核糖核酸酶组成的酶混合物(EC)进行解离后,在体外测定细胞存活率,酶混合物解离后的细胞产量比胰蛋白酶高 10 - 20 倍。用 EC 分离的细胞经环磷酰胺处理后的存活分数低于用胰蛋白酶制备的细胞。博来霉素处理则得到相反的结果;用胰蛋白酶分离的细胞似乎更敏感。在试图确定这种差异的原因时,发现两种解离方法分离出的细胞样本都不具有代表性,处于 DNA 合成期的细胞数量(12 - 13%)比原始肿瘤中的细胞数量(约 22%)少。药物和酶所造成损伤之间相互作用的具体性质仍有待阐明。