Furukawa T, Kubota T, Watanabe M, Takahara T, Yamaguchi H, Takeuchi T, Kase S, Kodaira S, Ishibiki K, Kitajima M
Department of Surgery, School of Medicine, Keio University, Tokyo, Japan.
Int J Cancer. 1992 May 28;51(3):489-98. doi: 10.1002/ijc.2910510325.
The in vitro sponge-gel-supported three-dimensional histoculture chemosensitivity assay (Hoffman assay) allows the in vivo-like culture of human tumors. In this study, the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H tetrazolium bromide (MTT) end point was applied to the Hoffman assay in an attempt to increase in vitro-in vivo correlation. The chemosensitivities of 16 human tumor lines were determined in vitro by the histoculture assay, and retrospectively correlated to their in vivo chemosensitivity as xenografts in nude mice. The in vitro test was considered to be positive if tumor-cell MTT reduction activity was lowered by more than 50%. The cutoff drug concentrations to determine sensitivity in vitro were determined for mitomycin C, doxorubicin, 5-fluorouracil and cisplatin. Using these cutoff drug concentrations in vitro we found, as a function of time of exposure, a strong correlation between serum drug concentrations found in nude mice given maximum tolerated doses and drug concentrations found in the histoculture media in vitro, thereby establishing a relationship between the amounts of drugs to which tumors were exposed in vivo and in vitro. The overall correlation rate of the efficacy results of the drug-response assay to in vivo chemosensitivities was 89.8%, with 90.0% true-positive and 89.7% true-negative rates, 81.7% sensitivity and 94.6% specificity, thereby indicating potential clinical use for tumor histoculture with the MTT end point.
体外海绵凝胶支持的三维组织培养化学敏感性测定法(霍夫曼测定法)可实现人肿瘤的体内样培养。在本研究中,将3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-2H四唑溴盐(MTT)终点应用于霍夫曼测定法,以提高体外-体内相关性。通过组织培养测定法在体外测定了16种人肿瘤细胞系的化学敏感性,并回顾性地将其与它们作为裸鼠异种移植物的体内化学敏感性相关联。如果肿瘤细胞MTT还原活性降低超过50%,则体外试验被认为是阳性的。确定了丝裂霉素C、阿霉素、5-氟尿嘧啶和顺铂在体外测定敏感性的临界药物浓度。使用这些体外临界药物浓度,我们发现,作为暴露时间的函数,给予最大耐受剂量的裸鼠血清药物浓度与体外组织培养基中发现的药物浓度之间存在很强的相关性,从而建立了肿瘤在体内和体外暴露的药物量之间的关系。药物反应测定的疗效结果与体内化学敏感性的总体相关性为89.8%,真阳性率为90.0%,真阴性率为89.7%,敏感性为81.7%,特异性为94.6%,从而表明具有MTT终点的肿瘤组织培养具有潜在的临床应用价值。