Wu P C, Ozols R F, Hatanaka M, Boone C W
J Natl Cancer Inst. 1982 Jan;68(1):115-21.
The effect of 11 anticancer drugs on the ability of Raji lymphoma cells to form colonies in soft agar was determined with the use of both a 1-hour and a continuous drug exposure. Three distinct patterns of drug sensitivities were observed: a) Dactinomycin, adriamycin, bleomycin, mitomycin C, vincristine, and cis-platinum II all produced a dose-dependent reduction in colony formation following a 1-hour exposure, which was further augmented by a continuous exposure to the drugs; b) the antimetabolites (methotrexate, beta-cytosine arabinoside, and 5-fluorouracil) and pentamethylmelamine had no suppressive effects on colony formation with a 1-hour exposure, but they produced marked cytotoxicity with continuous drug exposure; and c) L-phenylalanine mustard had the same degree of colony suppression with both a 1-hour and a continuous drug exposure. Preincubation of Raji cells with an enzyme mixture (DNase + pronase + collagenase) did not alter the degree of colony suppression observed with the anticancer drugs. These results indicate that continuous drug exposure should be compared to a 1-hour drug incubation to determine in vitro drug sensitivities of fresh human tumors in the soft agar clonogenic assay, because the 1-hour drug exposure may not identify certain drugs that are potentially clinically active.
采用1小时和持续药物暴露两种方式,测定了11种抗癌药物对Raji淋巴瘤细胞在软琼脂中形成集落能力的影响。观察到三种不同的药物敏感性模式:a)放线菌素、阿霉素、博来霉素、丝裂霉素C、长春新碱和顺铂II在1小时暴露后均导致集落形成呈剂量依赖性减少,持续暴露于这些药物后这种减少进一步加剧;b)抗代谢物(甲氨蝶呤、β-阿糖胞苷和5-氟尿嘧啶)和六甲蜜胺在1小时暴露时对集落形成无抑制作用,但持续药物暴露时会产生明显的细胞毒性;c)左旋苯丙氨酸氮芥在1小时和持续药物暴露下对集落的抑制程度相同。用酶混合物(脱氧核糖核酸酶+链霉蛋白酶+胶原酶)对Raji细胞进行预孵育,并未改变抗癌药物所观察到的集落抑制程度。这些结果表明,在软琼脂克隆形成试验中,为确定新鲜人肿瘤的体外药物敏感性,应将持续药物暴露与1小时药物孵育进行比较,因为1小时药物暴露可能无法识别某些具有潜在临床活性的药物。