Tomlinson F H, Lihou M G, Smith P J
Queensland Institute of Medical Research, Brisbane, Australia.
Br J Cancer. 1991 Dec;64(6):1051-9. doi: 10.1038/bjc.1991.464.
Surgical specimens from 15 medulloblastoma patients were used to establish early passage cultures. In vitro sensitivity to a battery of cytotoxic agents, including some in current medulloblastoma treatment protocols, was measured. Drug sensitivity was assessed at clinically relevant drug concentrations using the 3H-thymidine uptake method. Tumours were predicted to be sensitive if greater than 37% were killed by exposure to drugs at clinically achievable levels. A poor response to vincristine (Vcr), cis-platin (CDDP), hydroxyurea (HU) or diaziquone (AZQ) (no responders), and cytosine arabinoside (AraC) (1/12), was seen. Nine of ten tumours tested were sensitive to mafosfamide (Mfs); seven out of 12 were sensitive to carmustine (BCNU), 12 of 13 to teniposide (VM-26) and seven of 13 to etoposide (VP16-213). VM-26 was the best of the agents tested with most tumours responding to very low concentrations of drug, suggesting that the role of epipodophyllotoxins in treatment of brain tumours be further investigated. Despite the marked sensitivity of the medulloblastomas to the epipodophyllotoxins, three early passage cultures were much more resistant to these drugs than the average for the group. The basis of this resistance was investigated. Deficient cellular uptake of drug was excluded as a cause of resistance. One resistant early passage culture displayed low cellular activity of topoisomerase II and decreased levels of drug induced enzyme-DNA strand break activity. This was not the case for the other resistant early passage cultures: the basis of resistance in these cells does not appear to be due to any previously reported mechanism.
取自15例髓母细胞瘤患者的手术标本用于建立早期传代培养。测定了对一系列细胞毒性药物的体外敏感性,其中包括一些目前髓母细胞瘤治疗方案中使用的药物。使用³H-胸腺嘧啶核苷摄取法在临床相关药物浓度下评估药物敏感性。如果在临床可达到的水平下,超过37%的肿瘤细胞因接触药物而死亡,则预测该肿瘤对药物敏感。观察到对长春新碱(Vcr)、顺铂(CDDP)、羟基脲(HU)或重氮醌(AZQ)(无反应者)以及阿糖胞苷(AraC)(1/12)反应不佳。所测试的10个肿瘤中有9个对马法兰(Mfs)敏感;12个中有7个对卡莫司汀(BCNU)敏感,13个中有12个对替尼泊苷(VM-26)敏感,13个中有7个对依托泊苷(VP16-213)敏感。VM-26是所测试药物中效果最好的,大多数肿瘤对极低浓度的药物有反应,这表明应进一步研究表鬼臼毒素在脑肿瘤治疗中的作用。尽管髓母细胞瘤对表鬼臼毒素有明显的敏感性,但有3个早期传代培养物对这些药物的耐药性比该组平均水平高得多。对这种耐药性的基础进行了研究。药物细胞摄取不足被排除为耐药原因。一个耐药的早期传代培养物显示拓扑异构酶II的细胞活性低,药物诱导的酶-DNA链断裂活性水平降低。其他耐药的早期传代培养物并非如此:这些细胞的耐药基础似乎不是由于任何先前报道的机制。