Johnson R K, Chitnis M P, Embrey W M, Gregory E B
Cancer Treat Rep. 1978 Oct;62(10):1535-47.
A subline of P388 leukemia resistant to adriamycin (P388/ADR) was developed by exposure to the drug in vivo. Resistance to adriamycin proved to be a stable characteristic of P388/ADR. There was no significant inhibition of nucleic acid synthesis in P388/ADR cells in vivo following a dose of 10 mg/kg of adriamycin in contrast to a prolonged and complete inhibition, particularly of DNA synthesis, observed in parental sensitive P388 leukemia cells. P388/ADR proved to be completely cross-resistant to a spectrum of anthracycline derivatives. Cross-resistance was observed to nonanthracycline DNA intercalating agents (with the exception of anthramycin), to agents which interfere with mitotic spindle function, and to antineoplastic inhibitors of protein biosynthesis (with the exception of bruceantin). P388/ADR was sensitive to antimetabolites and alkylating agents. Cross-resistance was also observed to several agents (ICRF-159, a terephthalanilide, taxol, lymphosarcin, bouvardin, and a crude extract of Ervatamia hyneana) whose mechanisms of action have not yet been clearly defined. This observation has proved useful in providing a lead for determination of mechanism of action of some of these drugs. The pattern of cross-resistance of a subline of P388 leukemia resistant to daunorubicin, though not studied extensively, appears to be similar to that of P388/ADR.
通过在体内接触阿霉素培育出了一株对阿霉素耐药的P388白血病亚系(P388/ADR)。对阿霉素的耐药性被证明是P388/ADR的一个稳定特征。与在亲代敏感的P388白血病细胞中观察到的长时间且完全的抑制作用,尤其是对DNA合成的抑制作用相比,给予10mg/kg阿霉素剂量后,P388/ADR细胞在体内的核酸合成没有受到显著抑制。P388/ADR被证明对一系列蒽环类衍生物完全交叉耐药。观察到对非蒽环类DNA嵌入剂(除氨茴霉素外)、干扰有丝分裂纺锤体功能的药物以及蛋白质生物合成的抗肿瘤抑制剂(除鸦胆子素外)存在交叉耐药。P388/ADR对抗代谢物和烷化剂敏感。还观察到对几种作用机制尚未明确的药物(ICRF - 159、一种对苯二甲酰苯胺、紫杉醇、淋巴细胞肉瘤素、布法丁以及海南狗牙花粗提物)存在交叉耐药。这一观察结果已被证明有助于为确定其中一些药物的作用机制提供线索。一株对柔红霉素耐药的P388白血病亚系的交叉耐药模式虽然没有得到广泛研究,但似乎与P388/ADR相似。