Jachez B, Boesch D, Emmer G, Loor F
Sandoz Pharma Ltd., Basel, Switzerland.
Anticancer Drugs. 1994 Jun;5(3):313-20.
Tumor cells whose multidrug resistance is caused by the P-glycoprotein (Pgp) mediated anti-cancer drug (ACD) efflux can be chemosensitized by cyclosporins, whose derivatives were found to display a whole range of resistance-modulating activities. Similarly, derivatives of the non-immunosuppressive natural fungus cyclic peptolide SDZ 90-215 were recently shown to display a broad range of chemosensitizing activities. With highly resistant cells expressing high levels of Pgp, one such compound (SDZ 280-125) was shown here to restore both a normal sensitivity to the growth-inhibitory effects of ACD and a normal retention of an anthracycline antibiotic. With both read-outs, SDZ 280-125 activity was about 3-fold that of cyclosporin A (CsA). SDZ 280-125 also displayed the same profile of chemosensitization as CsA for different ACD classes.
由P-糖蛋白(Pgp)介导的抗癌药物(ACD)外排导致多药耐药的肿瘤细胞可被环孢菌素化学增敏,其衍生物具有一系列耐药调节活性。同样,非免疫抑制性天然真菌环肽SDZ 90-215的衍生物最近也显示出广泛的化学增敏活性。对于高表达Pgp的高耐药细胞,本文展示了一种这样的化合物(SDZ 280-125)既能恢复对ACD生长抑制作用的正常敏感性,又能恢复蒽环类抗生素的正常潴留。在这两种检测指标上,SDZ 280-125的活性约为环孢菌素A(CsA)的3倍。对于不同类别的ACD,SDZ 280-125也显示出与CsA相同的化学增敏特征。