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阿霉素耐药的Friend白血病细胞对罗丹明123耐药性的逆转

Reversal of resistance to rhodamine 123 in adriamycin-resistant Friend leukemia cells.

作者信息

Lampidis T J, Munck J N, Krishan A, Tapiero H

出版信息

Cancer Res. 1985 Jun;45(6):2626-31.

PMID:3986800
Abstract

Pleiotropic resistance to rhodamine 123 (Rho-123) in Adriamycin (ADM)-resistant Friend leukemia cells was circumvented by cotreatment with 10 microM verapamil. Increased cytotoxicity corresponded to higher intracellular Rho-123 levels. The verapamil-induced increase of drug accumulation in resistant cells is accounted for at least in part by the blockage or slowing of Rho-123 efflux from these cells. In contrast, accumulation and consequent cytotoxicity of Rho-123 in sensitive cells are not increased by verapamil. Similar results were obtained when ADM was used in this cell system. These results suggest that the efflux system for Rho-123 and ADM in sensitive cells is either reduced or absent. Although Rho-123 accumulates specifically in mitochondria and ADM mainly in the nucleus, the loss of these two different classes of compounds from resistant cells appears to occur via a similar or common mechanism. The similarities in drug transport between Rho-123 and ADM may have important implications when applied to an in vivo environment.

摘要

通过与10微摩尔维拉帕米联合处理,可克服阿霉素(ADM)耐药的Friend白血病细胞对罗丹明123(Rho-123)的多药耐药性。细胞毒性增加与细胞内Rho-123水平升高相对应。维拉帕米诱导耐药细胞中药物蓄积增加,这至少部分是由于Rho-123从这些细胞中的流出受阻或减慢。相反,维拉帕米不会增加Rho-123在敏感细胞中的蓄积及随之而来的细胞毒性。当在该细胞系统中使用ADM时,也获得了类似结果。这些结果表明,敏感细胞中Rho-123和ADM的流出系统要么减少要么不存在。尽管Rho-123特异性蓄积在线粒体中,而ADM主要蓄积在细胞核中,但这两类不同化合物从耐药细胞中的丢失似乎是通过相似或共同的机制发生的。Rho-123和ADM在药物转运方面的相似性在应用于体内环境时可能具有重要意义。

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