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维拉帕米增强长春新碱和阿霉素对P388白血病及其长春新碱和阿霉素耐药亚系的细胞毒性作用。

Enhancement of vincristine- and adriamycin-induced cytotoxicity by verapamil in P388 leukemia and its sublines resistant to vincristine and adriamycin.

作者信息

Tsuruo T, Iida H, Yamashiro M, Tsukagoshi S, Sakurai Y

出版信息

Biochem Pharmacol. 1982 Oct 1;31(19):3138-40. doi: 10.1016/0006-2952(82)90097-1.

Abstract

A calcium antagonist, verapamil, enhanced the cellular uptake and cytotoxicity of vincristine (VCR) in adriamycin-resistant P388 leukemia (P388/ADM) cells and also enhanced the cellular uptake and cytotoxicity of adriamycin (ADM) in vincristine-resistant P388 leukemia (P388/VCR) and P388/ADM cells. The enhancement of cytotoxicity and cellular uptake of VCR in P388 and P388/VCR cells has been reported previously. [1]. VCR and ADM resistance was circumvented by verapamil. A common transport mechanism for VCR and ADM, which is responsive to verapamil, seems to exist in VCR- and ADM-resistant cells. However, the enhancement of ADM cytotoxicity and cellular uptake by verapamil was not evident in P388 cells.

摘要

钙拮抗剂维拉帕米可增强阿霉素耐药的P388白血病(P388/ADM)细胞对长春新碱(VCR)的细胞摄取及细胞毒性,还可增强长春新碱耐药的P388白血病(P388/VCR)细胞及P388/ADM细胞对阿霉素(ADM)的细胞摄取及细胞毒性。此前已有报道称维拉帕米可增强P388和P388/VCR细胞对VCR的细胞毒性及细胞摄取[1]。维拉帕米可克服VCR和ADM耐药。VCR和ADM耐药细胞中似乎存在一种对维拉帕米有反应的VCR和ADM共同转运机制。然而,维拉帕米对P388细胞ADM细胞毒性及细胞摄取的增强作用并不明显。

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