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细胞松弛素和秋水仙碱对耐药肿瘤细胞中柔红霉素和长春新碱蓄积及滞留的影响。

Effects of cytochalasins and colchicine on the accumulation and retention of daunomycin and vincristine in drug resistant tumor cells.

作者信息

Tsuruo T, Iida H

出版信息

Biochem Pharmacol. 1986 Apr 1;35(7):1087-90. doi: 10.1016/0006-2952(86)90143-7.

Abstract

Cytochalasin B and D enhanced vincristine (VCR) and daunomycin (DAU) accumulation in tumor cells, especially in VCR- and DAU-resistant cell lines. The effect of cytochalasin B, and to a lesser extent cytochalasin D, was almost equivalent to that observed for verapamil, a calcium channel blocker which has been reported to enhance drug accumulation in tumor cells. Cytochalasin B was most effective in VCR- and DAU-sensitive cells; however, the effect in resistant cells was less than that observed for verapamil, suggesting a different mode of action between these drugs in sensitive and resistant cells. Enhanced accumulation of VCR and DAU by cytochalasins was mediated by the inhibition of outward transport of VCR and DAU from tumor cells. Colchicine had no effect on VCR and DAU accumulation. Cytochalasins, especially cytochalasin D is a specific inhibitor of microfilament assembly in cells. These results indicate that the cellular microfilament system plays a prominent role in drug transport of tumor cells, and that an intact microtubular system is less involved.

摘要

细胞松弛素B和D可增强肿瘤细胞中长春新碱(VCR)和柔红霉素(DAU)的蓄积,尤其是在对VCR和DAU耐药的细胞系中。细胞松弛素B的作用,以及程度稍小的细胞松弛素D的作用,几乎等同于维拉帕米(一种钙通道阻滞剂,据报道可增强肿瘤细胞中的药物蓄积)所观察到的效果。细胞松弛素B在对VCR和DAU敏感的细胞中最为有效;然而,其在耐药细胞中的作用小于维拉帕米,这表明这些药物在敏感细胞和耐药细胞中的作用方式不同。细胞松弛素增强VCR和DAU的蓄积是通过抑制VCR和DAU从肿瘤细胞的外向转运介导的。秋水仙碱对VCR和DAU的蓄积没有影响。细胞松弛素,尤其是细胞松弛素D是细胞中微丝组装的特异性抑制剂。这些结果表明,细胞微丝系统在肿瘤细胞的药物转运中起重要作用,而完整的微管系统参与较少。

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