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多药耐药性:胆固醇流出途径起作用吗?

Multidrug resistance: a role for cholesterol efflux pathways?

作者信息

Liscovitch M, Lavie Y

机构信息

Dept of Biological Regulation, Weizmann Institute of Science, 76100, Rehovot, Israel.

出版信息

Trends Biochem Sci. 2000 Nov;25(11):530-4. doi: 10.1016/s0968-0004(00)01668-6.

Abstract

Multidrug resistance (MDR) severely impairs the efficacy of cancer chemotherapy. Several protein transporters that mediate drug export have been identified, but additional adaptations appear to be necessary for full-fledged drug resistance. The cell surface density of caveolae and the expression of the caveolar coat protein caveolin are dramatically increased in MDR cancer cells. Acquisition of MDR might thus be accompanied by upregulation of caveolin-dependent cholesterol efflux pathways, raising the possibility that these same pathways are utilized for delivering drugs from intracellular compartments to the plasma membrane, where drugs can be extruded from the cells by drug efflux ATPases. The upregulation of caveolin mandates a phenotypic change of MDR cells in terms of their cholesterol homeostasis and is accompanied by loss of important features of the transformed phenotype of MDR cancer cells.

摘要

多药耐药性(MDR)严重损害癌症化疗的疗效。已鉴定出几种介导药物外排的蛋白质转运体,但似乎还需要其他适应性变化才能实现完全的耐药性。在MDR癌细胞中,小窝的细胞表面密度和小窝衣被蛋白小窝蛋白的表达显著增加。因此,获得MDR可能伴随着小窝蛋白依赖性胆固醇流出途径的上调,这增加了一种可能性,即这些相同的途径被用于将药物从细胞内区室转运到质膜,在质膜处药物可以通过药物外排ATP酶从细胞中排出。小窝蛋白的上调要求MDR细胞在胆固醇稳态方面发生表型变化,并伴随着MDR癌细胞转化表型的重要特征丧失。

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