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白血病P388细胞中可能存在两种导致蒽环类药物耐药的独立机制。

Possible coexistence of two independent mechanisms contributing to anthracycline resistance in leukaemia P388 cells.

作者信息

Soto F, Planells-Cases R, Canaves J M, Ferrer-Montiel A V, Aleu J, Gamarro F, Castanys S, Gonzalez-Ros J M, Ferragut J A

机构信息

Department of Neurochemistry, University of Alicante, Spain.

出版信息

Eur J Cancer. 1993;29A(15):2144-50. doi: 10.1016/0959-8049(93)90050-p.

Abstract

Murine leukaemia P388 and L1210 cell sublines with varying degrees of resistance to the anthracycline daunomycin (DNM) have been used to monitor (i) intracellular accumulation of DNM, (ii) expression of the drug efflux pump P-glycoprotein (pgp) and (iii) cytoplasmic pH changes. Drug-resistant L1210/65 cells (65-fold resistance), overexpress pgp, and display decreased intracellular accumulation of DNM and identical intracellular pH as compared to the parental drug-sensitive L1210 cell line. On the other hand, moderately drug-resistant P388/20 cells (20-fold resistance), which also exhibit a decreased intracellular drug accumulation with respect to drug-sensitive P388/S cells, display only moderate pgp-encoding mdr1 gene transcription without detectable levels of pgp protein, and undergo cytoplasmic alkalinisation (up to approximately 0.2 pH units). A further increase in the level of drug resistance (P388/100 cells, 100-fold resistance), results in a more pronounced decrease in drug accumulation, significant pgp expression and slightly higher intracellular alkalinisation. Alterations in the degree of protonation of DNM have been shown previously to influence processes such as the rate of uptake and the intracellular accumulation of the drug. On this basis, we propose that the changes in intracellular pH, observed at low levels of drug resistance (P388/20 cells), could constitute an early cellular response aimed at decreasing the intracellular accumulation of ionisable anti-neoplastics. As the level of resistance increases (P388/100), the cells seem to require more efficient mechanisms of defense against the drug, such as that represented by the expression of pgp. Since there is no apparent correlation between the extent of the changes in intracellular pH and the level of pgp expression in DNM-resistant P388 cell sublines, it is suggested that these two cellular responses contributing to drug resistance could operate independently.

摘要

对蒽环类药物柔红霉素(DNM)具有不同程度抗性的小鼠白血病P388和L1210细胞亚系已被用于监测:(i)DNM的细胞内蓄积;(ii)药物外排泵P-糖蛋白(pgp)的表达;以及(iii)细胞质pH变化。耐药的L1210/65细胞(65倍抗性)过表达pgp,与亲本药物敏感的L1210细胞系相比,其DNM的细胞内蓄积减少,且细胞内pH相同。另一方面,中度耐药的P388/20细胞(20倍抗性),相对于药物敏感的P388/S细胞,其细胞内药物蓄积也减少,仅表现出中等程度的pgp编码mdr1基因转录,未检测到pgp蛋白水平,且发生细胞质碱化(高达约0.2个pH单位)。耐药水平进一步升高(P388/100细胞,100倍抗性),导致药物蓄积更显著减少、pgp表达明显增加以及细胞内碱化略高。先前已表明DNM质子化程度的改变会影响药物摄取速率和细胞内蓄积等过程。在此基础上,我们提出在低耐药水平(P388/20细胞)观察到的细胞内pH变化可能构成一种早期细胞反应,旨在减少可电离抗肿瘤药物的细胞内蓄积。随着耐药水平升高(P388/100),细胞似乎需要更有效的药物防御机制,如pgp表达所代表的机制。由于在DNM耐药的P388细胞亚系中,细胞内pH变化程度与pgp表达水平之间没有明显相关性,提示这两种导致耐药的细胞反应可能独立发挥作用。

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