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维拉帕米及其他药物对蒽环类药物分布和耐药逆转的影响。

Effect of verapamil and other agents on the distribution of anthracyclines and on reversal of drug resistance.

作者信息

Hindenburg A A, Baker M A, Gleyzer E, Stewart V J, Case N, Taub R N

出版信息

Cancer Res. 1987 Mar 1;47(5):1421-5.

PMID:3469017
Abstract

We studied the intracellular distribution of drugs within anthracycline-sensitive and -resistant cells by computer-assisted digitized video fluorescence microscopy. We found that the antitumor antibiotic, daunorubicin, distributes differently in anthracycline-sensitive and -resistant human leukemia cells (HL-60). Verapamil and other agents known to circumvent resistance in pleiotropic drug-resistant cell lines were able to change the pattern of distribution of daunorubicin in the anthracycline-resistant HL-60 cells back to the distribution found in anthracycline-sensitive HL-60 cells. To investigate the biochemical basis for this effect, we studied the distribution of daunorubicin and doxorubicin in a hydrophobic/hydrophilic (membrane/cytoplasmic) environment using the two-compartment cell-free system of Folch. Our results demonstrate that various unrelated drugs known to overcome resistance will also change the distribution of the anthracyclines in the hydrophobic/hydrophilic compartments. Our data allow the hypothesis that various unrelated agents known to circumvent resistance may act by altering the hydrophobic/hydrophilic solubility of anthracyclines in the resistant cell.

摘要

我们通过计算机辅助数字化视频荧光显微镜研究了蒽环类药物敏感和耐药细胞内药物的分布情况。我们发现,抗肿瘤抗生素柔红霉素在蒽环类药物敏感和耐药的人类白血病细胞(HL-60)中的分布不同。维拉帕米和其他已知能克服多药耐药细胞系耐药性的药物能够使柔红霉素在蒽环类药物耐药的HL-60细胞中的分布模式恢复到蒽环类药物敏感的HL-60细胞中的分布。为了研究这种效应的生化基础,我们使用Folch的两室无细胞系统研究了柔红霉素和阿霉素在疏水/亲水(膜/细胞质)环境中的分布。我们的结果表明,各种已知能克服耐药性的无关药物也会改变蒽环类药物在疏水/亲水隔室中的分布。我们的数据支持这样一种假设,即各种已知能规避耐药性的无关药物可能通过改变蒽环类药物在耐药细胞中的疏水/亲水性溶解度来发挥作用。

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