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阿霉素在胰腺癌耐药和敏感模型中的细胞药理学比较。

Comparison of the cellular pharmacology of doxorubicin in resistant and sensitive models of pancreatic cancer.

作者信息

Chang B K, Gregory J A

出版信息

Cancer Chemother Pharmacol. 1985;14(2):132-4. doi: 10.1007/BF00434351.

Abstract

The cellular accumulation and retention of doxorubicin (ADR) was investigated in two models of pancreatic adenocarcinoma, which differ markedly in their sensitivity to ADR. In vitro studies revealed that the relatively resistant cell line, WD PaCa (or well-differentiated pancreatic adenocarcinoma of the Syrian hamster), actually had higher ADR cellular levels than the sensitive cell line, PD PaCa (or poorly differentiated pancreatic adenocarcinoma of the Syrian hamster). While the efflux of ADR from WD PaCa was greater, the overall retention of ADR by WD PaCa was comparable to PD PaCa. These results failed to document differences in accumulation or retention of ADR capable of explaining the difference in the sensitivity of the cell lines to ADR and indicate the need to search beyond attainable drug concentrations for mechanisms of primary ADR resistance.

摘要

在两种对阿霉素(ADR)敏感性差异显著的胰腺腺癌模型中,研究了阿霉素(ADR)的细胞蓄积和滞留情况。体外研究表明,相对耐药的细胞系WD PaCa(或叙利亚仓鼠的高分化胰腺腺癌),其ADR细胞水平实际上高于敏感细胞系PD PaCa(或叙利亚仓鼠的低分化胰腺腺癌)。虽然WD PaCa中ADR的外排更大,但WD PaCa对ADR的总体滞留与PD PaCa相当。这些结果未能证明ADR在蓄积或滞留方面的差异能够解释细胞系对ADR敏感性的差异,并表明需要在可达到的药物浓度之外寻找原发性ADR耐药的机制。

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