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维拉帕米与蒽醌类药物在阿霉素敏感及耐药的小鼠和人肿瘤细胞系中的体外选择性相互作用。

Selective interactions of verapamil with anthraquinones in adriamycin-sensitive and -resistant murine and human tumour cell lines in vitro.

作者信息

Gibby E M, Boyse O, Hill B T

出版信息

Cancer Chemother Pharmacol. 1987;20(1):5-7. doi: 10.1007/BF00252950.

Abstract

Enhancement of the cytotoxicity of adriamycin (ADR) by addition of verpamil (VPM) was selective and, in part, concentration-dependent. In an ADR-resistant murine L5178Y lymphoma subline sensitivity was improved with ADR and 1 microM VPM, whereas the cytotoxic effects of mitoxantrone or esorubicin were not affected by VPM. In human ovarian SK-OV-3 tumour cells ADR cytotoxicity was only enhanced by 6.6 microM VPM and there was no selective advantage against an ADR-resistant subline. Circumvention of ADR resistance by VPM is not a universal phenomenon, appearing least effective against sublines expressing relatively low orders of resistance, which may be those most commonly encountered clinically.

摘要

加入维拉帕米(VPM)可增强阿霉素(ADR)的细胞毒性,这种增强具有选择性,且部分呈浓度依赖性。在对阿霉素耐药的小鼠L5178Y淋巴瘤亚系中,阿霉素与1微摩尔/升的维拉帕米联用可提高敏感性,而米托蒽醌或表柔比星的细胞毒性不受维拉帕米影响。在人卵巢SK-OV-3肿瘤细胞中,仅6.6微摩尔/升的维拉帕米可增强阿霉素的细胞毒性,且对阿霉素耐药亚系无选择性优势。维拉帕米克服阿霉素耐药并非普遍现象,对表达相对低水平耐药性的亚系效果最差,而这些亚系可能是临床上最常见的。

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