Gibby E M, Boyse O, Hill B T
Cancer Chemother Pharmacol. 1987;20(1):5-7. doi: 10.1007/BF00252950.
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.
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。