Higashigawa M, Ido M, Ohkubo T, Kawasaki H, Kamiya H, Sakurai M, Taniguchi K, Hamazaki M
Department of Pediatrics, Mie University School of Medicine, Japan.
Leuk Res. 1989;13(1):39-42. doi: 10.1016/0145-2126(89)90029-5.
A variant P388 murine leukemic cell resistant to 4'-demethylepipodophyllotoxin-9-(4,6-O-ethylidine)-beta-D-gl ucopyranoside (etoposide) (VP-16-213) was cloned. The variant P388/VP-16 cell line was 159-fold resistant to VP-16. We found that this variant P388/VP-16 cell line showed collateral drug sensitivity to 1-beta-D-arabinofuranosylcytosine(Ara-C), determined by comparing the 50% inhibitory concentrations in 48-h growth inhibition assay. To clarify the mechanism of this increased sensitivity to Ara-C, we quantified the deoxyribonucleoside triphosphate pools and 1-beta-D-arabinofuranosylcytosine triphosphate(Ara-CTP) using high-performance liquid chromatography in the parent and drug-resistant sublines of P388 cells. The analysis of deoxyribonucleoside triphosphate pools revealed that the pyrimidine triphosphate pools were significantly decreased in the P388/VP-16 cell line and the Ara-CTP concentration of two variant cell lines were not significantly different. The Ara-CTP/dCTP ratio was significantly increased in P388/VP-16 cells. These data suggest that the inhibition of the dCTP de-novo pathway and the preservation of the dCTP salvage pathway in P388/VP-16 cells might correlate with the increased sensitivity to Ara-C.
克隆出一株对4'-去甲基表鬼臼毒素-9-(4,6-O-亚乙基)-β-D-葡萄糖苷(依托泊苷)(VP-16-213)耐药的变异型P388鼠白血病细胞。变异型P388/VP-16细胞系对VP-16的耐药性是原来的159倍。我们发现,通过比较48小时生长抑制试验中的50%抑制浓度,该变异型P388/VP-16细胞系对1-β-D-阿拉伯呋喃糖基胞嘧啶(阿糖胞苷)表现出协同药物敏感性。为阐明对阿糖胞苷敏感性增加的机制,我们使用高效液相色谱法对P388细胞的亲代和耐药亚系中的脱氧核苷三磷酸池和1-β-D-阿拉伯呋喃糖基胞嘧啶三磷酸(阿糖胞苷三磷酸)进行了定量分析。脱氧核苷三磷酸池的分析显示,P388/VP-16细胞系中的嘧啶三磷酸池显著减少,且两个变异细胞系的阿糖胞苷三磷酸浓度无显著差异。P388/VP-16细胞中的阿糖胞苷三磷酸/脱氧胞苷三磷酸比值显著增加。这些数据表明,P388/VP-16细胞中脱氧胞苷三磷酸从头合成途径的抑制和脱氧胞苷三磷酸补救途径的保留可能与对阿糖胞苷敏感性增加有关。