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1-β-D-阿拉伯呋喃糖基胞嘧啶和6-硫鸟嘌呤在体外对粒细胞祖细胞的细胞毒性作用。

Cytotoxic effects of 1-beta-D-arabinofuranosylcytosine and 6-thioguanine in vitro on granulocytic progenitor cells.

作者信息

Greenberg P L, VanKersen I, Mosny S

出版信息

Cancer Res. 1976 Dec;36(12):4412-7.

PMID:1069606
Abstract

We have utilized an in vitro clonogenic assay of mouse and human marrow granulocytic progenitor cells to determine the cytotoxic effects on granulopoiesis of the chemotherapeutic agents 1-beta-D-arabinofuranosylcytosine (ara-C) and 6-thioguanine. Concentration- and time-dependent decrements to plateau levels of granulocytic colony-forming capacity occurred. The sequence of drug administration was important and synergistic cytotoxicity was noted when certain schedules of ara-C and 6-thioguanine combinations were used. Endotoxin-stimulated colony-forming cells had increased sensitivity to the in vitro ara-C exposure. High or intermittent doses of ara-C demonstrated enhanced cytotoxicity when short exposure times (1 to 8 hr) were utilized, whereas low doses were markedly cytotoxic with prolonged exposure (10 days). Normal and leukemic human colony-forming cells had similar susceptibility to the cytotoxic effects of ara-C. Exposure of granulocytic precursors to these drugs in vitro produced effects similar to those previously reported with in vivo drug administration. These techniques appear applicable for providing improved screening models to evaluate chemotherapeutic regimens for clinical use.

摘要

我们利用小鼠和人类骨髓粒细胞祖细胞的体外克隆形成试验,来确定化疗药物1-β-D-阿拉伯呋喃糖基胞嘧啶(阿糖胞苷)和6-硫鸟嘌呤对粒细胞生成的细胞毒性作用。粒细胞集落形成能力出现了浓度和时间依赖性的下降,直至达到平台水平。给药顺序很重要,当使用特定的阿糖胞苷和6-硫鸟嘌呤联合给药方案时,可观察到协同细胞毒性。内毒素刺激的集落形成细胞对体外阿糖胞苷暴露的敏感性增加。当采用短暴露时间(1至8小时)时,高剂量或间歇剂量的阿糖胞苷显示出增强的细胞毒性,而低剂量在长时间暴露(10天)时具有明显的细胞毒性。正常和白血病人类集落形成细胞对阿糖胞苷的细胞毒性作用具有相似的敏感性。粒细胞前体在体外暴露于这些药物所产生的效应,与先前体内给药所报道的效应相似。这些技术似乎适用于提供改进的筛选模型,以评估临床使用的化疗方案。

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