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[2-氯脱氧腺苷、阿糖胞苷和多柔比星对急性髓系白血病克隆形成细胞增殖的影响]

[Effect of 2-chlorodeoxyadenosine, arabinoside cytosine and doxorubicin on acute myeloid leukemia clonogenic cell proliferation].

作者信息

Sawiński K, Hansz J, Kozłowska-Skrzypczak M

机构信息

Kliniki Hematologii AM w Poznaniu.

出版信息

Acta Haematol Pol. 1995;26(3):279-84.

PMID:8525773
Abstract

We examined the influence of 2-chlorodeoxyadenosine (2-CDA) in concentration 300 nM/l alone and in combination with cytosine arabinoside (ara-C; 10(-7) M/l and doxorubicine (drb; 1 microgram/ml) on the proliferation of acute myeloid leukemia (AML) clonogenic cells (L-CFU) in agar/liquid culture system. After preincubation of blast cells with 2-CDA or ara-C as a single agent the number of colonies was reduced, reaching 70% of control (p < 0.05). Exposure of AML blasts to drb resulted in a greater reduction of L-CFU proliferation than in experiments with 2-CDA or ara-C alone (p < 0.05). Coadministration of 2-CDA in conjunction with ara-C or drb, and additionally with ara-C and drb caused the inhibition of L-CFU growth in comparison with control experiments by 52%, 78% and 61%, respectively (p < 0.05). In further experiments we studied the effect of ara-C and drb together with 2-CDA in different concentrations (20, 100 or 300 nM/l). After preincubation with 2-CDA in concentration 20 nM/l no change in blast colony formation was observed in relation to controls which comprised ara-C and drb only (p < 0.05). The increase of 2-CDA concentration to 100 or 300 nM/l in combination with ara-C and drb significantly reduced the growth of AML clonogenic cells (p < 0.05). The greatest, 90%, inhibition of L-CFU proliferation was observed after the exposure of blast cells to ara-C, drb and 2-CDA in concentration 300 nM/l (p < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们在琼脂/液体培养系统中研究了浓度为300 nM/l的2-氯脱氧腺苷(2-CDA)单独以及与阿糖胞苷(ara-C;10⁻⁷ M/l)和阿霉素(drb;1微克/毫升)联合使用对急性髓系白血病(AML)克隆形成细胞(L-CFU)增殖的影响。用2-CDA或ara-C作为单一药物对原始细胞进行预孵育后,集落数量减少,降至对照组的70%(p < 0.05)。将AML原始细胞暴露于drb导致L-CFU增殖的减少比单独使用2-CDA或ara-C的实验更显著(p < 0.05)。与对照实验相比,2-CDA与ara-C或drb联合给药,以及与ara-C和drb同时给药分别导致L-CFU生长抑制52%、78%和61%(p < 0.05)。在进一步的实验中,我们研究了不同浓度(20、100或300 nM/l)的ara-C和drb与2-CDA一起的作用。用浓度为20 nM/l的2-CDA预孵育后,与仅包含ara-C和drb的对照组相比,原始细胞集落形成没有变化(p < 0.05)。2-CDA浓度增加到100或300 nM/l并与ara-C和drb联合使用时,显著降低了AML克隆形成细胞的生长(p < 0.05)。将原始细胞暴露于浓度为300 nM/l的ara-C、drb和2-CDA后,观察到L-CFU增殖的最大抑制,为90%(p < 0.05)。(摘要截断于250字)

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