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作 者:谢月[1] 李砚如 赵慧慧[1] 黄佳瑜[1] 连芸[1] 朱雨[1] 洪鸣[1] 朱晗[1] 钱思轩[1]
机构地区:[1]江苏省人民医院、南京医科大学第一附属医院血液科,南京210029
出 处:《临床血液学杂志》2017年第3期364-367,共4页Journal of Clinical Hematology
基 金:国家自然科学基金(No:81570143、81270614、81070437)
摘 要:目的:研究地西他滨(DAC)和阿糖胞苷(Ara-C)单用或联合作用对人急性髓细胞白血病HL60细胞增殖的影响,并探讨最佳的联合给药方式。方法:将不同浓度的DAC和Ara-C分别单独或联合作用于HL60细胞,采用CCK8法检测2种药物单独或联合作用对HL60细胞增殖的影响,采用金(正均)氏公式计算协同系数Q值分析两药的协同作用。结果:DAC和Ara-C单独作用时对HL60细胞增殖的抑制作用均呈剂量依赖关系,DAC(0.13~2.00μmol/L)序贯Ara-C联用对HL60细胞增殖抑制有协同作用(Q值为1.20~1.54),并呈剂量依赖性。DAC同时联合Ara-C或Ara-C序贯DAC无协同作用,甚至为拮抗作用(Q值<1.15)。且DAC序贯Ara-C对HL60细胞的增殖抑制率明显高于DAC同时联合Ara-C或Ara-C序贯DAC(P<0.05)。结论:DAC序贯Ara-C可协同抑制HL60细胞增殖,该方案明显优于DAC与Ara-C同时用药组或Ara-C序贯DAC组。DAC48h后序贯Ara-C联合方案在急性髓细胞白血病的治疗中可能具有重要临床意义。Objective:To investigate the inhibitory effects of decitabine (DAC),cytarabine (Ara-C) and their combination on the proliferation of human acute myeloid leukemia HL60 cells in vitro, and to explore the best drug regimen. Method:The cell proliferation inhibitory rates of HL60 cells treated with different concentrations of DAC and Ara-C alone and given either simuhaneously or sequentially were detected by CCK8 assay. King formula was used to determine if there was a synergistic effect of DAC in combination with Ara-C. Result: Both DAC and Ara-C as single agent had dose-dependent effects of proliferation inhibition on HL60 cells. DAC (0.13 to 2.00 μmol/L) prior to Ara-C had a synergistic effect on proliferation inhibition (Q value was 1.20 to 1.54). DAC and Ara-C giv en simultaneously and Ara-C prior to DAC had no synergistic effect, or even antagonism (Q value〈1.15). DAC prior to Ara-C showed the highest proliferation inhibition rate compared with DAC and Ara-C given simuhaneously and Ara-C prior to DAC (P〈0.05). Conclusion:DAC followed by Ara C is a best synergistic combination in HL60 cell line compared with DAC and Ara-C given simultaneously and Ara-C prior to DAC. It suggests that DAC followed by Ara-C48 hours later may have great clinical potential in the treatment of acute myeloid leukemia.
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