阿糖胞苷
标志(线性代数)
氟达拉滨
髓系白血病
癌基因
细胞毒性
生物
细胞周期
药理学
髓样
白血病
分子医学
癌症研究
体外
细胞凋亡
肿瘤科
医学
免疫学
内科学
化疗
环磷酰胺
遗传学
数学
纯数学
域代数上的
作者
Isabelle Hubeek,Е. Г. Литвинова,Godefridus J. Peters,Richard Broekhuizen,Eric G. Haarman,D. R. Huismans,Jacqueline Cloos,C. Michel Zwaan,Gudrun Fleischhack,Ursula Creutzig,Gertjan J.L. Kaspers
标识
DOI:10.3892/ijo.25.6.1823
摘要
The combination of fludarabine, cytarabine (ara-C) and G-CSF (FLAG) is routinely used in the treatment of acute myeloid leukemia (AML). In this study we characterized the interactions between fludarabine, ara-C and G-CSF in vitro using AML blasts. Exposure to G-CSF alone resulted in a higher leukemic cell survival (LCS), which might be indicative of increased proliferation. The LCS decreased significantly from 69.7 to 54.0% when blasts were exposed to G-CSF 21 h prior to incubation with ara-C (p=0.01). In contrast, LCS increased significantly (from 55.6 to 69.0%; p=0.04) after sequential exposure to G-CSF and fludarabine. Exposure to 4 combinations of fludarabine (4 h; 0.14 microM and 0.55 microM) and ara-C (96 h; 0.21 and 0.82 microM) (FLA) resulted in additive cytotoxicity. The triple combination (FLAG), 21 h 5 microM G-CSF followed by 4 h fludarabine (0.14 and 0.55 microM) and finally ara-C (0.21 and 0.82 microM) for 96 h also resulted in an additive cell kill. In conclusion, these data support the clinical use of G-CSF in combination with ara-C, and the combination of ara-C and FLA. Pre-exposure to G-CSF before FLA (FLAG) did not result in increased cytotoxicity in our experiments, indicative of similar anti-leukemic activity.
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