克隆形成试验
医学
药理学
体外
阿糖胞苷
柔红霉素
去铁胺
细胞生长
细胞培养
细胞周期
生长抑制
甲氨蝶呤
癌症研究
白血病
免疫学
生物化学
生物
内科学
癌症
遗传学
作者
Zeev Estrov,A Cohen,Erwin W. Gelfand,Melvin H. Freedman
标识
DOI:10.1097/00043426-198824000-00003
摘要
Deferoxamine (DFO), a widely used therapeutic iron chelator, was found to inhibit proliferation of the promyelocytic leukemia cell line HL-60 in a dose-dependent fashion when tested in a clonogenic assay at concentrations ranging from 1.0 to 10.0 microM. Cytosine arabinoside, methotrexate, and daunorubicin also produced dose-dependent inhibition of HL-60 colony growth when tested singly in vitro. When DFO, 1.0 microM, was included with each agent in dose-response studies, a synergistic enhancement of the antiproliferative effects was observed. This synergism probably results from a DFO-induced decrease in intracellular levels of deoxyribonucleoside triphosphates and an inhibition of the cells at the early S-phase of cell cycle. Our data suggest that DFO has potential as an adjunctive antileukemic agent.
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