Foa P, Maiolo A T, Lombardi L, Villa L, Polli E E
Scand J Haematol. 1986 Jan;36(1):107-10. doi: 10.1111/j.1600-0609.1986.tb02659.x.
Deferoxamine is a hydroxylamine which binds ferric ions to form a highly stable complex. Since iron is thought to be required at a critical stage for cell proliferation, we investigated the effect of deferoxamine on the proliferative activity of human leukaemic cell populations in vitro by means of 3 permanent cell lines, HL60, U937 and 8402. We found deferoxamine to be a potent inhibitor of DNA synthesis and proliferation of leukaemic cells, acting by accumulating treated cells at the early S phase of the cell cycle. Suppression of leukaemic proliferation was obtained at deferoxamine concentrations in the range usually achieved in the treatment of patients for iron overload. Deferoxamine might therefore warrant further investigation as a potentially useful agent for leukaemia chemotherapy.
去铁胺是一种羟胺,它能与铁离子结合形成高度稳定的复合物。由于人们认为在细胞增殖的关键阶段需要铁,我们通过3种永久性细胞系HL60、U937和8402,研究了去铁胺在体外对人白血病细胞群体增殖活性的影响。我们发现去铁胺是白血病细胞DNA合成和增殖的有效抑制剂,其作用机制是使处理后的细胞在细胞周期的早期S期积累。在通常用于治疗患者铁过载的去铁胺浓度范围内,可抑制白血病细胞增殖。因此,去铁胺作为一种潜在有用的白血病化疗药物,可能值得进一步研究。