Chou S, Kaneko M, Nakaya K, Nakamura Y
School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.
Biochem Biophys Res Commun. 1990 Jan 15;166(1):160-7. doi: 10.1016/0006-291x(90)91925-i.
Low concentrations of camptothecin induced differentiation of human and mouse myeloid leukemia cells including human HL60, U937, ML1, and K562 cells and mouse M1 cells as measured by various differentiation-associated properties. When K562 cells were pretreated with 20 nM camptothecin for 2 h, 53% of the cells were induced to differentiate as measured by NBT staining. Significant single strand breaks in DNA of K562 cells were caused by this treatment. Most single strand breaks were accompanied by protein-DNA cross linking. The combination of camptothecin and rTNF synergistically induced differentiation of human ML1, U937, and M1 cells. These results suggest that topo I may be important in some differentiation of myeloid leukemia cells.
低浓度喜树碱可诱导人源和鼠源髓系白血病细胞分化,包括人HL60、U937、ML1和K562细胞以及鼠M1细胞,这可通过多种与分化相关的特性来衡量。当用20 nM喜树碱预处理K562细胞2小时后,通过NBT染色测定,53%的细胞被诱导分化。这种处理导致K562细胞的DNA出现显著单链断裂。大多数单链断裂伴有蛋白质-DNA交联。喜树碱与rTNF联合可协同诱导人ML1、U937和M1细胞分化。这些结果表明拓扑异构酶I在髓系白血病细胞的某些分化过程中可能很重要。