Baez A, Sepulveda J
Department of Pharmacology, School of Medicine, University of Puerto Rico, Juan 00936-5067.
Leuk Res. 1992;16(4):363-70. doi: 10.1016/0145-2126(92)90138-w.
Drugs which elicit cell differentiation might have an important role in the treatment of leukemias and other neoplasias. Various chemotherapeutic agents promote leukemic cell differentiation. The HL-60 cell line is a useful model to study in vitro myeloid differentiation. Sublethal concentrations of 3-nitrobenzothiazolo[3,2-a]quinolinium (NBQ), an antitopoisomerase II drug, were given to HL-60 cells from one to five days to evaluate its capacity to induce differentiation. NBQ-induced HL-60 cells reduced nitroblue tetrazolium (NBT), increased MY-4 receptors, increased phagocytic activity and displayed the granulocytic morphology. Flow cytometric DNA analysis of NBQ-induced cells revealed an arrest in the G1 phase a reduction in the relative percentage of cells in S and G2+M phases. Our results suggest that NBQ induces an S-phase specific differentiation of HL-60 cells comparable to that previously described with dimethyl sulfoxide and retinoic acid. NBQ and its analogs, as differentiation inducers, may have potential utility as a novel therapeutic modality for leukemias.
能够引发细胞分化的药物可能在白血病和其他肿瘤的治疗中发挥重要作用。多种化疗药物可促进白血病细胞分化。HL-60细胞系是研究体外髓系分化的有用模型。将亚致死浓度的3-硝基苯并噻唑并[3,2-a]喹啉鎓(NBQ,一种抗拓扑异构酶II药物)作用于HL-60细胞1至5天,以评估其诱导分化的能力。NBQ诱导的HL-60细胞使硝基蓝四氮唑(NBT)还原,增加MY-4受体,增强吞噬活性并呈现粒细胞形态。对NBQ诱导的细胞进行流式细胞术DNA分析显示,细胞停滞于G1期,S期和G2+M期细胞的相对百分比降低。我们的结果表明,NBQ诱导HL-60细胞发生S期特异性分化,这与之前用二甲基亚砜和视黄酸所描述的情况相当。NBQ及其类似物作为分化诱导剂,可能具有作为白血病新型治疗方式的潜在用途。