Nagai M, Yamada H, Nakada S, Ochi K, Nemoto T, Takahara S, Hoshina S, Horiguchi-Yamada J
Department of Internal Medicine, Aoto Hospital, Tokyo, Japan.
Mol Cell Biochem. 1995 Mar 23;144(2):191-5. doi: 10.1007/BF00944399.
The antiproliferative effect of roxithromycin (RXM) was studied using human myeloid leukemia HL60 cells. RXM inhibited the growth of HL60 cells in a concentration-dependent manner, and significantly inhibited growth at concentrations above 75 microM. This growth inhibition was not associated with specific cell cycle arrest and DNA synthesis was not impaired. In addition, the number of viable cells remained almost unchanged in the presence of 100 microM RXM. RXM induced growth inhibition at least partly by the formation of multinucleate cells. Both flowcytometric and morphological examination revealed that more than 40% of the RXM-treated cells were binucleate. These findings demonstrate that RXM is a potent new modulator of cell cycle progression in HL60 cells and suggest that the inhibition of cytokinesis by this drug may provide a new model for studying mitosis.
使用人髓性白血病HL60细胞研究了罗红霉素(RXM)的抗增殖作用。RXM以浓度依赖性方式抑制HL60细胞的生长,并且在浓度高于75 microM时显著抑制生长。这种生长抑制与特定的细胞周期停滞无关,并且DNA合成未受损。此外,在存在100 microM RXM的情况下,活细胞数量几乎保持不变。RXM至少部分地通过形成多核细胞诱导生长抑制。流式细胞术和形态学检查均显示,超过40%的经RXM处理的细胞为双核细胞。这些发现表明,RXM是HL60细胞中细胞周期进程的一种有效的新型调节剂,并表明该药物对胞质分裂的抑制作用可能为研究有丝分裂提供一个新模型。