College of Science and Technology, Nihon University, 1–8–14 Kanda Surugadai, Chiyoda-ku, Tokyo 101–8308, Japan.
Biol Pharm Bull. 2013;36(1):135-9. doi: 10.1248/bpb.b12-00795.
12-O-Acetylazedarachin B (1), isolated from the fruit extract of Melia azedarach, exhibited potent cytotoxicity against leukemia (HL-60) (IC(50) 0.016 µM) and stomach (AZ521) (IC(50) 0.035 µM) cancer cell lines. Upon assessing the apoptosis-inducing activity in HL-60 cells, compound 1 exhibited induction of apoptosis detected by the observation of membrane phospholipid exposure and DNA fragmentation in flow cytometry. Western blot analysis showed that 1 markedly reduced the levels of procaspases-3, 8, and 9, while being increased the levels of cleaved caspases-3, 8, and 9. In addition, compound 1 increased significantly Bax/Bcl-2 ratio. These results suggested that 1 induced apoptotic cell death in HL-60 via both mitochondrial and death receptor-mediated pathways. Therefore, compound 1 may be promising lead compound for developing an effective drug for treatment of leukemia. Flow cytometric analysis suggested that the cytotoxicity of 1 against AZ521 is due to inducing apoptosis as well as necrosis with the latter predominated.
12-O-乙酰川楝素 B(1)从川楝果实提取物中分离得到,对白血病(HL-60)(IC50 为 0.016 μM)和胃癌(AZ521)(IC50 为 0.035 μM)细胞系表现出很强的细胞毒性。在评估 1 在 HL-60 细胞中的诱导凋亡活性时,通过观察流式细胞术检测到细胞膜磷脂暴露和 DNA 片段化,发现化合物 1 诱导了凋亡。Western blot 分析表明,1 显著降低了 procaspases-3、8 和 9 的水平,同时增加了 cleaved caspases-3、8 和 9 的水平。此外,化合物 1 显著增加了 Bax/Bcl-2 比值。这些结果表明,1 通过线粒体和死亡受体介导的途径诱导 HL-60 细胞发生凋亡性细胞死亡。因此,化合物 1 可能是开发治疗白血病有效药物的有前途的先导化合物。流式细胞术分析表明,1 对 AZ521 的细胞毒性既诱导了凋亡,也诱导了坏死,后者占主导地位。