ACS Chem Biol. 2013 May 17;8(5):884-9. doi: 10.1021/cb300641h. Epub 2013 Feb 22.
Glaziovianin A, an isoflavone isolated from the leaves of Ateleia glazioviana, inhibits the cell cycle progression in M-phase with an abnormal spindle structure, but its inhibitory mechanism has not been revealed. Here, we report that glaziovianin A and its derivatives are microtubule dynamics inhibitors. Glaziovianin A extended the time lag of tubulin polymerization without changing the net amount of polymerized tubulin in vitro and suppressed microtubule dynamics in cells. Furthermore, glaziovianin A inhibited the transport of endosomes containing EGF-stimulated EGFR and prolonged the EGFR activation. Consistent with the prolonged activation of EGFR, glaziovianin A enhanced the EGF-dependent apoptosis in A431 cells. These results strongly suggested that microtubule dynamics is important for endosome transport and maturation, and that glaziovianin A shows cytotoxicity by two pathways, the mitotic arrest and inadequate activation of receptor kinases via the inhibition of endosome maturation.
从 Ateleia glazioviana 的叶子中分离得到的异黄酮 Glaziovianin A,能够抑制有异常纺锤体结构的 M 期细胞周期进程,但它的抑制机制尚未被揭示。在这里,我们报告称 Glaziovianin A 及其衍生物是微管动力学抑制剂。Glaziovianin A 在体外延长了微管聚合的时间滞后,而不改变聚合微管的总量,并抑制了细胞中的微管动力学。此外,Glaziovianin A 抑制了含有 EGF 刺激的 EGFR 的内体的运输,并延长了 EGFR 的激活。与 EGFR 的激活延长一致,Glaziovianin A 增强了 A431 细胞中 EGF 依赖性的细胞凋亡。这些结果强烈表明,微管动力学对于内体运输和成熟很重要,并且 Glaziovianin A 通过两种途径显示出细胞毒性,即通过抑制内体成熟来导致有丝分裂阻滞和受体激酶的激活不足。