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首页> 外文期刊>Journal of Asian natural products research >Flavonoids from Vitex trifolia L. inhibit cell cycle progression at G2/M phase and induce apoptosis in mammalian cancer cells.
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Flavonoids from Vitex trifolia L. inhibit cell cycle progression at G2/M phase and induce apoptosis in mammalian cancer cells.

机译:Vitri trifolia L.的类黄酮抑制G2 / M期的细胞周期进程并诱导哺乳动物癌细胞的凋亡。

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摘要

Six flavonoids, persicogenin (1), artemetin (2), luteolin (3), penduletin (4), vitexicarpin (5) and chrysosplenol-D (6), have been isolated for the first time as new cell cycle inhibitors from Vitex trifolia L., a Chinese folk medicine used to treat cancers, through a bioassay-guided separation procedure. They were identified by spectroscopic methods. The inhibitory effects of 1-6 on the proliferation of mammalian cancer cells have been evaluated by the SRB (sulforhodamine B) method and their effects on cell cycle and apoptosis investigated by flow cytometry with the morphological observation under light microscope and by agarose-gel electrophoresis to detect internucleosomal DNA fragmentation. Compounds 1-6 inhibited the proliferation of mouse tsFT210 cancer cells with the IC50s (microg ml(-1)) > 100 (inhibition rate at 100 microg ml(-1), 47.9%) for 1, >100 (inhibition rate at 100 microg ml(-1), 49.6 %) for 2, 10.7 for 3, 19.8 for 4, 0.3 for 5, and 3.5 for 6. Flow cytometric investigations for 1-6 demonstrated that 1-5 mainly inhibited cell cycle at the G2/M phase in a dose-dependent manner with a weak induction of apoptosis on the tsFT210 cells, while 6 induced mainly apoptosis of the same tsFT210 cells also in a dose-dependent manner together with a weak inhibition of the cell cycle at the G0/G1 and G2/M phases, demonstrating that 1-6 exert their anti-proliferative effect on tsFT210 cells through inhibiting cell cycle and inducing apoptosis. In contrast to the cell cycle G2/M phase inhibitory main effect on tsFT210 cells, 5 induced mainly apoptosis on human myeloid leukemia K562 cells with a weak inhibition of the cell cycle at the G2/M phase. The present result provides flavonoids 1-6 as new cell cycle inhibitors and 1 and 4 as new anticancer flavonoids, which not only provide the first example of cell cycle G2/M phase inhibitory and apoptosis-inducing constituents of V. trifolia L. but also explain the use of Vitex trifolia L. by Chinese people to treat cancers.
机译:六种类黄酮,首次从三叶胶中分离出新的细胞周期抑制剂,分别是persicogenin(1),artemetin(2),木犀草素(3),penduletin(4),vitexicarpin(5)和chrysosplenol-D(6)。 L.是一种通过生物测定指导的分离程序治疗癌症的中药。通过光谱法鉴定它们。已经通过SRB(磺胺丁二胺B)方法评估了1-6对哺乳动物癌细胞的抑制作用,并通过流式细胞术,光学显微镜下的形态学观察和琼脂糖凝胶电泳研究了它们对细胞周期和凋亡的影响。以检测核小体间DNA片段化。化合物1-6抑制小鼠tsFT210癌细胞的增殖,IC50s(microg ml(-1))> 100(100 microg ml(-1)的抑制率,47.9%)1> 100(100%的抑制率) microg ml(-1),占2、10.7,占3、19.8,占4、0.3,占5、3.5和6,占69.6%。流式细胞仪研究1-6显示,1-5主要抑制了G2 / M期以剂量依赖性方式诱导tsFT210细胞凋亡,而6期也以剂量依赖性方式主要诱导同一tsFT210细胞凋亡,并且对G0 / G1细胞周期的抑制作用较弱。和G2 / M期,表明1-6通过抑制细胞周期和诱导细胞凋亡对tsFT210细胞发挥抗增殖作用。与对tsFT210细胞的细胞周期G2 / M期抑制主要作用相反,5主要诱导人骨髓白血病K562细胞凋亡,但对G2 / M期的细胞周期抑制作用较弱。本结果提供了黄酮类化合物1-6作为新的细胞周期抑制剂,以及1和4作为新的抗癌类黄酮,不仅提供了三叶草细胞周期G2 / M期抑制和凋亡诱导成分的第一个实例,而且还提供了解释中国人使用三叶胶(Vitex trifolia L.)治疗癌症。

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