首页> 外文期刊>International Journal of Clinical and Experimental Medicine >Globularifolin exhibits potentanticancer activity on A549 human lungcancer cell line via induction of mitochondrialapoptosis, cell cycle arrest and NF-kB inhibition
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Globularifolin exhibits potentanticancer activity on A549 human lungcancer cell line via induction of mitochondrialapoptosis, cell cycle arrest and NF-kB inhibition

机译:Globularifolin通过诱导线粒体凋亡,细胞周期阻滞和NF-kB抑制作用,对A549人肺癌细胞显示出有效的抗癌活性。

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Globularifolin is an iridoid glucoside and has only been isolated from some plant species of plantaginaceae.Iridoids glucosides have been reported to exhibit tremendous pharmacological potential. However, the anticanceractivity of the rare acylated iridoid glucoside globularifolin has not been reported so far. In the present studywe determined its anticancer potential against human lung cancer A549 cancer cell line. The results showed thatglobularifolin has an IC50 value of 12.5 μM human lung cancer cells and inhibited the colony formation potential ina dose-dependent manner. The molecule exerted its anticancer activity through induction of apoptosis by regulatingBcl-2/Bax signaling pathway. Additionally, it caused cell cycle arrest of human lung cancer A549 cancer cells atG2/M phase. Globularifolin was also found to cause reduction in the mitochondrial membrane potential in a dosedependent manner. Additionally, globularifolin effectively inhibited NF-kB almost by 50% at 25 μM concentrationat 24 h incubation. We conclude that globularifolin exerts its anticancer activity through induction of mitochondrialapoptosis, G2/M cycle arrest and NF-kB inhibition indicating it may prove as a lead molecule treatment of lungcancer.
机译:Globularifolin是一种鸢尾糖苷,仅从一些植物科植物中分离出来。据报道,鸢尾糖苷具有巨大的药理潜力。然而,到目前为止,尚未报道过稀有的酰化的虹彩化合物糖苷球蛋白的抗癌活性。在本研究中,我们确定了其对人肺癌A549癌细胞系的抗癌潜力。结果表明,球状氟哌啶醇具有12.5μM的人肺癌细胞IC50值,并以剂量​​依赖性方式抑制集落形成潜能。该分子通过调节Bcl-2 / Bax信号通路诱导细胞凋亡发挥其抗癌活性。另外,它引起人肺癌A549癌细胞在G2 / M期的细胞周期停滞。还发现globularifolin以剂量依赖的方式引起线粒体膜电位的降低。此外,在24 h孵育25μM浓度时,球状富林有效抑制NF-kB达50%。我们得出的结论是,球状ifolin通过诱导线粒体凋亡,G2 / M周期阻滞和NF-kB抑制发挥其抗癌活性,表明它可能被证明是治疗肺癌的先导分子。

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