首页> 美国卫生研究院文献>Saudi Journal of Biological Sciences >Plant derived coumestrol phytochemical targets human skin carcinoma cells by inducing mitochondrial-mediated apoptosis cell cycle arrest inhibition of cell migration and invasion and modulation of m-TOR/PI3K/AKT signalling pathway
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Plant derived coumestrol phytochemical targets human skin carcinoma cells by inducing mitochondrial-mediated apoptosis cell cycle arrest inhibition of cell migration and invasion and modulation of m-TOR/PI3K/AKT signalling pathway

机译:植物衍生的CoMeStrol植物化学靶向人体皮肤癌细胞通过诱导线粒体介导的细胞凋亡细胞周期停滞抑制细胞迁移和侵袭和调节M-TOR / PI3K / AKT信号通路

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摘要

The current study was undertaken to investigate anticancer activity of coumestrol phytoestrogen against human skin cancer. MTT assay was performed for cell viability assessment and clonogenic assay for cell colony formation assessment. Apoptosis was analysed by Annexin V/FITC staining, AO/EB staining and western blotting assays. Effects on the m-TOR/PI3K/AKT signalling pathway were investigated by western blotting. Results indicated that coumestrol induced significant toxicity in human skin cancer cells in contrast to mouse skin cancer cells. The proliferation rate in normal skin cells remained almost intact. Annexin V-FITC and AO/EB staining assays indicated coumestrol induced cytotoxicity in skin cancer cells is mediated through apoptosis stimulation. The apoptosis in skin cancer cells was mediated through caspase-activation. Cell migration and invasion was inhibited by coumestrol in human skin cancer cells via inhibition of MMP-2 and MMP-9 expressions. Moreover, m-TOR/PI3K/AKT signalling pathway in SKEM-5 cells was blocked by coumestrol.
机译:本研究旨在调查CoMeStro植物雌激素对人体皮肤癌的抗癌活性。对细胞残留性评估和用于细胞菌落形成评估进行的细胞活力评估和克隆核来进行MTT测定。通过膜蛋白V / FITC染色,AO / EB染色和蛋白质印迹测定分析细胞凋亡。通过蛋白质印迹研究了对M-TOR / PI3K / AKT信号通路的影响。结果表明,与小鼠皮肤癌细胞相比,Coumestro诱导人体皮肤癌细胞中的显着毒性。正常皮肤细胞中的增殖速率几乎完好无损。膜蛋白V-FITC和AO / EB染色测定表明Coumestrol诱导皮肤癌细胞中的细胞毒性通过凋亡刺激介导。皮肤癌细胞中的凋亡通过Caspase-as活化介导。通过抑制MMP-2和MMP-9表达,COMERROL在人体皮肤癌细胞中抑制细胞迁移和侵袭。此外,SKEM-5细胞中的M-TOR / PI3K / AKT信号传导途径被COMERROL阻止。

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