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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Silver nanoparticles Clinacanthus Nutans leaves extract induced apoptosis towards oral squamous cell carcinoma cell lines
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Silver nanoparticles Clinacanthus Nutans leaves extract induced apoptosis towards oral squamous cell carcinoma cell lines

机译:纳米银Clinacanthus Nutans叶片提取物诱导口腔鳞癌细胞凋亡

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摘要

Purpose: The purpose of this study was to investigate apoptotic activity of silver nanoparticle Clinacanthus nutans (AgNps-CN) towards HSC-4 cell lines (oral squamous cell carcinoma cell lines). Methods: Methods involved were MTT assay (cytotoxic activity), morphological cells analysis, flow cytometry and cell cycle analysis and western blot. Results: MTT assay revealed IC50 concentration was 1.61?μg/mL, 3T3-L1 cell lines were used to determine whether AgNps-CN is cytotoxic to normal cells. At the highest concentration (3?μg/mL), no cytotoxic activity has been observed. Flow cytometry assay revealed AgNps-CN caused apoptosis effects towards HSC-4 cell lines with significant changes were observed at G1 phase when compared with untreated cells. Morphological cells analysis revealed that most of the cells exhibit apoptosis characteristics rather than necrosis. Protein study revealed that ratio of Bax/Bcl-2 increased mainly due to down-regulation of Bcl-2 expression. Conclusion: AgNps-CN have shown potential in inhibiting HSC-4 cell lines. IC50 was low compared to few studies involving biosynthesized of silver nanoparticles. Apoptosis effects were shown towards HSC-4 cell lines by the increased in Bax/Bcl-2 protein ratio. Further study such as PCR or in vivo studies are required.
机译:目的:这项研究的目的是研究银纳米颗粒的藜麦(AgNps-CN)对HSC-4细胞系(口腔鳞状细胞癌细胞系)的凋亡活性。方法:涉及的方法是MTT测定(细胞毒性活性),形态细胞分析,流式细胞仪和细胞周期分析以及蛋白质印迹。结果:MTT法检测IC50浓度为1.61μg/ mL,用3T3-L1细胞株检测AgNps-CN对正常细胞是否有细胞毒性。在最高浓度(3μg/ mL)下,未观察到细胞毒活性。流式细胞仪检测显示,AgNps-CN对HSC-4细胞系具有凋亡作用,与未处理细胞相比,在G1期观察到显着变化。形态细胞分析表明,大多数细胞表现出凋亡特征而不是坏死。蛋白质研究表明,Bax / Bcl-2的比例增加主要是由于Bcl-2表达的下调。结论:AgNps-CN具有抑制HSC-4细胞系的潜力。与少数涉及生物合成银纳米颗粒的研究相比,IC50较低。 Bax / Bcl-2蛋白比率的增加显示出对HSC-4细胞系的凋亡作用。需要进一步的研究,例如PCR或体内研究。

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