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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Anticancer activity of a novel glycoprotein from Camellia oleifera Abel seeds against hepatic carcinoma in vitro and in vivo
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Anticancer activity of a novel glycoprotein from Camellia oleifera Abel seeds against hepatic carcinoma in vitro and in vivo

机译:来自山茶花Oleifera的新型糖蛋白的抗癌活性在体外和体内肝癌中的肝癌反对肝癌

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摘要

Glycoproteins are naturally occurring biological macromolecule that possess known pharmacological properties. This study investigated the anticancer potential of a new glycoprotein, COG2a with the weight-average molecular weight of 25.9 kDa, isolated from Camellia oleifera Abel seeds by multiple column chromatography and the mechanism of anticancer action. MIT assay showed that the maximum inhibition rate of COG2a on HepG2 cells was 92.1%. Electron microscopic and fluorescence microscopy observation indicated that the HepG2 cells treated with COG2a exhibited typical apoptotic morphological character. Flow cytometry manifested that COG2a induced the cell cycle arrest at the G2 phases and decreased in mitochondrial membrane potential on the HepG2 cells. Western blotting exhibited that COG2a increased the expressions of the pro-apoptotic protein caspase-3 and Bax and decreased the expression of the anti-apoptotic proteins Bcl-2. Additionally, COG2a exerted an obvious anticancer effect on tumor-bearing mice and the maximum tumor inhibition rate is 72.77%. It also can promote the mouse thymus and pancreas index, the number of T lymphocytes cell subset and interferon-gamma to increase. These results indicate that COG2a exhibits in vitro and in vivo anticancer activities that associate with its immunopotentiation properties and may serve as a potential anticancer agent. (C) 2019 Elsevier B.V. All rights reserved.
机译:糖蛋白是天然存在的生物大分子,具有已知的药理学性质。本研究研究了新糖蛋白的抗癌潜力Cog2a,其重量平均分子量为25.9kDa,通过多柱色谱法和抗癌作用的机制分离出山茶花油籽。麻省理工学院检测表明,HepG2细胞上的CoG2a的最大抑制率为92.1%。电子显微镜和荧光显微镜观察表明,用COG2A处理的HEPG2细胞表现出典型的凋亡形态特性。流式细胞术表明,COG2A在G2阶段诱导细胞周期停滞,并在HepG2细胞上降低线粒体膜电位。蛋白质印迹表明Cog2a增加了促凋亡蛋白质caspase-3和Bax的表达,并降低了抗凋亡蛋白Bcl-2的表达。此外,COG2A对携带肿瘤小鼠的显而易见的抗癌效果,最大肿瘤抑制率为72.77%。它还可以促进小鼠胸腺和胰腺指数,T淋巴细胞细胞群的数量和干扰素 - γ增加。这些结果表明Cog2a在体外和体内抗癌活动中展示,与其免疫抑制性能相关,并可作为潜在的抗癌剂。 (c)2019 Elsevier B.v.保留所有权利。

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