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首页> 外文期刊>Journal of International Dental and Medical Research >Apoptosis Induction (Caspase-3,-9) and Human Tongue Squamous Cell Carcinoma VEGF Angiogenesis Inhibition using Flavonoid’s Ethyl Acetate Fraction of Papua Ant Hill (Myrmecodia pendans) SP-C1
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Apoptosis Induction (Caspase-3,-9) and Human Tongue Squamous Cell Carcinoma VEGF Angiogenesis Inhibition using Flavonoid’s Ethyl Acetate Fraction of Papua Ant Hill (Myrmecodia pendans) SP-C1

机译:巴布亚蚁丘(Myrmecodia pendans)SP-C1的类黄酮乙酸乙酯部分抑制细胞凋亡诱导(Caspase-3,-9)和人舌鳞状细胞癌VEGF血管生成。

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摘要

Human tongue squamous cell carcinoma was casued by inability to control cell survival and to control cel motility. Apoptosis is a normal component process of multicellular organism’s development and health. Apoptosis is a programmed cell death as a response to various stimuli. Angiogenesis or neovascularisation is a basic developing sign in cell physiology and pathology. This research was to identify flavonoid’s ethyl acetate fraction from Anthill (Myrmecodia pendans) which has a potential as a anti-cancer to SP-C1 cell. This research was to analyze the Anthill flavonoid’s ethyle acetate as an anti cancer to apoptosis induction (caspase-3 and -9 analyses) to Supri’s Clone (SP-C1) tongue cancer cell and to analyze angiogenesis inhibition by VEGF protein expression. The data from this research was analyzed using Two Way ANOVA and t test (Tukey’s test) with confidence interval 95%. Caspase-3 and -9 colorimetric analyses showed increasing SP-C1 cell inhibition by time and concentration. ELISA analysis showed increasing proteolytic activity on caspase-9 compared with caspase-3. Increasing proteolytic activity with the increasing concentration from 5 μg/ml to 100 μg/ml could also be observed. VEGF angiogenesis inhibition showed increased flavonoid concentration was followed by increased VEGF expression. Otherwise, SP-C1 cell (control) did not show any VEGF expression. Anthill’s flavonoid ethyl acetate fraction (Myrmecodia pendans) had anti-tumor activity on several molecular targets from apoptosis and VEGF angiogenesis of tongue squamous cell carcinoma.
机译:人舌鳞状细胞癌是由于无法控制细胞存活和控制细胞运动而引起的。凋亡是多细胞生物发展与健康的正常过程。凋亡是程序性细胞死亡,是对各种刺激的反应。血管生成或新血管形成是细胞生理学和病理学的基本发展迹象。这项研究旨在从Anthill(Myrmecodia pendans)中鉴定出类黄酮的乙酸乙酯级分,该级分可能对SP-C1细胞具有抗癌作用。这项研究旨在分析蚁丘黄酮的乙酸乙酯作为抗Supri's克隆(SP-C1)舌癌细胞凋亡诱导(caspase-3和-9分析)的抗癌药物,并分析VEGF蛋白表达对血管生成的抑制作用。使用双向方差分析和t检验(Tukey检验)分析了这项研究的数据,置信区间为95%。 Caspase-3和-9比色分析显示,SP-C1细胞的抑制作用随时间和浓度而增加。 ELISA分析显示,与caspase-3相比,其对caspase-9的蛋白水解活性增强。还可以观察到蛋白水解活性随浓度从5μg/ ml增加到100μg/ ml而增加。 VEGF血管生成抑制作用表明,类黄酮浓度增加,其次是VEGF表达增加。否则,SP-C1细胞(对照)未显示任何VEGF表达。 Anthill的类黄酮乙酸乙酯馏分(Myrmecodia pendans)对舌鳞状细胞癌的凋亡和VEGF血管生成的几个分子靶标具有抗肿瘤活性。

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