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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Induction of Cell Cycle Arrest and Apoptotic Response of Head and Neck Squamous Carcinoma Cells (Detroit 562) by Caffeic Acid and Caffeic Acid Phenethyl Ester Derivative
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Induction of Cell Cycle Arrest and Apoptotic Response of Head and Neck Squamous Carcinoma Cells (Detroit 562) by Caffeic Acid and Caffeic Acid Phenethyl Ester Derivative

机译:咖啡酸和咖啡酸苯乙烷酯衍生物诱导头部和颈部鳞状癌细胞(底特律562)的细胞周期停滞与凋亡响应

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摘要

Natural polyphenols have been observed to possess antiproliferative properties. The effects, including apoptotic potential of bioactive phenolic compounds, caffeic acid (CA) and its derivative caffeic acid phenethyl ester (CAPE), on cell proliferation and apoptosis in human head and neck squamous carcinoma cells (HNSCC) line (Detroit 562) were investigated and compared. Cancer cells apoptosis rates and cell cycle arrests were analysed by flow cytometry. Exposure to CA and CAPE was found to result in a dose-dependent decrease in the viability of Detroit 562 cells at different levels. CA/CAPE treatment did significantly affect the viability of Detroit 562 cells (MTT results). CAPE-mediated loss of viability occurred at lower doses and was more pronounced, with the concentrations which inhibit the growth of cells by 50% estimated at 201.43 muM (CA) and 83.25 muM. (CAPE). Dead Cell Assay with Annexin V labelling demonstrated that CA and CAPE treatment of Detroit 562 cells resulted in an induction of apoptosis at 50 muM and 100 muM doses. The rise of mainly late apoptosis was observed for 100 muM dose and CA/CAPE treatment did affect the distribution of cells in G0/G1 phase. A combination of different phenolic compounds, potentially with chemotherapeutics, could be considered as an anticancer drug.
机译:已经观察到天然多酚具有抗增殖性质。研究了人头和颈部鳞状癌细胞(HNSCC)线(底特律562)的细胞增殖和凋亡的生物活性酚类化合物,咖啡酸(CA)及其衍生物咖啡酸苯乙烷酯(CAPE)的凋亡潜力。并比较。通过流式细胞术分析癌细胞凋亡率和细胞周期滞留。发现暴露于Ca和Cape,导致底特律562个细胞在不同水平的可行性下降的剂量依赖性降低。 Ca / Cape治疗确实显着影响底特律562个细胞的可行性(MTT结果)。侧介导的活力损失在较低剂量下发生,并且更明显,浓度抑制细胞生长的浓度为201.43妈妈(CA)和83.25米估计。 (岬)。具有膜蛋白V标记的死细胞测定证明了底特律562个细胞的Ca和Cape治疗导致50毫米和100毫米剂量的细胞凋亡。为100毫米剂量和Ca / Cape治疗中观察到主要晚期细胞凋亡的兴起确实影响了G0 / G1相中细胞的分布。不同酚类化合物的组合可能与化学治疗剂,可被认为是抗癌药物。

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