首页> 美国卫生研究院文献>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
【2h】

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基酯衍生物诱导头颈部鳞状上皮癌细胞(底特律562)的细胞周期阻滞和凋亡反应

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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 μM (CA) and 83.25 μM (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 μM and 100 μM doses. The rise of mainly late apoptosis was observed for 100 μM 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特性。研究了生物活性酚类化合物,咖啡酸(CA)及其衍生物咖啡酸苯乙酯(CAPE)的凋亡潜力对人头颈部鳞状细胞癌(HNSCC)(底特律562)细胞增殖和凋亡的影响并进行比较。通过流式细胞术分析癌细胞的凋亡率和细胞周期停滞。发现暴露于CA和CAPE导致底特律562细胞在不同水平下的存活率呈剂量依赖性降低。 CA / CAPE处理确实显着影响了底特律562细胞的生存能力(MTT结果)。 CAPE介导的活力丧失发生在较低剂量下,并且更为明显,其浓度可将细胞生长抑制50%的浓度估计为201.43μM(CA)和83.25μM(CAPE)。带有膜联蛋白V标记的死细胞分析表明,CA和CAPE处理的底特律562细胞在50μm和100μm剂量下均能诱导凋亡。 100μM剂量观察到主要是晚期凋亡的增加,CA / CAPE处理确实影响了G0 / G1期细胞的分布。不同酚类化合物(可能与化学治疗剂)的组合可以被视为抗癌药。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号