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黄芩素对鼻咽癌CNE2细胞增殖和凋亡的影响
引用本文:余展鹏,宋方茗,蔡琰,孟盈,黄夏宁,黄元姣.黄芩素对鼻咽癌CNE2细胞增殖和凋亡的影响[J].中草药,2018,49(4):879-884.
作者姓名:余展鹏  宋方茗  蔡琰  孟盈  黄夏宁  黄元姣
作者单位:广西医科大学 生物化学与分子生物学教研室, 广西 南宁 530021,广西医科大学 再生医学研究中心, 广西 南宁 530021,广西医科大学 生物化学与分子生物学教研室, 广西 南宁 530021,广西医科大学 生物化学与分子生物学教研室, 广西 南宁 530021,广西医科大学生命科学研究院, 广西 南宁 530021,广西医科大学生命科学研究院, 广西 南宁 530021
基金项目:国家自然科学基金资助项目(81260405);广西自然科学基金项目(2015GXNSFAA139215);广西生物靶向诊治研究重点实验室开放课题(GXSWBX201502)
摘    要:目的研究黄芩素对鼻咽癌CNE2细胞增殖和凋亡的影响,并探讨其阻滞细胞周期和诱导凋亡的机制。方法通过CCK-8法和克隆形成实验检测黄芩素对CNE2细胞增殖的影响,流式细胞仪检测细胞凋亡率和细胞周期变化,荧光显微镜观察细胞形态改变,试剂盒检测Caspase-3蛋白活性变化,实时荧光定量PCR(q RT-PCR)检测P53、P21、CDK2、Caspase-3m RNA表达情况。结果黄芩素对鼻咽癌CNE2细胞增殖具有显著的抑制作用,且呈剂量和时间依赖性,与对照组比较,不同浓度的黄芩素作用于CNE2细胞48 h后,细胞出现典型的凋亡特征,并出现周期阻滞,Caspase-3活性增强,P53及其下游基因P21、Caspase-3 m RNA表达水平增高,CDK2 m RNA表达水平下降。结论黄芩素可抑制鼻咽癌CNE2细胞增殖,可能是通过上调P53表达诱导细胞凋亡并阻滞细胞周期于S期。

关 键 词:黄芩素  鼻咽癌  凋亡  细胞周期  P53
收稿时间:2017/7/21 0:00:00

Effects of baicalein on proliferation and apoptosis of nasopharyngeal carcinoma CNE2 cells
YU Zhan-peng,SONG Fang-ming,CAI Yan,MENG Ying,HUANG Xia-ning and HUANG Yuan-jiao.Effects of baicalein on proliferation and apoptosis of nasopharyngeal carcinoma CNE2 cells[J].Chinese Traditional and Herbal Drugs,2018,49(4):879-884.
Authors:YU Zhan-peng  SONG Fang-ming  CAI Yan  MENG Ying  HUANG Xia-ning and HUANG Yuan-jiao
Institution:Department of Biochemistry and Molecular Biology, Guangxi Medical University, Nanning 530021, China,Research Centre for Regenerative Medicine, Guangxi Medical University, Nanning 530021, China,Department of Biochemistry and Molecular Biology, Guangxi Medical University, Nanning 530021, China,Department of Biochemistry and Molecular Biology, Guangxi Medical University, Nanning 530021, China,Life Sciences Institute, Guangxi Medical University, Nanning 530021, China and Life Sciences Institute, Guangxi Medical University, Nanning 530021, China
Abstract:Objective To investigate the anti-proliferation effect of baicalein in nasopharyngeal carcinoma CNE2 cells and to clarify its mechanisms of cell cycle arrest and apoptosis. Methods The proliferative activity was detected by CCK-8 assay, and the changes of cell morphology was observed under fluorescence microscope. The rate of apoptosis and the cycle arrest were detected by flow cytometry, and caspase-3 activity was detected by caspase-3 activity kit. Expression of related genes (P53, P21, CDK2, and Caspase-3) at the RNA level were detected by using qRT-PCR. Results Baicalein had a significant inhibitory proliferation effect on CNE2 cells, which was the dose and time-dependent. After 48 h treatment with different concentrations of baicalein, the cells showed obvious apoptotic characteristics, with the increase of apoptotic cells, the activity of caspase-3 was increased, and S phase cells increase. Compared with the control group, the mRNA expression of P53, P21 and Caspase-3 increased, and mRNA expression of CDK2 decreased. Conclusion Baicalein could inhibit the proliferation of nasopharyngeal carcinoma CNE2 cells, and may induce apoptosis and cell cycle arrest in S phase by up regulating the expression of P53.
Keywords:baicalein  nasopharyngeal carcinoma  apoptosis  cell cycle  P53
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