Guo Yan Hong, Wang Yong, Xin Min
a Department of Physiology , Guilin Medical University , Guilin , China.
Pharm Biol. 2016 Feb 26:1-6. doi: 10.3109/13880209.2015.1129546.
Context Formononetin is a typical phytoestrogen, which is a bioactive component found in red clover plants. Previous studies have shown that formononetin inhibits the proliferation of several types of cancer cells, including prostate cancer and osteosarcoma. However, how formononetin affects the proliferation of CNE2 is not clear. Objective The objective of this study is to investigate the effects of formononetin on nasopharyngeal carcinoma cells in vitro, along with the underlying mechanism. Materials and methods CNE2 cells were incubated with various concentrations of formononetin (0, 0.1, 0.2, 0.3 and 1 μM) for 48 h. Cell proliferation was measured by [3-(4,5-dimethylthiazol-2-yl)]-2,5-diphenyltetrazolium bromide (MTT) assay, while the rate of apoptosis was measured by flow cytometry. Bcl-2 and bax mRNA expression levels were determined by real time polymerase chain reaction (RT-PCR), while p-ERK1/2 and bcl-2 protein expression levels were quantified by Western blotting. Results Formononetin promoted the proliferation of CNE2 cells at low concentrations (0, 0.05, 0.1, 0.2, 0.5, 1, 2 and 5 μM), OD values increased from 0.27 ± 0.01 to 0.30 ± 0.01, 0.30 ± 0.01,0.36 ± 0.01, 0.35 ± 0.01, 0.34 ± 0.01, 0.34 ± 0.01 and 0.32 ± 0.01, respectively. The percentage of late apoptosis declined from 6.77% ± 0.73% (0 μM group) to 6.2% ± 0.4% (0.1 μM group), 3.83% ± 0.71% (0.3 μM group) and 5.1% ± 0.52% (1M group). The mRNA levels of bax and bcl-2 were down- and upregulated, respectively, by formononetin. Bcl-2 and p-ERK1/2 protein levels were also upregulated. Conclusions Formononetin stimulates CNE2 cell proliferation and has an inhibitory effect on CNE2 cells apoptosis, which is mediated by the activation of the ERK1/2 signaling pathways.
背景 芒柄花黄素是一种典型的植物雌激素,是红三叶草植物中发现的一种生物活性成分。先前的研究表明,芒柄花黄素可抑制多种癌细胞的增殖,包括前列腺癌和骨肉瘤。然而,芒柄花黄素如何影响CNE2细胞的增殖尚不清楚。目的 本研究旨在探讨芒柄花黄素对鼻咽癌细胞的体外作用及其潜在机制。材料与方法 将CNE2细胞与不同浓度的芒柄花黄素(0、0.1、0.2、0.3和1 μM)孵育48小时。通过[3-(4,5-二甲基噻唑-2-基)]-2,5-二苯基四氮唑溴盐(MTT)法检测细胞增殖,通过流式细胞术检测凋亡率。通过实时聚合酶链反应(RT-PCR)测定Bcl-2和bax mRNA表达水平,通过蛋白质印迹法定量p-ERK1/2和bcl-2蛋白表达水平。结果 芒柄花黄素在低浓度(0、0.05、0.1、0.2、0.5、1、2和5 μM)下促进CNE2细胞增殖,OD值分别从0.27±0.01增加到0.30±0.01、0.30±0.01、0.36±0.01、0.35±0.01、0.34±0.01、0.34±0.01和0.32±0.01。晚期凋亡百分比从6.77%±0.73%(0 μM组)降至6.2%±0.4%(0.1 μM组)、3.83%±0.71%(0.3 μM组)和5.1%±0.52%(1 μM组)。芒柄花黄素分别下调bax和上调bcl-2的mRNA水平。Bcl-2和p-ERK1/2蛋白水平也上调。结论 芒柄花黄素刺激CNE2细胞增殖并对CNE2细胞凋亡具有抑制作用,这是由ERK1/2信号通路的激活介导的。