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黄芪多糖抑制人乳腺癌MCF-7细胞增殖和诱导凋亡 被引量:10

Proliferation inhibition and apoptosis induction ofAstragalus polysaccharides in human breast cancer MCF-7 cells
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摘要 目的探讨中药黄芪多糖的体外抗人乳腺癌MCF.7细胞活性。方法实验分为空白对照组、黄芪多糖组和阳性对照组,黄芪多糖组MCF.7细胞给予不同浓度(2.5、5、10、20mg/L)的黄芪多糖,阳性对照组给予10gmol/L顺铂,空白对照组给予等体积培养基。48h后应用四甲基偶氮唑蓝(MTT)法测黄芪多糖对MCF-7细胞增殖抑制率,计算IC_50;吖啶橙(AO),溴化乙啶(EB)荧光染色法测定黄芪多糖对MCF-7细胞诱导凋亡作用;应用流式细胞仪分析黄芪多糖对MCF-7细胞凋亡和细胞周期的影响。结果在给予2.5、5、10、20mg/L黄芪多糖48h后,黄芪多糖呈浓度依赖性抑制MCF.7细胞的增殖(r=0.985,P〈0.05),抑制率分别为(4.14±2.96)%、(7.14±2.10)%、(20.13±2.33)%、(64.66±5.15)%,高于空白对照组0%,但4个不同浓度组的抑制率均低于阳性对照组(90.31±4.92)%。黄芪多糖48h的IC_50=16.83mg/L。随着黄芪多糖浓度的逐渐增高,MCF-7细胞中代表凋亡的玛瑙色逐渐增多,细胞核骤缩、核分裂,细胞形态呈现典型的凋亡特征。2.5、5、10、20mg/L黄芪多糖的凋亡率分别为(2.37±0.98)%、(6.76±1.31)%、(11.65±1.46)%、(20.75±2.68)%,高于空白对照组(1.14±1.25)%(均P〈0.05),但均低于阳性对照组(35.09±2.88)%(均P〈0.05)。与空白对照组比较,黄芪多糖以浓度依赖性诱导MCF-7细胞凋亡(r=0.991,P〈0.05),随浓度的增加,细胞凋亡率升高,但均低于阳性对照组。黄芪多糖随浓度的增加促使s期细胞比例逐渐升高,但低于空白和阳性对照组(均P〈0.05),使处于G_0-G_1期细胞的比例逐渐减少,仍高于空白和阳性对照组(均P〈0.05)。结论黄芪多糖抑制人乳腺癌MCF-7细胞增殖并诱导其凋亡,使MCF-7细胞生长增殖停滞在S期� Objective To explore the in vitro anti-breast cancer activity of a traditional Chinese medicine, Astragalus polysaccharides (APS), in MCF-7 ceils. Methods The MCF-7 cells were divided into three groups: treated with different concentrations of APS (2.5, 5, 10 and 20 mg/L) (APS group), with 10 μmol]L cisplastin (positive control group) , with equivalent volume of media(blank control group). After 48 h, methylthiazolyl tetrazolium (MTT)test was used to evaluate the proliferation inhibition and then the IC_50 was calculated; acridine orange (AO)-ethidium bromide (EB) fluorescence staining was used to evaluate the induced apoptosis of MCF-7 cells; ftow cytometry was used to analyze the apoptosis and cell cycle. Results After 48 h treatment, different concentrations of APS (2.5, 5, 10 and 20 mg/L) were shown to inhibit the proliferation of MCF-7 cells in a dose-dependent manner (r=0.985, P〈0.05) , with the rates of inhibition being (4.14±2.96)%, (7.14±2.10)%, (20.13±2.33)% and (64.66±5.15)%, respectively. These inhibitionrates were significantly higher than that in blank control group (0%), but lower than that in positive control group (90.31±4.92)%. The IC_50 of APS at 48 h was 16.83 mg/L. Along with higher concentrations of APS, the MCF- 7 cells showed more apoptosis as reflected by an increase in brown- stained cells and typical morphology of apoptosis such as karyopyknosis. The rates of apoptosis by APS were (2.37±0.98)%, (6.76±1.31)%, (I1.65±1.46)%, (20.75±2.68)%, respectively, according different levels(2.5, 5, 10 and 20 mg/ L). These rates were higher than that in blank control group (1.14± 1.25 )%, but lower than that in positive control group (35.09±2.88) % (all P〈0.05). Compared with blank control group, APS induced apoptosis of MCF-7 cells in a dose-dependent manner (r=0.991, P〈0.05). The rates of apoptosis increased with higher doses of APS, but were all lower than that in the positive co
出处 《中华生物医学工程杂志》 CAS 2014年第2期106-109,共4页 Chinese Journal of Biomedical Engineering
基金 国家自然科学基金(81172503)
关键词 黄芪多糖 乳腺肿瘤 细胞增殖 细胞凋亡 Astragalan Breast neoplasms Cell proliferation Apoptosis
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