维生素C对AS_2O_3抑制肺癌A549细胞增殖、诱导细胞凋亡作用的影响及机制  被引量:9

Effect of Vitamin C on the arsenic trioxide roles of inhibiting the proliferation and inducing the apoptosis in lung carcinoma cell lines A549 and its mechanism

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作  者:曾锦荣[1] 谭宁[1] 翟鹏勇[1] 王绩英[2] 佘巍巍 

机构地区:[1]桂林医学院附属医院,广西桂林541001 [2]桂林医学院生物技术学院

出  处:《山东医药》2010年第3期7-9,共3页Shandong Medical Journal

基  金:广西壮族自治区自然科学基金资助项目(2009AM9087);广西壮族自治区卫生厅立项课题资助项目(Z2007226)

摘  要:目的探讨维生素C对三氧化二砷(AS2O3)抗癌作用的影响及其可能机制。方法将体外培养的肺腺癌A549细胞随机分为6组,其中对照组不行特殊处理,AS2O3 1—3组分别加入0.4、4.0、40μg/ml的AS2O3,维生素C组加入400μg/ml的维生素C,联合组加入400μg/ml维生素C+0.4μg/ml AS2O3。采用缩胆囊素八肽(CCK-8)法及克隆形成实验检测细胞生长情况(A值),用流式细胞仪检测细胞周期及凋亡率,用RT-PCR方法检测Caspase-3 mRNA、多药耐药相关蛋白基因1(MRP1)mRNA、多药耐药基因1(MDR1)mRNA表达情况(维生素C组)。结果联合组及AS2O3 2、3组A值均显著低于对照组及AS:O3组、维生素C组,且随作用时间延长逐渐降低(P〈0.05);联合组细胞集落显著少于其他五组,G0/G1期所占比例及凋亡率均显著高于其他五组(P〈0.05);维生素C组Caspase-3 mRNA、MDR1 mRNA表达升高(P〈0.05)、MRP1 mRNA表达无明显变化(P〉0.05)。结论维生素C对As2O3抗肺腺癌A549细胞的作用具有协同性,可能机制为上调Caspase-3表达;两者联用可望成为低毒高效的化疗组合。Objective To investigate the effect of Vitamin C on the anti-cancer roles of arsenic trioxide (AS2O3 ) and the possible mechanism. Methods A549 cells cultured in vitro were divided into 6 groups randomly. The control gruop was given no especial treatment, and AS2O3 1-3 group were treated with AS2O3 at the concentration of 0.4,4.0,40 μg/ml, the Vitamin C gruop was treated with Vitamin C of 400 μg/ml,the combined group was treated with Vitamin C of 400 μg/ml + 0.40 μg/ml AS203-The cell proliferation (A value)was measured by CCK-8 assay and clonogcntic assay, the ceil cycle and apoptosis were detected by flow cytometry, the expressions of Caspase-3 mRNA, MRPI mRNA, MDR1 mRNA were measured by RT-PCR assay(Vitamin C group). Results The absorbance of the combined group and AS2O3 2-3 groups were significantly lower than that of the AS2O3 1 group and Vitamin C group,which decreased gradually with the time extension (P 〈 0.05). The ceil colony of the combined group was significantly fewer than that of the other groups, while the percentage of Go/Gt and apoptosis were significantly higher( P 〈 0.05 ). The expression of Caspase-3 mRNA and MDR1 mRNA of the Vitamin C group increased(P 〈 0.05 ) ,the expression of MRP1 mRNA showed no significant changes( P 〉 0.05 ). Conclusion Vitamin C has synergistic action on the antilung adenocarcinoma roles of AS2O3 , possible mechanism is related to the up-ragulation of the expression of Caspase-3 mRNA. Application of Vitamin C and AS2O3 might be a chemotherapy combination with low toxicity and efficient.

关 键 词:三氧化二砷 维生素C 肺肿瘤 肺癌 细胞凋亡 多药耐药基因1 多药耐药相关蛋白基因1 

分 类 号:R734.2[医药卫生—肿瘤] R949.1[医药卫生—临床医学]

 

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