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蛇葡萄素钠协同卡铂体外诱导肺癌Lewis细胞凋亡研究 被引量:3
Cytotoxic effect of ampelopsin sodium combined with carboplatin on Lewis lung adenocarcinoma cell line
文献类型:期刊文献
中文题名:蛇葡萄素钠协同卡铂体外诱导肺癌Lewis细胞凋亡研究
英文题名:Cytotoxic effect of ampelopsin sodium combined with carboplatin on Lewis lung adenocarcinoma cell line
作者:缪苗苗[1,2];吴勇杰[2];覃红[2];张艳霞[2,3]
第一作者:缪苗苗
机构:[1]兰州市第二人民医院,甘肃兰州730046;[2]兰州大学基础医学院药理学研究所,甘肃省新药临床前研究重点实验室,甘肃兰州730000;[3]甘肃中医药大学,甘肃兰州730000
第一机构:兰州市第二人民医院,甘肃兰州730046
年份:2016
卷号:21
期号:11
起止页码:1271
中文期刊名:中国临床药理学与治疗学
外文期刊名:Chinese Journal of Clinical Pharmacology and Therapeutics
收录:CSTPCD;;CSCD:【CSCD2015_2016】;
语种:中文
中文关键词:蛇葡萄素钠;卡铂;肺癌Lewis细胞;细胞凋亡
外文关键词:ampelopsin sodium ; carboplatin ;mouse Lewis lung cancer cells; apoptosis
摘要:目的:考察蛇葡萄素钠(AMP-Na)单用及与卡铂合用对肺癌Lewis细胞增殖的抑制作用,初步探讨AMP-Na抑瘤作用机制。方法:应用MTT法考察AMP-Na单用及与卡铂合用对肺癌Lewis细胞的细胞毒作用;使用流式细胞仪检测凋亡相关基因Bax以及Bcl-2表达。结果:体外细胞毒实验结果表明,AMP-Na在12.5~200.0μg/m L的浓度范围内对肺癌Lewis细胞的增殖具有浓度依赖性的抑制作用,其IC_(50)为63.1μg/m L;6.3、12.5、25.0、50.0μg/m L的AMP-Na与卡铂3.1~25.0μg/m L联合用药对卡铂抑制Lewis细胞的增殖作用具有协同效应;流式细胞仪检测结果显示,AMP-Na 12.5、25.0、50.0、100.0μg/m L单用及与卡铂25.0μg/m L联合应用处理细胞48h后,Bax的表达升高,Bcl-2的表达降低(P〈0.01),Bcl-2/Bax比率降低。结论:蛇葡萄素钠单用对Lewis细胞的增殖具有一定的抑制作用,与卡铂合用,对Lewis细胞增殖具有协同抑制效应;蛇葡萄素钠可能是通过下调Bcl-2并上调Bax从而促进肿瘤细胞凋亡。
AIM : effect and mechanism To investigate the cytotoxic of ampelopsin sodium ( AMP- Na) alone or combined with carboplatin on Lewis lung cancer cells. METHODS: MTT colorimetric method was used to investigate cytotoxic effect of AMP-Na alone or combined with carboplatin on Lew- is lung cancer cells. Flow cytometry(FCM) was used to analyze the cell apoptosis. RESULTS: Experimental study on cytotoxicity in vitro showed that the proliferation of Lewis lung cancer ceils was inhibited by AMP-Na alone in a concentration-dependent manner ranging from 12. 5-200.0 μg/mL and its IC50 was 63.1 μg/mL. Combined with carboplatin, AMP-Na of 6.3, 12.5,25.0 and 50.0μg/mL had synergistic inhibitory effect on the proliferation of Lewis cells. FCM results showed the ratio of Bcl-2/ Bax was decreased significantly in Lewis cells trea- ted with AMP-Na ( 12.5, 25.0, 50.0, 100.0 μg/ mL) or in combination with earboplatin (25 μg/ mL) for 48 hours. CONCLUSION : AMP-Na de- creases Lewis cells survival rate in a concentration- dependent manner. Combined with carboplatin, AMP-Na has synergistic inhibitory effect on the pro- liferation of Lewis cells. The apoptosis inducing effect is partially mediated by Bcl-2/Bax in Lewis cells treated with AMP-Na alone or in combination with carboplatin.
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