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作 者:刘芬[1] 何艳[1] 李云森[1] 朱永明[2] 刘海燕[1]
机构地区:[1]苏州大学生物医学研究院肿瘤细胞与分子免疫实验室,江苏苏州215123 [2]苏州大学医学部药学院,江苏苏州215123
出 处:《现代肿瘤医学》2011年第12期2393-2396,共4页Journal of Modern Oncology
基 金:苏州市重点实验室资助项目(编号:SWG0904;SS201032)
摘 要:目的:探讨lupeol及其结构改造后衍生/修饰物对肝癌细胞HepG2和SMMC7721细胞增殖的作用。方法:对lupeol进行化学结构修饰,然后应用MTT方法检测lupeol及其衍生/修饰物对HepG2和SMMC7721细胞增殖的作用。结果:MTT数据显示,lupeol及其衍生/修饰物均能抑制HepG2和SMMC7721细胞增殖,并且具有浓度依赖性。Lupeol、H1、T1和T2的IC50分别为40μmol/L-50μmol/L、约120μmol/L、约50μmol/L和70μmol/L-80μmol/L。结论:lupeol结构改造后,并没有提高其对肝细胞肝癌细胞增殖的抑制作用。Objective:To investigate the effects of lupeol and its modified compounds on proliferation of hepatocellular carcinoma cells HepG2 and SMMC7721.Methods: The structure of lupeol was modified.Then cell viability of HepG2 and SMMC7721 was measured by MTT assay after treatment with increasing concentration of lupeol or its modified compounds.Results: MTT results showed that lupeol and its modified compounds inhibited the proliferation of HepG2 and SMMC7721 cells in a concentration dependent manner.IC50 of lupeol,H1,T1 and T2 were 40 μmol/L-50 μmol/L,about 120 μmol/L,about 50 μmol/L and 70 μmol/L-80 μmol/L,respectively.Conclusion: Modification of lupeol performed in the current study did not improve its therapeutic effects in hepatocellular carcinoma.
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