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五倍子酸对小鼠胃癌MFC和肝癌H22细胞增殖的抑制作用
引用本文:王丽萍,曾宪旭,牛凤兰,石卓.五倍子酸对小鼠胃癌MFC和肝癌H22细胞增殖的抑制作用[J].郑州大学学报(医学版),2012,47(3):339-341.
作者姓名:王丽萍  曾宪旭  牛凤兰  石卓
作者单位:王丽萍 (郑州大学基础医学院组织学与胚胎学教研室,郑州,450001) ; 曾宪旭 (吉林大学基础医学院药理学教研室,长春,130021) ; 牛凤兰 (郑州大学第三附属医院病理科,郑州,450052) ; 石卓 (吉林大学公共卫生学院卫生毒理学教研室,长春,130021) ;
摘    要:目的:研究五倍子酸(GA)对小鼠胃癌MFC细胞及小鼠肝癌H22细胞增殖的影响。方法:分别用3.125、6.250、12.500、25.000、50.000和100.000mg/L的GA处理MFC和H22细胞48h后,应用MTT法检测细胞的增殖抑制率;分别以6.25、12.50和25.00mg/L的GA作用MFC和H22细胞48h后,应用流式细胞仪检测细胞周期及凋亡情况;建立移植性H22和MFC荷瘤小鼠模型,分别给予0.50、0.25和0.20g/kgGA、环磷酰和生理盐水10d后计算抑瘤率。结果:GA呈剂量依赖性抑制MFC及H22细胞增殖(F=70.845、145.444,P<0.001)。GA使MFC细胞和H22细胞均阻滞在G0/G1期(F=80.432、42.903,P<0.001),各组MFC细胞凋亡率差异有统计学意义(F=45.831,P<0.001)。不同剂量GA对荷MFC和H22瘤小鼠的抑瘤率差异有统计学意义(F=206.264、110.906,P<0.001)。结论:GA具有较好的抑制MFC和H22细胞增殖的作用。

关 键 词:五倍子酸  MFC细胞  H22细胞  小鼠  增殖

Inhibitive effects of gallic acid on proliferation of murine gastric cancer and hepatoma-22 cells
WANG Liping,ZENG Xianxu,NIU Fenglan,SHI Zhuo.Inhibitive effects of gallic acid on proliferation of murine gastric cancer and hepatoma-22 cells[J].Journal of Zhengzhou University: Med Sci,2012,47(3):339-341.
Authors:WANG Liping  ZENG Xianxu  NIU Fenglan  SHI Zhuo
Institution:1)Department of Histology and Embryology,College of Basic Medical Sciences,Zhengzhou University,Zhengzhou 450001 2)Department of Pharmacology,College of Basic Medical Sciences,Jilin University,Changchun 130021 3)Department of Pathology,the Third Affiliated Hospital,Zhengzhou University,Zhengzhou 450052 4)Department of Hygienic Toxicology,School of Public Health,Jilin University,Changchun 130021
Abstract:Aim:To explore the effect of gallic acid(GA) on proliferation of murine gastric cancer(MFC) and hepatoma-22(H22) cells.Methods:MTT was employed to detect proliferation ability of MFC and H22 cells treated with 3.125,6.250,12.500,25.000,50.000 and 100.000 mg/L GA for 48 h,respectively.Flow cytometry was used to examine cell cycle progression and apoptotic rate of MFC and H22 cells treated with 6.25,12.50 and 25.00 mg/L GA for 48 h.Tumor inhibition rates were calculated after the mice bearing H22 or MFC cells,which were administered GA(0.50,0.25 and 0.20 g/kg),cyclophosphamide or normal saline for 10 days.Results:The proliferation inhibtion rate of GA on MFC and H22 cells were enhanced in a dose-dependant manner(F=70.845,145.444;P<0.001).Both MFC and H22 cells were arrested at G0/G1(F=80.432,42.903;P<0.001) and increase of cellular apoptosis was detected in MFC cells(F=45.831,P<0.001).The anti-tumor rates of the different dosage of GA for mice bearing MFC and H22 cells had significant differences(F=206.264,110.906;P<0.001).Conclusion:GA is applicable to inhibit proliferation of MFC and H22 cells both in vivo and in vitro mainly.
Keywords:gallic acid  MFC cell  H22 cell  mouse  proliferation
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