中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2011年
11期
1835-1837
,共3页
金旭红%沈东炎%万云燕%李文岗
金旭紅%瀋東炎%萬雲燕%李文崗
금욱홍%침동염%만운연%리문강
七叶皂苷钠%增殖%胆管癌
七葉皂苷鈉%增殖%膽管癌
칠협조감납%증식%담관암
Sodium aescinate%Proliferation%Cholangiocarcinoma
目的 观察七叶皂苷钠对人胆管癌细胞株Hccc9810增殖和凋亡的影响.方法 运用细胞染色、噻唑蓝(MTT)比色法、流式细胞术和实时荧光定量聚合酶链反应(PCR)等技术观察不同浓度(0、10、20、40 μmol/L)七叶皂苷钠对胆管癌细胞增殖、细胞周期和凋亡的影响.结果 七叶皂苷钠呈时间剂量依赖性抑制胆管癌细胞Hccc9810的增殖,其24、48、72 h的50%抑制浓度(IC50)分别为:(45.34±2.12)、(33.00±1.92)、(25.00±1.65) μmol/L;G1期比例从(49.49±1.22)%上升到(70.20±1.52)%;胆管癌细胞形态发生典型凋亡特征性改变,凋亡率随浓度的升高从20.54%上升到62.56%,差异均有统计学意义(P<0.05).结论 七叶皂苷钠通过阻滞细胞周期和诱导细胞凋亡而抑制胆管癌细胞Hccc9810增殖.
目的 觀察七葉皂苷鈉對人膽管癌細胞株Hccc9810增殖和凋亡的影響.方法 運用細胞染色、噻唑藍(MTT)比色法、流式細胞術和實時熒光定量聚閤酶鏈反應(PCR)等技術觀察不同濃度(0、10、20、40 μmol/L)七葉皂苷鈉對膽管癌細胞增殖、細胞週期和凋亡的影響.結果 七葉皂苷鈉呈時間劑量依賴性抑製膽管癌細胞Hccc9810的增殖,其24、48、72 h的50%抑製濃度(IC50)分彆為:(45.34±2.12)、(33.00±1.92)、(25.00±1.65) μmol/L;G1期比例從(49.49±1.22)%上升到(70.20±1.52)%;膽管癌細胞形態髮生典型凋亡特徵性改變,凋亡率隨濃度的升高從20.54%上升到62.56%,差異均有統計學意義(P<0.05).結論 七葉皂苷鈉通過阻滯細胞週期和誘導細胞凋亡而抑製膽管癌細胞Hccc9810增殖.
목적 관찰칠협조감납대인담관암세포주Hccc9810증식화조망적영향.방법 운용세포염색、새서람(MTT)비색법、류식세포술화실시형광정량취합매련반응(PCR)등기술관찰불동농도(0、10、20、40 μmol/L)칠협조감납대담관암세포증식、세포주기화조망적영향.결과 칠협조감납정시간제량의뢰성억제담관암세포Hccc9810적증식,기24、48、72 h적50%억제농도(IC50)분별위:(45.34±2.12)、(33.00±1.92)、(25.00±1.65) μmol/L;G1기비례종(49.49±1.22)%상승도(70.20±1.52)%;담관암세포형태발생전형조망특정성개변,조망솔수농도적승고종20.54%상승도62.56%,차이균유통계학의의(P<0.05).결론 칠협조감납통과조체세포주기화유도세포조망이억제담관암세포Hccc9810증식.
Objective To investigate the effects of sodium aescinate on the proliferation and apoptosis of cholangiocarcinoma Hccc9810 cell line.Methods The effects of sodium aescinate (0,10,20,40μmol/L) on cell growth,cycle and apoptosis were investigated by methyl thiazol tetrazolium (MTT) assay,flow cytometry,and fluorescence microscopy.Results Sodium aescinate inhibited cholangiocarcinoma cell growth in a dose- and time-dependent manner,and its half-inhibitory concentration (IC50) for 24 h,48 h,and 72 h was (45.34 ±2.12),(33.00± 1.92) and (25.00 ± 1.65) μmol/L respectively.The proportion of cells in G1 phase was increased from (49.49 ± 1.22)% to (70.20 ± 1.52)%.The apoptosis rote was increased from 20.54% to 62.56% (P <0.05).Conclusion Sodium aescinate exhibited its anticarcinoma effect probably through regulating cell cycle and inducing cell apoptosis.