贵州医药
貴州醫藥
귀주의약
GUIZHOU MEDICAL JOURNAL
2014年
6期
506-508
,共3页
李晋%徐尚福%殷国海%徐亚沙%谭州科
李晉%徐尚福%慇國海%徐亞沙%譚州科
리진%서상복%은국해%서아사%담주과
红枣多糖%肝癌HepG2 细胞%细胞周期%凋亡
紅棘多糖%肝癌HepG2 細胞%細胞週期%凋亡
홍조다당%간암HepG2 세포%세포주기%조망
Red datas polysaccharide%HePG2%Cell cycle%Apoptosis
目的:研究红枣多糖对体外培养肝癌细胞增殖的抑制作用并初步探究其可能的作用机理。方法采用M T T法测定红枣多糖对体外培养的人肝癌细胞HepG2增殖的抑制作用;流式细胞术检测红枣多糖对人肝癌细胞HepG2周期和凋亡的影响;Real time RT-PCR检测红枣多糖对人肝癌细胞HepG2中Bcl-2和caspase3 mRNA表达的影响。结果 MTT检测发现随着药物浓度的增高OD值呈现梯度递减,红枣多糖对 HepG2的IC50=13 mg/mL ,最高浓度40 mg/mL下所得最大抑制率为68.79%;流式细胞仪检测细胞凋亡结果可见早期凋亡率随药物浓度的增加而变大;流式细胞周期分析结果可见G0-G1期细胞数逐渐增多,S期细胞数有下降趋势,并有剂量依赖性;Real time RT-PCR检测发现Bcl-2凋亡抑制基因mRNA表达随药物浓度增高而降低,而凋亡关键基因caspase-3 mRNA的表达随药物浓度增高而升高。结论红枣多糖对体外培养的肝癌细胞增值具有抑制作用,将肝癌细胞HepG2阻滞于G1期,并通过下调Bc 1-2而上调caspase-3 mRNA表达诱导 HepG2细胞凋亡。
目的:研究紅棘多糖對體外培養肝癌細胞增殖的抑製作用併初步探究其可能的作用機理。方法採用M T T法測定紅棘多糖對體外培養的人肝癌細胞HepG2增殖的抑製作用;流式細胞術檢測紅棘多糖對人肝癌細胞HepG2週期和凋亡的影響;Real time RT-PCR檢測紅棘多糖對人肝癌細胞HepG2中Bcl-2和caspase3 mRNA錶達的影響。結果 MTT檢測髮現隨著藥物濃度的增高OD值呈現梯度遞減,紅棘多糖對 HepG2的IC50=13 mg/mL ,最高濃度40 mg/mL下所得最大抑製率為68.79%;流式細胞儀檢測細胞凋亡結果可見早期凋亡率隨藥物濃度的增加而變大;流式細胞週期分析結果可見G0-G1期細胞數逐漸增多,S期細胞數有下降趨勢,併有劑量依賴性;Real time RT-PCR檢測髮現Bcl-2凋亡抑製基因mRNA錶達隨藥物濃度增高而降低,而凋亡關鍵基因caspase-3 mRNA的錶達隨藥物濃度增高而升高。結論紅棘多糖對體外培養的肝癌細胞增值具有抑製作用,將肝癌細胞HepG2阻滯于G1期,併通過下調Bc 1-2而上調caspase-3 mRNA錶達誘導 HepG2細胞凋亡。
목적:연구홍조다당대체외배양간암세포증식적억제작용병초보탐구기가능적작용궤리。방법채용M T T법측정홍조다당대체외배양적인간암세포HepG2증식적억제작용;류식세포술검측홍조다당대인간암세포HepG2주기화조망적영향;Real time RT-PCR검측홍조다당대인간암세포HepG2중Bcl-2화caspase3 mRNA표체적영향。결과 MTT검측발현수착약물농도적증고OD치정현제도체감,홍조다당대 HepG2적IC50=13 mg/mL ,최고농도40 mg/mL하소득최대억제솔위68.79%;류식세포의검측세포조망결과가견조기조망솔수약물농도적증가이변대;류식세포주기분석결과가견G0-G1기세포수축점증다,S기세포수유하강추세,병유제량의뢰성;Real time RT-PCR검측발현Bcl-2조망억제기인mRNA표체수약물농도증고이강저,이조망관건기인caspase-3 mRNA적표체수약물농도증고이승고。결론홍조다당대체외배양적간암세포증치구유억제작용,장간암세포HepG2조체우G1기,병통과하조Bc 1-2이상조caspase-3 mRNA표체유도 HepG2세포조망。
Objective To study the multiplication effect of red dates polysaccharide on tumor cells in vitro and preliminarily explored its possible mechanism .Methods MTT method was used to determi-nate the value-added effect on human hepatoma cells HepG2 in vitro .Used the flow cytometric to de-tect the effect on human hepatocellular carcinoma cell cycle and apoptosis of red dates polysaccharide in HepG2 .Caspase3 and Bcl-2 mRNA were detected the effect on the expression in HepG2 cells by Real time RT-PCR .Results With the increased concentration of drug ,the OD decreased by the detection of MTT .The inhibition rate of IC50 (13 mg/mL) was 71 .52% .The detection of flow cytometric on ap-optotic cells showed early apoptosis rate increased as the concentration increased .From the result of cell cycle analysis ,the cell number gradually increased between time G0 and G1 ,and decreased in time S as the concentration of red datas polysaccharide was increased .The expression of apoptosis inhibi-ting gene Bcl-2 mRNA decreased when the concentration of drug increased from the analysis by Real Time RT-PCR .Conclusion The red dates polysaccharide has inhibition on cultured hepatoma cells and arrests the hepatoma cells HepG2 in phase G1 ,induces the apoptosis of HepG2 ,inhibits the expression of the mRNA Bcl-2 .