华南国防医学杂志
華南國防醫學雜誌
화남국방의학잡지
MILLITARY MEDICAL JOURNAL OF SOUTH CHINA
2001年
2期
1-4
,共4页
聚酯型儿茶素%癌%肝细胞%细胞株
聚酯型兒茶素%癌%肝細胞%細胞株
취지형인다소%암%간세포%세포주
目的:探讨聚酯型儿茶素对人肝癌SMMC-7721细胞的生长抑制作用及其机制。方法:应用MTT法、集落形成试验、同位素掺入试验、细胞内cAMP/cGMP浓度测定、原位杂交等方法进行检测。结果:50mg*L-1聚酯型儿茶素对SMMC-7721细胞的生长、集落形成有明显的抑制作用;3H-TdR、3H-Leu掺入试验证明其可明显抑制细胞DNA和蛋白质合成;聚酯型儿茶素作用后,SMMC-7721细胞内cAMP及cGMP浓度明显增加,细胞的c-myc基因mRNA水平表达明显降低,而p53基因mRNA水平表达明显升高。结论:聚酯型儿茶素对肝癌SMMC-7721细胞的生长有明显的抑制作用,此作用与其抑制细胞DNA和蛋白质合成、升高细胞内cAMP浓度和抑制c-myc基因表达、增强p53基因表达有关。
目的:探討聚酯型兒茶素對人肝癌SMMC-7721細胞的生長抑製作用及其機製。方法:應用MTT法、集落形成試驗、同位素摻入試驗、細胞內cAMP/cGMP濃度測定、原位雜交等方法進行檢測。結果:50mg*L-1聚酯型兒茶素對SMMC-7721細胞的生長、集落形成有明顯的抑製作用;3H-TdR、3H-Leu摻入試驗證明其可明顯抑製細胞DNA和蛋白質閤成;聚酯型兒茶素作用後,SMMC-7721細胞內cAMP及cGMP濃度明顯增加,細胞的c-myc基因mRNA水平錶達明顯降低,而p53基因mRNA水平錶達明顯升高。結論:聚酯型兒茶素對肝癌SMMC-7721細胞的生長有明顯的抑製作用,此作用與其抑製細胞DNA和蛋白質閤成、升高細胞內cAMP濃度和抑製c-myc基因錶達、增彊p53基因錶達有關。
목적:탐토취지형인다소대인간암SMMC-7721세포적생장억제작용급기궤제。방법:응용MTT법、집락형성시험、동위소참입시험、세포내cAMP/cGMP농도측정、원위잡교등방법진행검측。결과:50mg*L-1취지형인다소대SMMC-7721세포적생장、집락형성유명현적억제작용;3H-TdR、3H-Leu참입시험증명기가명현억제세포DNA화단백질합성;취지형인다소작용후,SMMC-7721세포내cAMP급cGMP농도명현증가,세포적c-myc기인mRNA수평표체명현강저,이p53기인mRNA수평표체명현승고。결론:취지형인다소대간암SMMC-7721세포적생장유명현적억제작용,차작용여기억제세포DNA화단백질합성、승고세포내cAMP농도화억제c-myc기인표체、증강p53기인표체유관。
Objective To investigate the inhibitory effect of theasinesin on the growth of SMMC-7721 human hepatic carcinoma cells line and its mechanism. Methods MTT assay, colony formation test,3H-TdR,3H-Leu incorporation test, determination of the intracellular cAMP and cGMP level, in situ hybridization were used. Results Theasinesin at 50mg*L-1 could significantly inhibit the growth and colony formation of SMMC-7721 cells. Theasinesin could strongly inhibit DNA and protein synthesis and increase intracellular cAMP levels. C-myc gene expression was significantly decreased and p53 gene increased strongly in a dose-dependent manner. Conclusions Theasinesin had significant inhibitory effects on the growth of SMMC-7721 cells. Its mechanisms may involve the inhibition of DNA and protein synthesis, the elevation of intracellular cAMP levels, inhibition of c-myc gene expression and enhancement of p53 gene expression.