医学临床研究
醫學臨床研究
의학림상연구
JOURNAL OF CLINICAL RESEARCH
2013年
11期
2209-2212
,共4页
李勇%肖雅玲%陈朝晖%黎明%李青玲%邹欣%周海燕
李勇%肖雅玲%陳朝暉%黎明%李青玲%鄒訢%週海燕
리용%초아령%진조휘%려명%리청령%추흔%주해연
肝肿瘤%姜黄素%巨噬细胞游走抑制因子
肝腫瘤%薑黃素%巨噬細胞遊走抑製因子
간종류%강황소%거서세포유주억제인자
Liver Neoplasms%Curcumin%Macrophage Migration-Inhibitory Factors
[目的]检测人肝癌细胞株HepG2中巨噬细胞迁移抑制因子(MIF)的表达及释放,探讨姜黄素对HepG2中MIF表达的影响。[方法]反转录聚合酶链反应(RT-PCR)及免疫印迹法(Western Blot)检测对照组及不同浓度姜黄素干预组(10,20,30,40,50μmol/L)HepG2中MIF mRNA及蛋白表达水平;ELISA检测对照组及不同浓度姜黄素干预组(10,20,30,40,50μmol/L )培基中 M IF蛋白水平。[结果]HepG2高表达MIF mRNA及MIF蛋白,各浓度姜黄素干预均可抑制HepG2中MIF mRNA及MIF蛋白的表达,且呈浓度依赖效应( P <0.05);HepG2可自分泌MIF蛋白,各浓度姜黄素干预均可抑制 HepG2中MIF 蛋白的释放,且呈浓度依赖效应( P <0.05)。[结论]人肝癌细胞株HepG2可表达及释放MIF ;姜黄素在转录和翻译水平能有效抑制M IF的表达及释放,这可能是其发挥抗肿瘤效应的分子机制之一。
[目的]檢測人肝癌細胞株HepG2中巨噬細胞遷移抑製因子(MIF)的錶達及釋放,探討薑黃素對HepG2中MIF錶達的影響。[方法]反轉錄聚閤酶鏈反應(RT-PCR)及免疫印跡法(Western Blot)檢測對照組及不同濃度薑黃素榦預組(10,20,30,40,50μmol/L)HepG2中MIF mRNA及蛋白錶達水平;ELISA檢測對照組及不同濃度薑黃素榦預組(10,20,30,40,50μmol/L )培基中 M IF蛋白水平。[結果]HepG2高錶達MIF mRNA及MIF蛋白,各濃度薑黃素榦預均可抑製HepG2中MIF mRNA及MIF蛋白的錶達,且呈濃度依賴效應( P <0.05);HepG2可自分泌MIF蛋白,各濃度薑黃素榦預均可抑製 HepG2中MIF 蛋白的釋放,且呈濃度依賴效應( P <0.05)。[結論]人肝癌細胞株HepG2可錶達及釋放MIF ;薑黃素在轉錄和翻譯水平能有效抑製M IF的錶達及釋放,這可能是其髮揮抗腫瘤效應的分子機製之一。
[목적]검측인간암세포주HepG2중거서세포천이억제인자(MIF)적표체급석방,탐토강황소대HepG2중MIF표체적영향。[방법]반전록취합매련반응(RT-PCR)급면역인적법(Western Blot)검측대조조급불동농도강황소간예조(10,20,30,40,50μmol/L)HepG2중MIF mRNA급단백표체수평;ELISA검측대조조급불동농도강황소간예조(10,20,30,40,50μmol/L )배기중 M IF단백수평。[결과]HepG2고표체MIF mRNA급MIF단백,각농도강황소간예균가억제HepG2중MIF mRNA급MIF단백적표체,차정농도의뢰효응( P <0.05);HepG2가자분비MIF단백,각농도강황소간예균가억제 HepG2중MIF 단백적석방,차정농도의뢰효응( P <0.05)。[결론]인간암세포주HepG2가표체급석방MIF ;강황소재전록화번역수평능유효억제M IF적표체급석방,저가능시기발휘항종류효응적분자궤제지일。
[Objective] To detect the expression and releasing of macrophage migration inhibitory factor (MIF) in human hepatocellular carcinoma cell line HepG2 .and to explore the effect of curcumin on the expres-sion of MIF in HepG2 .[Methods] Reverse transcription polymerase chain reaction (RT-PCR) and Western blotting method were used to detect the expression of MIF mRNA and protein in control group and curcumin treatment groups of different concentrations(10 ,20 ,30 ,40 and 50μmol/L) .The expression of MIF protein in control group and curcumin treatment groups of different concentrations (10 ,20 ,30 ,40 and 50μmol/L) was measured by using ELISA .[Results] The expression of MIF mRNA and protein in HepG2 was high .Curcu-min with different concentrations could inhibit the expression of MIF mRNA and protein in HepG 2 in dose-de-pendent manner( P<0 .05) .MIF protein could be released by HepG2 .Curcumin with different concentrations could inhibit the releasing of MIF protein in HepG2 in dose-dependent manner( P<0 .05) .[Conclusion]MIF is expressed in HepG2 and released by HepG2 .Curcumin can effectively inhibit the expression and releasing of MIF at transcription and translation level ,which may be one of the mechanisms of anti-neoplastic effect of cur-cumin .