中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2010年
8期
1104-1106
,共3页
冯智毅%李伟明%黄波%胡世雄
馮智毅%李偉明%黃波%鬍世雄
풍지의%리위명%황파%호세웅
胰腺癌%金属硫蛋白1E%Cyclin D1%p53
胰腺癌%金屬硫蛋白1E%Cyclin D1%p53
이선암%금속류단백1E%Cyclin D1%p53
Pancreatic carcinoma%MT1E%Cyclin Dl%p53
目的 观察外源性人金属硫蛋白1E(MT1E)基因对胰腺癌SW1990细胞生长的影响.方法 构建MT1E基因真核表达载体,转染SW1990细胞并获得阳性单克隆细胞.用Westernblot技术检测转染前后MT1E蛋白表达,噻唑蓝(MTT)实验检测其增殖能力的变化,流式细胞仪分析细胞周期时相分布.同时检测Cyclin D1与p53的表达.结果 MT1E融合蛋白在SW1990MT1E细胞中表达.MTT结果表明,与SW1990和SW1990MT1E空细胞比较,SW1990MT1E细胞增殖速度明显增快.SW1990MT1E细胞与SW1990和SW1990空细胞比较,G0/G1期细胞明显减少,S期明显增多,差异有统计学意义.SW1990MT1E较SW1990空的细胞Cyclin D1与p53表达明显升高.结论 MT1E能够促进SW1990增殖,可能和上调Cyclin D1促使细胞进入S期增多,通过失活p53蛋白使细胞恶性变.
目的 觀察外源性人金屬硫蛋白1E(MT1E)基因對胰腺癌SW1990細胞生長的影響.方法 構建MT1E基因真覈錶達載體,轉染SW1990細胞併穫得暘性單剋隆細胞.用Westernblot技術檢測轉染前後MT1E蛋白錶達,噻唑藍(MTT)實驗檢測其增殖能力的變化,流式細胞儀分析細胞週期時相分佈.同時檢測Cyclin D1與p53的錶達.結果 MT1E融閤蛋白在SW1990MT1E細胞中錶達.MTT結果錶明,與SW1990和SW1990MT1E空細胞比較,SW1990MT1E細胞增殖速度明顯增快.SW1990MT1E細胞與SW1990和SW1990空細胞比較,G0/G1期細胞明顯減少,S期明顯增多,差異有統計學意義.SW1990MT1E較SW1990空的細胞Cyclin D1與p53錶達明顯升高.結論 MT1E能夠促進SW1990增殖,可能和上調Cyclin D1促使細胞進入S期增多,通過失活p53蛋白使細胞噁性變.
목적 관찰외원성인금속류단백1E(MT1E)기인대이선암SW1990세포생장적영향.방법 구건MT1E기인진핵표체재체,전염SW1990세포병획득양성단극륭세포.용Westernblot기술검측전염전후MT1E단백표체,새서람(MTT)실험검측기증식능력적변화,류식세포의분석세포주기시상분포.동시검측Cyclin D1여p53적표체.결과 MT1E융합단백재SW1990MT1E세포중표체.MTT결과표명,여SW1990화SW1990MT1E공세포비교,SW1990MT1E세포증식속도명현증쾌.SW1990MT1E세포여SW1990화SW1990공세포비교,G0/G1기세포명현감소,S기명현증다,차이유통계학의의.SW1990MT1E교SW1990공적세포Cyclin D1여p53표체명현승고.결론 MT1E능구촉진SW1990증식,가능화상조Cyclin D1촉사세포진입S기증다,통과실활p53단백사세포악성변.
Objective To investigate the effects of MT1E gene on the cell proliferation in human pancreatic carcinoma cell line SW1990.Methods Human pancreatic carcinoma cell line SW1990 made by transfection with expressible MT1E gene, Positive monoclone was screened by G418.Western blotting assays were used to identify the expression of MT1E protein respectively. The cell proliferation was determined by MTT assay. The cell cycle was detected by flow cytometry, The apoptosis-related protein levels of Cyclin Dl and p53 determined by immunohistochemistry. Results MT1E protein were expressed in SW1990.Cells tranfected pcDNA3.1 ( - ) -MT1E compared with the SW1990 and cells tranfected pcDNA 3.1 ( - ), proliferation rate significantly enhanced, cells number of G0/G1 phase obviously decreased while cells number of S phase increased, Cyclin Dl and p53 protein levels elevated. Conclusion MT1E could promote proliferation of SW1990 cell by upregulating expression of cyclin Dl and p53 to facilitate cells into S phase.