生物技术通讯
生物技術通訊
생물기술통신
LETTERS IN BIOTECHNOLOGY
2013年
4期
519-522
,共4页
乔志新%贺敏%李伟静%任素萍%王春燕%苏丽华%王璇琳%于群
喬誌新%賀敏%李偉靜%任素萍%王春燕%囌麗華%王璇琳%于群
교지신%하민%리위정%임소평%왕춘연%소려화%왕선림%우군
胰腺癌细胞%雷公藤甲素%细胞凋亡
胰腺癌細胞%雷公籐甲素%細胞凋亡
이선암세포%뢰공등갑소%세포조망
pancreatic cancer cells%triptolide%apoptosis
目的:观察雷公藤甲素对胰腺癌细胞BxPC-3和PANC-1生长抑制及诱导细胞凋亡作用,探讨雷公藤甲素抗胰腺癌的机制。方法:雷公藤甲素处理BxPC-3和PANC-1细胞后,用MTT法检测细胞的生长抑制,用流式细胞术检测细胞的凋亡率,用罗丹明123和DCFH-DA染色方法测定细胞线粒体膜跨膜电位变化和活性氧(ROS)的产生,用Western印迹检测Bcl-2、Bax蛋白表达的变化。结果:雷公藤甲素对胰腺癌细胞BxPC-3和PANC-1具有生长抑制和诱导细胞凋亡的作用,且呈时间和剂量依赖关系;处理72 h后,胰腺癌细胞线粒体跨膜电位明显下降,Bax表达上调, Bcl-2表达下降。结论:雷公藤甲素能有效抑制胰腺癌细胞增殖,通过增强线粒体通透性诱导细胞凋亡。
目的:觀察雷公籐甲素對胰腺癌細胞BxPC-3和PANC-1生長抑製及誘導細胞凋亡作用,探討雷公籐甲素抗胰腺癌的機製。方法:雷公籐甲素處理BxPC-3和PANC-1細胞後,用MTT法檢測細胞的生長抑製,用流式細胞術檢測細胞的凋亡率,用囉丹明123和DCFH-DA染色方法測定細胞線粒體膜跨膜電位變化和活性氧(ROS)的產生,用Western印跡檢測Bcl-2、Bax蛋白錶達的變化。結果:雷公籐甲素對胰腺癌細胞BxPC-3和PANC-1具有生長抑製和誘導細胞凋亡的作用,且呈時間和劑量依賴關繫;處理72 h後,胰腺癌細胞線粒體跨膜電位明顯下降,Bax錶達上調, Bcl-2錶達下降。結論:雷公籐甲素能有效抑製胰腺癌細胞增殖,通過增彊線粒體通透性誘導細胞凋亡。
목적:관찰뢰공등갑소대이선암세포BxPC-3화PANC-1생장억제급유도세포조망작용,탐토뢰공등갑소항이선암적궤제。방법:뢰공등갑소처리BxPC-3화PANC-1세포후,용MTT법검측세포적생장억제,용류식세포술검측세포적조망솔,용라단명123화DCFH-DA염색방법측정세포선립체막과막전위변화화활성양(ROS)적산생,용Western인적검측Bcl-2、Bax단백표체적변화。결과:뢰공등갑소대이선암세포BxPC-3화PANC-1구유생장억제화유도세포조망적작용,차정시간화제량의뢰관계;처리72 h후,이선암세포선립체과막전위명현하강,Bax표체상조, Bcl-2표체하강。결론:뢰공등갑소능유효억제이선암세포증식,통과증강선립체통투성유도세포조망。
Objective: To determine whether triptolide inhibits proliferation and induces apoptosis of pancreatic cancer cells. Methods: The effects of triptolide on the antiproliferative activity of pancreatic cancer cells BxPC-3 and PANC-1 were determined by MTT assays. Apoptosis of pancreatic cancer cells induced by triptolide were de-termined by flow cytometry analysis. Mitochondrial membranere potential and ROS production analysis were detect-ed by Rhodamine 123 and DCFH-DA. The effects of triptolide on expression levels of Bcl-2 and Bax were deter-mined by Western blotting. Results: Triptolide displayed inhibition activity of cells growth and induction of apopto-sis on pancreatic cancer cells. Triptolide induced the loss of mitochondrial membrane potential by regulating the expression levels of Bcl-2 family proteins. Conclusion: The results suggest that triptolide may inhibit proliferation and induce apoptosis of pancreatic cancer cells by inducing the loss of mitochondrial membrane potential.