南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2013年
10期
1494-1498
,共5页
杜潇%张思琴%程中%李旸%王自强%陈志新%胡建昆%周总光
杜瀟%張思琴%程中%李旸%王自彊%陳誌新%鬍建昆%週總光
두소%장사금%정중%리양%왕자강%진지신%호건곤%주총광
胰腺癌%Notch信号通路%Notch胞内段%增殖%凋亡
胰腺癌%Notch信號通路%Notch胞內段%增殖%凋亡
이선암%Notch신호통로%Notch포내단%증식%조망
pancreatic cancer%Notch signaling pathway%Notch intracellular domain%proliferation%apoptosis
目的探讨转染人Notch1受体胞内段(NICD)质粒激活Notch1信号通路对胰腺癌细胞增殖的影响及其可能机制。方法构建带免疫荧光的NICD质粒与对照质粒,细胞转染后荧光激发显微镜下观察转染效率,Real-time PCR检测靶基因Hes1表达水平变化;CCK-8法计算NICD质粒转染后胰腺癌细胞增殖的影响;caspase 3试剂盒检测NICD转染后凋亡通路关键酶caspase 3活性的变化。结果荧光激发显示NICD转染效率在60%~80%之间;NICD转染可促进靶基因Hes1表达,提示激活Notch1信号通路。NICD转染可显著促进胰腺癌细胞生长增殖;caspase 3活性在NICD转染后明显下降,差异均具有统计学意义。结论应用NICD质粒转染激活Notch1信号通路活性可通过抑制凋亡而促进胰腺癌细胞生长增殖。
目的探討轉染人Notch1受體胞內段(NICD)質粒激活Notch1信號通路對胰腺癌細胞增殖的影響及其可能機製。方法構建帶免疫熒光的NICD質粒與對照質粒,細胞轉染後熒光激髮顯微鏡下觀察轉染效率,Real-time PCR檢測靶基因Hes1錶達水平變化;CCK-8法計算NICD質粒轉染後胰腺癌細胞增殖的影響;caspase 3試劑盒檢測NICD轉染後凋亡通路關鍵酶caspase 3活性的變化。結果熒光激髮顯示NICD轉染效率在60%~80%之間;NICD轉染可促進靶基因Hes1錶達,提示激活Notch1信號通路。NICD轉染可顯著促進胰腺癌細胞生長增殖;caspase 3活性在NICD轉染後明顯下降,差異均具有統計學意義。結論應用NICD質粒轉染激活Notch1信號通路活性可通過抑製凋亡而促進胰腺癌細胞生長增殖。
목적탐토전염인Notch1수체포내단(NICD)질립격활Notch1신호통로대이선암세포증식적영향급기가능궤제。방법구건대면역형광적NICD질립여대조질립,세포전염후형광격발현미경하관찰전염효솔,Real-time PCR검측파기인Hes1표체수평변화;CCK-8법계산NICD질립전염후이선암세포증식적영향;caspase 3시제합검측NICD전염후조망통로관건매caspase 3활성적변화。결과형광격발현시NICD전염효솔재60%~80%지간;NICD전염가촉진파기인Hes1표체,제시격활Notch1신호통로。NICD전염가현저촉진이선암세포생장증식;caspase 3활성재NICD전염후명현하강,차이균구유통계학의의。결론응용NICD질립전염격활Notch1신호통로활성가통과억제조망이촉진이선암세포생장증식。
Objective To observe the effect of activation of Notch1 signaling pathway by Notch intracellular domain (NICD) plasmid transfection on pancreatic cancer cell proliferation and explore the underlying mechanism. Methods The transfection rates were observed under microscope with fluorescence stimulation, and mRNA expression levels of Hes1 were detected by real-time PCR. Cell proliferation changes were evaluated by CCK-8 after NICD and control plasmid transfection in pancreatic cancer cells. Caspase 3 activity was examined using a caspase 3 detection kit. Results The transfection rates of NICD plasmid were up to 80% by fluorescence stimulation observation. Hes1 expression was significantly increased after NICD plasmid transfection, suggesting the activation of Notch1 signaling pathway. NICD plasmid transfection significantly promoted cancer cell proliferation compared to control plasmid transfeciton. The activities of caspase 3 were obviously decreased after NICD plasmid transfection in 3 pancreatic cancer cell lines. Conclusions Activation of Notch1 signaling pathway by NICD plasmid transfection can promote the proliferation of pancreatic cancer cells by inhibiting the apoptosis pathway.