小G蛋白Ran对胰腺癌细胞增殖和凋亡的调控  

Regulation of Ran GTPase Signaling Pathway on Cell Growth and Apoptosis in Pancreatic Cancer Cells

作　　者：邓林[1] 卢瑗瑗[1] 孙艺[1] 郭学刚[1] 

机构地区：[1]第四军医大学西京消化病院肿瘤生物学国家重点实验室,陕西西安710032

出　　处：《现代生物医学进展》2013年第4期658-661,共4页Progress in Modern Biomedicine

基　　金：国家自然科学基金项目(30971337)

摘　　要：目的:探讨Ras超家族的小G蛋白Ran GTPase在胰腺癌组织及细胞中的表达情况,及其对胰腺癌细胞PANC-1增殖和凋亡的影响。方法:选取胰腺癌石蜡标本及相应正常组织标本各27例进行免疫组织化学染色。用LipofectamineTM2000转染Ran干扰RNA(small interference RNA,siRNA)进入胰腺癌细胞系PANC-1干扰其表达,之后利用Western blot观察Ran的表达情况。运用MTT及流式细胞术分别检测各实验组细胞的增殖和凋亡情况。结果:免疫组化染色显示在胰腺癌组织中Ran的表达阳性率及得分均明显高于癌旁正常组织(P<0.05)。将干扰Ran siRNA转染进入细胞系PANC-1中,利用Western blot发现Ran的表达明显下调。并且通过MTT实验发现在胰腺癌细胞系PANC-1中下调Ran表达能明显抑制该细胞生长(P<0.05),并使PANC-1细胞凋亡显著增多(P<0.05)。结论:小G蛋白Ran GTPase在胰腺癌组织及细胞系中高表达,且Ran可以促进胰腺癌细胞PANC-1的增殖,抑制其凋亡。Objective： To observe the expression of the Ran GTPase in the pancreatic cancer tissues and cells,and the effect of the Ran GTPase on cell growth and apoptosis in PANC-1 pancreatic cancer cells.Methods： A total of 27 paraffin-embedded specimens of primary pancreatic cancer and matched adjacent non-cancerous tissues for Immunohistochemistry.Ran expression was inhibited by small interference RNA,the change of protein level in PANC-1 cell was measured by Western blot.We ues the MTT and flow cytometry（FCM） to detecte the growth rate and apoptosis of PANC-1 cells.Result： The expression level of Ran in pancreatic cancer tissues was sig-nificantly higher than that in matched non-cancerous tissues（P0.05）.After inhibiting Ran expression,the growth of PANC-1 cells was inhibited（P0.05）.However,the apoptosis of PANC-1 cells was increased（P0.05）.Conclusion： Ran was overexpressed in pancreatic cancer tissues compared with non-cancerous tissues,which was determined by immunohistochemical staining.In PANC-1 pancreatic cancer cells,Ran promotes cell growth and inhibits apoptosis.

关 键 词：胰腺癌 RAN GTPASE RNA干扰 细胞增殖 细胞凋亡 

分 类 号：R734.2[医药卫生—肿瘤]