中国癌症杂志 ›› 2015, Vol. 25 ›› Issue (9): 659-664.doi: 10.3969/j.issn.1007-3969.2015.09.003

• 论著 • 上一篇    下一篇

miR-1284过表达对人胃癌SGC-7901细胞基因表达谱及侵袭转移的影响

韦尉元1,蓸稳珑1,詹泽栩1,余 晗1,谢玉波2,肖 强1   

  1. 1. 广西医科大学第一附属医院胃肠腺体外科,广西 南宁530021 ;
    2. 广西医科大学第一附属医院麻醉科,广西 南宁530021
  • 出版日期:2015-09-30 发布日期:2015-12-15
  • 通信作者: 肖强 E-mail:xiaoqiang20050@aliyun.com
  • 基金资助:
    广西科学技术攻关项目(桂科攻14124004-1-9);2015年广西研究生教育创新计划项目(YCBZ2015028)。

The effect of miR-1284 over-expression on gene expression profiling and invasion/metastasis of human gastric cancer SGC-7901 cells

WEI Weiyuan1, CAO Wenlong1, ZHAN Zexu1, YU Han1, XIE Yubo2, XIAO Qiang1   

  1. 1. Department of Gastrointestine and Gland Surgery, First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi, China; 2. Department of Anesthesiology, First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi, China
  • Published:2015-09-30 Online:2015-12-15
  • Contact: XIAO Qiang E-mail: xiaoqiang20050@aliyun.com

摘要: 背景与目的:人胃癌组织微小RNA表达谱芯片筛选研究报道miR-1284与胃癌淋巴结转移有关,但其在胃癌中的具体作用鲜见报道。该研究探讨miR-1284过表达对人胃癌SGC-7901细胞基因表达谱及侵袭转移的影响。方法:以慢病毒介导miR-1284过表达转染胃癌SGC-7901细胞为实验组(LV-miR-1284组),转染空载体慢病毒载体的细胞为阴性对照组(LV-NC-GFP组),未转染慢病毒载体的细胞为空白组(Control组)。采用荧光定量PCR检测各组细胞miR-1284的表达,芯片检测各组细胞差异表达基因,生物信息学预测miR-1284的靶基因,Transwell侵袭实验检测各组细胞侵袭能力,裸鼠皮下移植瘤模型检测各组细胞转移能力。结果:PCR结果显示,与LV-NC-GFP组和Control组比较,LV-miR-1284组细胞miR-1284表达明显增高;芯片结果显示,LV-miR-1284组有20个基因表达显著上调,17个基因表达显著下调;生物信息学预测miR-1284的靶基因有138个基因;Transwell侵袭实验结果显示,LV-miR-1284组侵袭细胞数为70.00±2.37,其细胞侵袭能力较LV-NCGFP组(168.67±4.55)和Control组(170.33±3.08)明显减弱;体内裸鼠实验结果显示,LV-miR-1284组肝脏转移率为14.29%,其细胞转移能力较LV-NC-GFP组(85.71%)和Control组(85.71%)明显减弱。结论:miR-1284过表达能抑制人胃癌SGC-7901细胞侵袭转移,其机制可能与调控SUMO1JUN基因表达有关。

关键词: 胃癌, miR-1284, 侵袭, 转移

Abstract: Background and purpose: It has been reported that miR-1284 is associated with gastric cancer lymph node metastasis in the research of microRNA microarray in human gastric cancer tissues. But the specific role of miR-1284 in gastric cancer has not been reported. The aim of this study was to investigate the effect of miR-1284 over-expression on the gene expression profiling and invasion/metastasis of human gastric cancer SGC-7901 cells. Methods: Gastric cancer SGC-7901 cells of LV-miR-1284 group were transfected with lentiviral vectors of miR-1284, cells of LV-NC-GFP group were transfected with lentiviral vectors without miR-1284, and cells of control group were not transfected with lentiviral vectors. The expression of miR-1284 was detected by the real-time fluorescent quantitative PCR. Differential expression genes were detected by the microRNA chip. Target genes of miR-1284 were predicted by the bioinformatics. Invasive ability was detected by the Transwell invasion assay. Metastasis ability was detected by subcutaneously transplanted tumor model of nude mice. Results: Compared with LV-NC-GFP and control groups, the expressions of miR-1284 and 20 genes were up-regulated, and the expression of 17 genes was down-regulated in LV-miR-1284 group. One hundred and thirty-eight target genes of miR-1284 were predicted by the bioinformatics website. Compared with invasive cell number of LV-NC-GFP group (168.67±4.55) and control group  170.33±3.08), the ability of invasion of cells was weakened in LV-miR-1284 group (70.00±2.37). Compared with the liver metastasis rate of LV-NC-GFP group (85.71%) and control group (85.71%), the ability of metastasis of cells was weakened in LV-miR-1284 group (14.29%). Conclusion: The ability of invasion and metastasis of SGC-7901 cells is suppressed by over-expression of miR-1284. The mechanism may be related to regulating the expression of SUMO1 and JUN genes.

Key words: Gastric carcinoma, miR-1284, Invasion, Metastasis