国际肿瘤学杂志 ›› 2016, Vol. 43 ›› Issue (6): 401-404.doi: 10.3760/cma.j.issn.1673-422X.2016.06.001

• 论著 •    下一篇

NDRG2基因对结肠癌细胞SW620增殖和侵袭力的影响

王建勋,曾甜,张鹏,王治刚,雷海录   

  1. 710054 西安,解放军第451医院肝胆普外科(王建勋、张鹏、王治刚、雷海录);解放军第323医院麻醉科(曾甜)
  • 收稿日期:2015-11-24 出版日期:2016-06-08 发布日期:2016-04-27
  • 通讯作者: 雷海录 E-mail:leihailu451@163.com

Effects of tumor suppressor NDRG2 gene on proliferation and invasive ability of colon cancer cell line SW620

Wang Jianxun*, Zeng Tian, Zhang Peng, Wang Zhigang, Lei Hailu.   

  1. *Department of Hepatobiliary and General Surgery, the 451th Hospital of PLA, Xi′an 710054, China
  • Received:2015-11-24 Online:2016-06-08 Published:2016-04-27
  • Contact: Lei Hailu E-mail:leihailu451@163.com

摘要: 目的 观察N-myc下游调节基因2(NDRG2)对结肠癌细胞SW620生长和侵袭能力的影响,并探讨其机制。方法 采用阳离子脂质体转染方法,分别将pcDNA3.1NDRG2和siRNANDRG2转染入SW620细胞内,以空白组作为对照。Western blotting检测各组细胞NDRG2以及基质金属蛋白酶-2(MMP-2)的表达情况;细胞侵袭试验对各组细胞侵袭能力进行分析;四甲基偶氮唑蓝法对各组细胞生长曲线进行测定。结果  pcDNA3.1NDRG2转染入SW620细胞后,NDRG2蛋白表达升高,而MMP-2蛋白表达降低;siRNANDRG2转染入SW620细胞后,NDRG2蛋白表达降低,而MMP2蛋白表达升高。pcDNA3.1组的穿膜细胞数(56.20±7.40)及siRNA组穿膜细胞数(94.20±9.23)分别与对照组(75.80±4.82)相比,差异具有统计学意义(t=13.102,P=0.000;t=11.820,P=0.000)。生长曲线显示,转染后第5天,pcDNA3.1组细胞吸光度值(0.46±0.01)及siRNA组细胞吸光度值(0.91±0.02)分别与对照组(0.67±0.01)相比,差异具有统计学意义(t=9.561,P=0.000;t=10.922,P=0.000)。结论NDRG2能降低结肠癌细胞SW620的侵袭和增殖能力,其机制可能与下调MMP-2的表达有关。

关键词: 结肠肿瘤, 印迹法, 蛋白质, 转染, NDRG2基因

Abstract: Objective  To observe the influence of N-myc downstreamregulated gene 2 (NDRG2) on the growth and invasive ability of human colon cancer cell line SW620, and to explore its mechanism. MethodspcDNA3.1NDRG2 and siRNANDRG2 were transfected transiently respectively into SW620 by Lipofectamine TM 2000, untreated cells as the control group. Western blotting was used to investigate the expression of NDRG2 and matrix metalloproteinase-2(MMP-2). Matrigel invasion assay was used to study the invasive abilities of SW620 cells in all groups. The growth curve was determined through 3(4,5dimethyl2thiazoly)2,5diphenyl2Htetrazolium bromide method. ResultAfter transfecting pcDNA3.1NDRG2 into the SW620 cells, the protein level of NDRG2 increased and the expression of MMP-2 declined markedly. After transfecting siRNANDRG2 into the SW620 cells, the protein level of NDRG2 declined and the expression of MMP2 increased markedly. In addition, compared with the control group (75.80 ±4.82), the numbers of transmembrane cells in pcDNA3.1 group (56.20 ±7.40) and in siRNA group (94.20 ±9.23) were significantly different (t=13.102, P=0.000; t=11.820, P=0.000). The growth curve showed that: compared with the control group (0.67±0.01), the absorbance of the fifth day after transfection in pcDNA3.1 group (0.46±0.01) and in siRNA group (0.91±0.02) were different significantly (t=9.561, P=0.000; t=10.922, P=0.000). ConclusionNDRG2 can reduce the invasion and proliferation ability of colon cancer cell SW620, and its mechanism may be related to the downregulation of MMP-2 expression.

Key words: Colonic neoplasms, Blotting, Western, Transfection, NDRG2 gene