Faraji Seyed Nooredin, Mojtahedi Zahra, Ghalamfarsa Ghasem, Takhshid Mohammad Ali
Diagnostic Laboratory Sciences and Technology Research Center, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
Shiraz Institute for Cancer Research, School of Medicine, Shiraz University of Medical sciences, Shiraz, Iran.
Iran J Basic Med Sci. 2015 Aug;18(8):773-9.
N-myc downstream regulated gene 2 (NDRG2) is a candidate gene for tumor suppression. The expression of NDRG2 is down-regulated in several tumors including lung cancer. The aim of this study was to explore the effect of NDRG2 overexpression on invasion, migration, and enzymatic activity of matrix metalloproteinase-2 (MMP-2) and -9 (MMP-9) in human lung adenocarcinoma A549 cells.
A recombinant plasmid encoding green fluorescent protein (GFP)-tagged NDRG2 (pCMV6-AC-NDRG2-GFP) was used to overexpress GFP-tagged NDRG2 in A549 cells. The cells in the experimental group and those in the control group were transfected with pCMV6-AC-NDRG2-GFP and a control plasmid without NDRG2 (pCMV6-AC-GFP), respectively. Fluorescent microscopy and flowcytometry analysis of GFP expression were used to evaluate the cellular expression of GFP-tagged NDRG2 and the efficiency of transfection. The effects of NDRG2 expression on cell invasion and migration were evaluated using transwell filter migration assay. The gelatinase activity of secreted MMP-2 and MMP-9 was measured by gelatin zymography.
Our results demonstrated the expression of GFP-tagged NDRG2 in the cytoplasm and nucleus of A549 cells. The findings of transwell assay showed that NDRG2 overexpression reduced migration and invasion of A549 cells compared to control cells. Gelatin zymography analyses revealed that NDRG2 overexpression decreased the gelatinase activity of secreted MMP-2 and MMP-9.
These findings suggest that NDRG2 may be a new anti-invasion factor in lung cancer that inhibits MMPs activities.
N-myc下游调控基因2(NDRG2)是一种肿瘤抑制候选基因。NDRG2的表达在包括肺癌在内的多种肿瘤中下调。本研究旨在探讨NDRG2过表达对人肺腺癌A549细胞侵袭、迁移以及基质金属蛋白酶-2(MMP-2)和-9(MMP-9)酶活性的影响。
使用编码绿色荧光蛋白(GFP)标记的NDRG2的重组质粒(pCMV6-AC-NDRG2-GFP)在A549细胞中过表达GFP标记的NDRG2。实验组细胞和对照组细胞分别用pCMV6-AC-NDRG2-GFP和不含NDRG2的对照质粒(pCMV6-AC-GFP)转染。通过GFP表达的荧光显微镜和流式细胞术分析来评估GFP标记的NDRG2的细胞表达和转染效率。使用Transwell滤膜迁移试验评估NDRG2表达对细胞侵袭和迁移的影响。通过明胶酶谱法测量分泌的MMP-2和MMP-9的明胶酶活性。
我们的结果证明了GFP标记的NDRG2在A549细胞的细胞质和细胞核中的表达。Transwell试验结果表明,与对照细胞相比,NDRG2过表达降低了A549细胞的迁移和侵袭。明胶酶谱分析显示,NDRG2过表达降低了分泌的MMP-2和MMP-9的明胶酶活性。
这些发现表明,NDRG2可能是肺癌中一种新的抗侵袭因子,可抑制基质金属蛋白酶的活性。