Department of Pathology, The First People's Hospital, Shanghai Jiaotong University, Shanghai, China.
Biochem Biophys Res Commun. 2011 Apr 29;408(1):154-9. doi: 10.1016/j.bbrc.2011.03.140. Epub 2011 Apr 2.
N-myc downstream regulated gene 1 (NDRG1) is an important gene regulating tumor invasion. In this study, shRNA technology was used to suppress NDRG1 expression in CaSki (a cervical cancer cell line) and HO-8910PM (an ovarian cancer cell line). In vitro assays showed that NDRG1 knockdown enhanced tumor cell adhesion, migration and invasion activities without affecting cell proliferation. cDNA microarray analysis revealed 96 deregulated genes with more than 2-fold changes in both cell lines after NDRG1 knockdown. Ten common upregulated genes (LPXN, DDR2, COL6A1, IL6, IL8, FYN, PTP4A3, PAPPA, ETV5 and CYGB) and one common downregulated gene (CLCA2) were considered to enhance tumor cell invasive activity. BisoGenet network analysis indicated that NDRG1 regulated these invasion effector genes/proteins in an indirect manner. Moreover, NDRG1 knockdown also reduced pro-invasion genes expression such as MMP7, TMPRSS4 and CTSK. These results suggest that regulation of invasion and metastasis by NDRG1 is a highly complicated process.
N-myc 下游调节基因 1(NDRG1)是调节肿瘤侵袭的重要基因。本研究采用 shRNA 技术抑制宫颈癌细胞系 CaSki 和卵巢癌细胞系 HO-8910PM 中的 NDRG1 表达。体外实验表明,NDRG1 敲低增强了肿瘤细胞的黏附、迁移和侵袭活性,而不影响细胞增殖。cDNA 微阵列分析显示,NDRG1 敲低后两种细胞系中有 96 个基因的表达发生了超过 2 倍的变化。10 个上调的共同基因(LPXN、DDR2、COL6A1、IL6、IL8、FYN、PTP4A3、PAPPA、ETV5 和 CYGB)和一个下调的共同基因(CLCA2)被认为增强了肿瘤细胞的侵袭活性。BisoGenet 网络分析表明,NDRG1 以间接方式调节这些侵袭效应基因/蛋白。此外,NDRG1 敲低还降低了 MMP7、TMPRSS4 和 CTSK 等促侵袭基因的表达。这些结果表明,NDRG1 对侵袭和转移的调节是一个高度复杂的过程。