Jiang Yuan, Han Yongzhi, Sun Jian
Department of Dermatology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China. E-mail:
Nan Fang Yi Ke Da Xue Xue Bao. 2014 Mar;34(3):358-63.
To explore the inhibitory effect of targeting miRNA on the expression of vascular endothelial growth factor (VEGF) and cell proliferation in malignant melanoma (MM) SKmel-28 cells.
Recombination miRNA plasmid vectors targeting VEGF gene were transfected into SKmel-28 cells via Lipofectamine 2000. The integrity of the inserted fragments was detected using colony PCR and sequence analysis. The expression of VEGF mRNA and protein in SKmel-28 cells was detected by RT-PCR and Western blotting, respectively. MTS assay was used to determine the inhibitory effect of a selected targeting miRNA on SKmel-28 cell proliferation, and the apoptosis of SKmel-28 cells was detected using flow cytometry.
Transfection with the targeting miRNAs significantly down-regulated the expressions of VEGF mRNA and protein in SKmel-28 cells (P<0.01), and the miRNA construct X-26-2n-1 showed the highest inhibitory effect. The miRNA X-26-2n-1 significantly suppressed SKmel-28 cell proliferation in a time-dependent manner (P<0.01) and increased the early, late and overall apoptosis rates of the cells (P<0.01).
The targeting miRNA we constructed can effectively suppress the cell proliferation and induce apoptosis of SKmel-28 cells by down-regulating the expressions of VEGF gene.
探讨靶向微小RNA(miRNA)对恶性黑色素瘤(MM)SKmel-28细胞中血管内皮生长因子(VEGF)表达及细胞增殖的抑制作用。
通过脂质体2000将靶向VEGF基因的重组miRNA质粒载体转染至SKmel-28细胞。采用菌落PCR和序列分析检测插入片段的完整性。分别通过逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测SKmel-28细胞中VEGF mRNA和蛋白的表达。采用MTS法测定筛选出的靶向miRNA对SKmel-28细胞增殖的抑制作用,并用流式细胞术检测SKmel-28细胞的凋亡情况。
转染靶向miRNA后,SKmel-28细胞中VEGF mRNA和蛋白的表达显著下调(P<0.01),其中miRNA构建体X-26-2n-1的抑制作用最强。miRNA X-26-2n-1以时间依赖性方式显著抑制SKmel-28细胞增殖(P<0.01),并增加细胞的早期、晚期及总体凋亡率(P<0.01)。
我们构建的靶向miRNA可通过下调VEGF基因的表达有效抑制SKmel-28细胞的增殖并诱导其凋亡。