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[靶向微小RNA介导的体外抑制恶性黑色素瘤细胞中血管内皮生长因子基因表达及增殖]

[Targeting microRNA-mediated suppression of vascular endothelial growth factor gene expression and proliferation in malignant melanoma cells in vitro].

作者信息

Jiang Yuan, Han Yongzhi, Sun Jian

机构信息

Department of Dermatology, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2014 Mar;34(3):358-63.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

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