MiR-218通过抑制SFMBT1和DCUNIDI的表达影响宫颈癌细胞的侵袭和转移。

Huan Li, Xuzhuo An, Qiaoshan Fu
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引用次数: 2

摘要

宫颈癌是全球第二大常见妇科肿瘤,一直是女性杀手。有研究表明,miR-218可通过sfmbt1和DCUNIDI两个靶基因抑制宫颈癌细胞的侵袭和迁移。在此基础上,本文提出miR-218通过抑制靶基因SFMBT1和DCUNIDI的表达影响宫颈癌细胞的侵袭和迁移的研究。本文采用对照实验进行研究。在荧光实验中,我们证实SFMBT1和DCUNIDI确实是miR-218的下游靶基因。之后,我们通过特异性小干扰RNA和过表达质粒下调或上调SFMBT1和DCUNIDI在宫颈癌细胞中的表达,进行细胞迁移和细胞侵袭实验。细胞侵袭实验结果显示,miR-218组细胞侵袭能力平均值分别为286和218,SFMBT1- sirna1组细胞侵袭能力平均值为264,DCUNIDI-siRNA1组细胞侵袭能力平均值为179,SFMBT1- sirna 2组细胞侵袭能力平均值为245,DCUNIDI-siRNA2组细胞侵袭能力平均值为196,SFMBT1 + miR-218组细胞侵袭能力平均值为401。DCUNIDI + miR-218的平均细胞侵袭性为672。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MiR-218 Affects the Invasion and Metastasis of Cervical Cancer Cells by Inhibiting the Expression of SFMBT1 and DCUNIDI.

As the second most common gynecological tumor in the world, cervical cancer has always been a female killer.Some studies have shown that miR-218 can inhibit the invasion and migration of cervical cancer cells through two target genes, SFMBT1and DCUNIDI. On this basis, this paper presents the study that miR-218 affects the invasion and migration of cervical cancer cells by inhibiting the expression of target genes, SFMBT1 and DCUNIDI. In this paper, we used the control experiment to study. In the fluorescence experiment, we confirmed that SFMBT1 and DCUNIDI are indeed the downstream target genes of miR-218. After that, we down-regulated or up-regulated the expression of SFMBT1 and DCUNIDI in cervical cancer cells through specific small interfering RNA and over-expression plasmids, so we carried out cell migration and cell invasion experiments. The results of the cell invasion experiment showed that the average value of cell invasion ability of the miR-218 group was 286 and 218, that of SFMBT1-siRNA1 was 264, that of DCUNIDI-siRNA1 was 179, that of SFMBT1-siRNA 2 was 245, that of DCUNIDI-siRNA2 was 196, and that of SFMBT1 + miR-218 was 401.The average cell invasiveness of DCUNIDI + miR-218 was 672.

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