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miR-3189-3p 模拟物通过靶向 CFL2 增强 S100A4 siRNA 抑制胃癌细胞增殖和迁移的作用。

miR-3189-3p Mimics Enhance the Effects of S100A4 siRNA on the Inhibition of Proliferation and Migration of Gastric Cancer Cells by Targeting CFL2.

机构信息

Department of Medical Genetics, China Medical University, Shenyang 110122, China.

Teaching and Experiment Center, Liaoning University of Traditional Chinese Medicine, Shenyang110847, China.

出版信息

Int J Mol Sci. 2018 Jan 13;19(1):236. doi: 10.3390/ijms19010236.

DOI:10.3390/ijms19010236
PMID:29342841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5796184/
Abstract

is a downstream gene of . miR-3189 is embedded in the intron of -and coexpressed with it. miR-3189-3p functions to inhibit the proliferation and migration of glioblastoma cells. We speculated that might regulate miR-3189-3p to affect its function in gastric cancer cells. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) showed that miR-3189-3p expression was significantly downregulated in MGC803 cells after knockdown. Overexpression of miR-3189-3p significantly inhibited the proliferation and migration of the cells. Moreover, miR-3189-3p mimics enhanced the effects of an siRNA on the inhibition of cell proliferation and migration. Dual luciferase reporter assays, qRT-PCR, and Western blotting verified that is a direct target of miR-3189-3p. mediates the regulation of miR-3189-3p on the proliferation and migration of MGC803 cells. Data mining based on Kaplan-Meier plots showed that high expression is associated with poor overall survival and first progression in gastric cancer. These data suggested that miR-3189-3p mimics enhanced the effects of the siRNA on the inhibition of gastric cancer cell proliferation and migration by targeting . The findings suggested that when targeting to treat gastric cancer, consideration and correction for counteracting factors should obtain a satisfactory effect.

摘要

是下游基因。miR-3189 嵌入 - 的内含子中,并与其共表达。miR-3189-3p 可抑制神经胶质瘤细胞的增殖和迁移。我们推测可能通过调节 miR-3189-3p 来影响其在胃癌细胞中的功能。实时定量逆转录聚合酶链反应 (qRT-PCR) 显示,敲低后 MGC803 细胞中 miR-3189-3p 的表达明显下调。miR-3189-3p 的过表达显著抑制了细胞的增殖和迁移。此外,miR-3189-3p 模拟物增强了 an siRNA 对细胞增殖和迁移抑制的作用。双荧光素酶报告基因检测、qRT-PCR 和 Western blot 验证了是 miR-3189-3p 的直接靶基因。调节 miR-3189-3p 对 MGC803 细胞增殖和迁移的作用。基于 Kaplan-Meier 图的数据挖掘表明,高表达与胃癌患者总生存期和首次进展不良相关。这些数据表明,miR-3189-3p 模拟物通过靶向增强了 an siRNA 对胃癌细胞增殖和迁移的抑制作用。这些发现表明,在针对治疗胃癌时,应考虑和纠正对抗因素,以获得满意的效果。

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