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[微小RNA-16-5p靶向四跨膜蛋白15基因通过磷脂酰肌醇3-激酶/蛋白激酶B信号通路抑制骨肉瘤细胞的增殖、迁移和侵袭]

[microRNA-16-5p targeted tetraspanin 15 gene to inhibit the proliferation, migration and invasion of osteosarcoma cell through phospoinositide 3-kinase/protein kinase B signaling pathway].

作者信息

Yu J B, Zhang H J, Yan L W, Chang F, Jia Z W, Yang X R

机构信息

Orthopedics Departmentof Shanxi Provincial People's Hospital, Taiyuan 030012, China.

Department of Nursing Surgery of Shanxi Health Vocational College, Taiyuan 030607, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2020 Jun 2;100(21):1668-1675. doi: 10.3760/cma.j.cn112137-20191101-02376.

Abstract

To study the effects of miR-16-5p on proliferation, migration and invasion of osteosarcoma cells and its mechanism. Quantitative polymerase chain reaction (qPCR) and Western blotting were used to detect the mRNA and protein expression of miR-16-5p and TSPAN15 in human normal osteoblasts hFOB 1.19 and osteosarcoma cells MG63, Saos2 and HOS. The miR-16-5p or si-TSPAN15 was transfected into MG63 cells to observe its role in cell proliferation, migration and invasion. Cell proliferation was measured with MTT assay, cell migration and invasion were examined by Transwell, and the protein expression of CyclinD1, matrix metalloproteinase 2 (MMP-2), MMP-9, tetraspanin 15 (TSPAN15), phospha-tidylinositol3-kinase(p-PI3K) and phospha-protein kinase B(p-AKT) were determined by using Western blotting. The starbase website prediction combined with dual luciferase gene reporter assay was performed to analyze the targeting relationship between miR-16-5p and TSPAN15. miR-16-5p and pcDNA-TSPAN1 were co-transfected to assess the effect of high expression of TSPAN15 on overexpression of miR-16-5p-induced proliferation, migration and invasion of MG63 cells. Data comparison between the two groups was performed by using test. Compared with hFOB 1.19 cells (1.00±0.12), the expression of miR-16-5p was significantly decreased in MG63, Saos2 and HOS cells (0.32±0.05, 0.40±0.04, 0.45±0.06, respectively)(156.204, 0.05), and TSPAN15 mRNA and protein levels were greatly increased (71.718, 110.350, both 0.05). Overexpression of miR-16-5p obviously reduced the expression of CyclinD1, MMP-2, MMP-9 protein, cell viability, cell migration and invasion (150.136,117.228, 154.971, 89.479, 98.373, 130.880, all 0.05) in MG63 cells. Knockdown of TSPAN15 greatly reduced CyclinD1, MMP-2, MMP-9 protein levels, cell survival rate, cell migration, and invasion number (93.206, 107.030, 109.326, 115.625, 146.113, 139.300, all 0.05). Overexpression of miR-16-5p markedly decreased the expression of p-PI3K and p-AKT protein in MG63 cells (156.755, 181.419, both 0.05). miR-16-5p targeted to regulate the expression of TSPAN15. High expression of TSPAN15 partially reversed the inhibitory effect of miR-16-5p on TSPAN15, CyclinD1, MMP-2, MMP-9, p-PI3K, p-AKT protein expression, cell viability, cell migration number and invasion number in MG63 cells. miR-16-5p inhibits the proliferation, migration and invasion of osteosarcoma cells by targeting the TSPAN15 gene and regulating the PI3K/AKT signaling pathway.

摘要

研究miR-16-5p对骨肉瘤细胞增殖、迁移和侵袭的影响及其机制。采用定量聚合酶链反应(qPCR)和蛋白质免疫印迹法检测人正常成骨细胞hFOB 1.19及骨肉瘤细胞MG63、Saos2和HOS中miR-16-5p和四跨膜蛋白15(TSPAN15)的mRNA和蛋白表达。将miR-16-5p或si-TSPAN15转染至MG63细胞中,观察其对细胞增殖、迁移和侵袭的作用。采用MTT法检测细胞增殖,Transwell法检测细胞迁移和侵袭,蛋白质免疫印迹法检测细胞周期蛋白D1(CyclinD1)、基质金属蛋白酶2(MMP-2)、MMP-9、四跨膜蛋白15(TSPAN15)、磷酸化磷脂酰肌醇3激酶(p-PI3K)和磷酸化蛋白激酶B(p-AKT)的蛋白表达。结合starbase网站预测及双荧光素酶基因报告基因检测分析miR-16-5p与TSPAN15的靶向关系。共转染miR-16-5p和pcDNA-TSPAN1,评估TSPAN15高表达对miR-16-5p过表达诱导的MG63细胞增殖、迁移和侵袭的影响。两组数据比较采用t检验。与hFOB 1.19细胞(1.00±0.12)相比,MG63、Saos2和HOS细胞中miR-16-5p表达显著降低(分别为0.32±0.05、0.40±0.04、0.45±0.06)(t=156.204,P<0.05),而TSPAN15的mRNA和蛋白水平显著升高(t=71.718、110.350,P均<0.05)。miR-16-5p过表达明显降低MG63细胞中CyclinD1、MMP-2、MMP-9蛋白表达、细胞活力、细胞迁移和侵袭能力(t=150.136、117.228、154.971、89.479、98.373、130.880,P均<0.05)。敲低TSPAN15可显著降低CyclinD1、MMP-2、MMP-9蛋白水平、细胞存活率、细胞迁移及侵袭数量(t=93.206、107.030、109.326、115.625、146.113、139.300,P均<0.05)。miR-16-5p过表达显著降低MG63细胞中p-PI3K和p-AKT蛋白表达(t=156.755、181.419,P均<0.05)。miR-16-5p靶向调控TSPAN15表达。TSPAN15高表达部分逆转了miR-16-5p对MG63细胞中TSPAN15、CyclinD1、MMP-2、MMP-9、p-PI3K、p-AKT蛋白表达、细胞活力、细胞迁移数量及侵袭数量的抑制作用。miR-16-5p通过靶向TSPAN15基因并调控PI3K/AKT信号通路抑制骨肉瘤细胞的增殖、迁移和侵袭。

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