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miR-330-5p suppresses glioblastoma cell proliferation and invasiveness through targeting ITGA5

机译:miR-330-5p通过靶向ITGA5抑制胶质母细胞瘤细胞增殖和侵袭

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摘要

The present study intended to investigate the biological effects of miR-330-5p on glioblastoma (GBM) cell proliferation and invasiveness by targeting integrin α5 (ITGA5). The expressions of miR-330-5p and ITGA5 mRNA in GBM cell lines (U87, U251, and U373) and normal brain glial cell line (HEB) were detected using RT-qPCR. Protein expression of ITGA5 was examined using Western blot. The present study used MTT assay, colony formation assay, Transwell assay, wound healing assay, and flow cytometry analysis in order to determine the biological functions of GBM cells (including cell proliferation, invasion, migration, apoptosis, and cell cycle). The present study applied dual-luciferase reporter gene assay to identify the target relationship between miR-330-5p and ITGA5. miR-330-5p was low-expressed in GBM cell lines while ITGA5 was high-expressed compared with HEB. miR-330-5p could directly target ITGA5 as well as suppress its expression in GBM cells. Up-regulation of miR-330-5p and down-regulation of ITGA5 both have an inhibitory effect on cell proliferation, invasion, and migration. Meanwhile, they could also promote GBM cell apoptosis. miR-330-5p could suppress proliferation and invasion of GBM cells through targeting ITGA5.
机译:本研究旨在通过靶向整联蛋白α5(ITGA5)来研究miR-330-5p对胶质母细胞瘤(GBM)细胞增殖和侵袭性的生物学影响。使用RT-qPCR检测miR-330-5p和ITGA5 mRNA在GBM细胞系(U87,U251和U373)和正常脑胶质细胞系(HEB)中的表达。使用蛋白质印迹检查ITGA5的蛋白质​​表达。为了确定GBM细胞的生物学功能(包括细胞增殖,侵袭,迁移,凋亡和细胞周期),本研究使用MTT分析,集落形成分析,Transwell分析,伤口愈合分析和流式细胞术分析。本研究应用双荧光素酶报告基因测定来确定miR-330-5p与ITGA5之间的靶标关系。与HEB相比,miR-330-5p在GBM细胞系中低表达,而ITGA5在高表达中。 miR-330-5p可以直接靶向ITGA5并抑制其在GBM细胞中的表达。 miR-330-5p的上调和ITGA5的下调均对细胞增殖,侵袭和迁移具有抑制作用。同时,它们还可以促进GBM细胞凋亡。 miR-330-5p可以通过靶向ITGA5抑制GBM细胞的增殖和侵袭。

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