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LncRNA SNHG3 Promotes Gastric Cancer Cells Proliferation, Migration, and Invasion by Targeting miR-326

机译:LNCRNA SNHG3通过针对miR-326促进胃癌细胞的增殖,迁移和入侵

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The function and possible mechanism of lncRNA Small Nucleolar RNA Host Gene 3 (SNHG3) in GC have not been fully studied. The aim of our study was to investigate the role of SNHG3 in the proliferation, migration, and invasion of GC cell lines. The expressions of SNHG3, miR-326, and TWIST in GC9811-P GC cell lines were detected by RT-qPCR. Western blotting was performed to detect the protein levels of TWIST and EMT-related genes. Luciferase reporter gene analysis and RNA immunoprecipitation (RIP) analysis confirmed the interaction between lncRNA SNHG3, miR-326, and TWIST. CCK-8 and Transwell assays were performed to detect cell proliferation, invasion, and migration abilities. The results showed that lncRNA SNHG3 and TWIST were highly expressed in GC cell lines, while miR-326 was expressed to a low degree. Moreover, lncRNA SNHG3 knockdown or miR-326 overexpression significantly inhibited cell proliferation, migration, and invasion of GC cell lines. In addition, TWIST overexpression can reverse the inhibition of lncRNA SNHG3 knockdown or miR-326 overexpression on cell proliferation, migration, and invasion. In conclusion, lncRNA SNHG3 may promote GC progression through the miR-326/TWIST axis, which may provide a new diagnostic and prognostic biomarker for GC.
机译:GC中LNCRNA小核仁RNA宿主基因3(SNHG3)的功能和可能机制尚未得到全面研究。我们的研究目的是探讨SNHG3在GC细胞系的增殖,迁移和侵袭中的作用。通过RT-QPCR检测SNHG3,MIR-326和GC9811-P-P GC细胞系中的捻度的表达。进行蛋白质印迹以检测扭曲和EMT相关基因的蛋白质水平。荧光素酶报告基因分析和RNA免疫沉淀(RIP)分析证实了LNCRNA SnHG3,miR-326和扭曲之间的相互作用。 CCK-8和Transwell测定进行检测细胞增殖,侵袭和迁移能力。结果表明,LNCRNA SNHG3和捻度在GC细胞系中高度表达,而MIR-326表示为低程度。此外,LNCRNA SNHG3敲低或miR-326过表达显着抑制了GC细胞系的细胞增殖,迁移和侵袭。此外,扭转过表达可以逆转LNCRNA SNHG3敲低或miR-326过表达对细胞增殖,迁移和侵袭的抑制。总之,LNCRNA SnHG3可以通过MiR-326 /扭转轴促进GC进展,这可能为GC提供新的诊断和预后生物标志物。

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