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Magnetofection Based On Superparamagnetic Iron Oxide Nanoparticle-mediated Low LncRNA Hotair Expression Decreases The Proliferation And Invasion Of Glioma Stem Cells

Posted on:2018-06-22Degree:MasterType:Thesis
Country:ChinaCandidate:K FangFull Text:PDF
GTID:2504305897978649Subject:Neurology
Abstract/Summary:PDF Full Text Request
Glioma stem cells(GSCs)are the special subpopulation of glioma cells that are key to the sensitivity of tumors to treatments and to the possibility of tumor recurrence.Identifying new strategies that inhibit the growth of GSCs are therefore important for developing novel therapies for glioblastoma multiform(GBM).In this study,CD133~+human glioma stem cells were isolated and cultured.Magnetic nanoparticles were used to mediate the expression of si RNAs targeting the HOTAIR(si-HOTAIR)sequence in human gliomas.The effect of downregulation of HOTAIR expression on proliferation,invasion and in vivo tumorigenicity of human GSCs and the underlying molecular mechanisms were further evaluated.The results of MTT assay and flow cytometric analysis showed that downregulation of HOTAIR expression inhibited cell proliferation and induced cell cycle arrest.Transwell assays demonstrated that downregulation of HOTAIR expression resulted in a decrease in the invasive capability of GSCs.Moreover,magnetic nanoparticle-mediated low expression of HOTAIR effectively reduced the tumorigenic capacity of glioma stem cells in vivo.In addition,the results of q RT-PCR and western blot analysis demonstrated that downregulation of HOTAIR expression significantly increased the expression of PDCD4 in GSCs,in addition to reducing the expression of CCND1 and CDK4.An in-depth mechanistic analysis showed that downregulation of HOTAIR expression reduced the recruitment of downstream molecules,EZH2 and LSD1,thereby activating the expression of PDCD4 at the transcriptional level.In conclusion,downregulation of HOTAIR expression effectively promoted the expression of PDCD4,thereby inhibiting the proliferation,invasion and in vivo tumorigenicity of human GSCs.
Keywords/Search Tags:Glioma stem cells(GSCs), superparamagnetic iron oxide nanoparticles(SPIONs), HOX transcript antisense RNA(HOTAIR), programed cell death fator4(PDCD4), proliferation, invasion
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