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Raf kinase inhibitor protein (RKIP) inhibits the cell migration and invasion in human glioma cell lines in vitro

机译:Raf激酶抑制剂蛋白(RKIP)在体外抑制人胶质瘤细胞系中的细胞迁移和侵袭

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Objective: To investigate the effects and the potential mechanisms of RKIP on cell migration, invasion and proliferation in human glioma cell lines in vitro. Methods: The RKIP over-expressing and RKIP knockdown human U87 glioma cells were used to reveal the effects of RKIP on human glioma cells migration, invasion and proliferation. After the recombinant plasmid pcDNA3.0-RKIP or RKIP-shRNA was transfected into the cell lines U87 by the means of liposome assay, the cells migration, invasion and proliferation were detected by wound healing, Transwell and MTT assay. Then, the levels of RKIP, MMP-3, MMP-9 and HMGA2 mRNA transcription were measured by means of RT-qPCR and levels of proteins expressions were determined using Western blot. Results: The results of MTT assay suggested that the PKIP have little inhibitive effects on glioma cells proliferation (P>0.05). The present paper showed that the migration distances in the group of RKIP-shRNA were markedly increased compared to the pcDNA3.0-RKIP and control. Similarly, the results showed that the numbers of invasion cells in RKIP-shRNA were remarkably increased than the pcDNA3.0-RKIP group and control group. Western blot and RT-qPCR suggested that over-expressions of RKIP lessened the MMP-2, MMP-9 and HMGA2 expression, however, turning down the RKIP expression showed the inverse effects. Conclusion: RKIP inhibits the cells migrations and invasions. Meanwhile, RKIP might inhibit the glioma cells through inhibiting MMPs and HMAG2 expression. Therefore, we demonstrated that RKIP is an underlying target for the treatment of glioma.
机译:目的:探讨RKIP对人胶质瘤细胞体外迁移,侵袭和增殖的影响及其潜在机制。方法:使用RKIP过表达和敲低RKIP的人U87神经胶质瘤细胞来揭示RKIP对人胶质瘤细胞迁移,侵袭和增殖的影响。用脂质体法将重组质粒pcDNA3.0-RKIP或RKIP-shRNA转染到U87细胞株后,通过伤口愈合,Transwell和MTT法检测细胞的迁移,侵袭和增殖。然后,通过RT-qPCR测定RKIP,MMP-3,MMP-9和HMGA2 mRNA的转录水平,并用蛋白质印迹法测定蛋白质表达水平。结果:MTT法检测结果表明PKIP对神经胶质瘤细胞增殖的抑制作用很小(P> 0.05)。结果表明,与pcDNA3.0-RKIP和对照相比,RKIP-shRNA组的迁移距离明显增加。相似地,结果显示,RKIP-shRNA中的侵袭细胞数目比pcDNA3.0-RKIP组和对照组显着增加。 Western印迹和RT-qPCR表明RKIP的过表达降低了MMP-2,MMP-9和HMGA2的表达,但是,降低RKIP的表达则显示出相反的作用。结论:RKIP抑制细胞迁移和侵袭。同时,RKIP可能通过抑制MMPs和HMAG2表达来抑制神经胶质瘤细胞。因此,我们证明了RKIP是治疗神经胶质瘤的潜在靶标。

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