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作 者:刘胄[1] 吴兴洲[1] 宋锐[1] 宗训付 汝磊 李凯[2] 赵庆华[2]
机构地区:[1]阜阳市肿瘤医院骨一科,安徽236000 [2]上海交通大学附属第一人民医院骨科
出 处:《中华医学杂志》2013年第13期1028-1031,共4页National Medical Journal of China
摘 要:目的观察沉默环氧合酶2(COX-2)基因对人骨肉瘤细胞SaOS2生长及转移的影响。方法利用慢病毒介导的RNA干扰技术沉默人骨肉瘤细胞SaOS2中内源性COX-2基因的表达,应用MTF和迁移实验等分别检测COX-2沉默对SaOS2增殖能力、迁移能力的影响;应用实时聚合酶链反应和免疫印迹检测COX-2、血管内皮生长因子(VEGF)、表皮生长因子(EGF)、成纤维细胞生长因子(bFGF)的mRNA和蛋白表达水平。结果转染LV-COX-2siRNA-1沉默COX-2后,SaOS2细胞生长受到了明显的抑制,直接降低了SaOS2细胞的迁移率;并能显著抑制VEGFA,EGF和bFGF的表达,而VEGFB和VEGFC的含量没有明显变化。结论RNA沉默人骨肉瘤中COX-2的表达能显著抑制SaOS2细胞的生长,降低其转移能力,并能下调VEGF、EGF和bFGF的mRNA和蛋白质的表达水平。Objective To explore the effects of a knockdown of cyclooxygenase 2 upon the growth and migration of SaOS2 cells. Methods We employed lentivirus mediated-RNA interference technology to knockdown the endogenous expression of gene COX-2 in human osteosarcoma cells ( SaOS: ) and analyzed their phenotypical changes. The effects of COX-2 silencing on the proliferation, cell cycle and migration of SaOS2 cells were assessed by thiazoyl blue tetrazolium bromide, flow eytometry and migration assays respectively. COX-2, vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), basic fibroblast growth factor (bFGF) mRNA and protein expression were detected by reverse transcription- polymerase chain reaction (RT-PCR) and Western blot. Results A decreased expression of COX-2 in human osteosarcoma cells significantly inhibited the growth and decreased the migration ability of SaOS2 cells. Furthermore, it also reduced VEGF, EGF and bFGF mRNA and protein expression. Conclusion The COX-2 signaling pathway may provide a novel therapeutic target for the treatment of human osteosareoma.
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