目的:探讨miR-17-5p抑制物对于骨肉瘤细胞系SOSP_9607细胞增殖和凋亡的影响。方法:四甲基偶氮唑蓝(MTT)法测定细胞增殖,进一步计算抑制率,流式细胞仪测定细胞凋亡。将SOSP_9607细胞分为对照组和实验组,对照组分为阴性对照和正常细胞对照组。实验组采用miR-17-5p抑制物(hsa-miR-17-5pinhibitors)抑制SOSP_9607细胞内miR-17-5p的活性。结果:与对照组相比,实验组显著抑制SOSP_9607细胞的增殖,有明显的剂量依赖性(P〈0.01)。随着浓度从50nmol/L逐渐增加至200nmol/L,抑制率逐渐增高(P〈0.01)。实验组凋亡率(9.6±1.8)%与阴性对照组凋亡率(3.5±0.4)%相比明显增高(P〈0.01)。结论:miR-17-5p抑制物通过抑制SOSP_9607细胞中miR-17-5p的活性对SOSP_9607细胞的增殖和凋亡发挥重要作用。
Objective:To determine the effects of microRNA-17-5p inhibitors on proliferation and apoptosis of human osteosarcoma cell line SOSP-9607.Methods:MTT assay was used to examine the inhibitive percentage of hsa-miR-17-5p inhibitors on the proliferation of SOSP-9607 cells.Cultured SOSP-9607 cells were divided into two groups:control group and experimental group.The control group contained two groups:the negtive control and the normal control.In experimental group,hsa-miR-17-5p inhibitors were used to inhibit the activity of miR-17-5p.It contained three groups with different doses.The apoptosis and the cell cycle were 1measured by flow cytometry.Cultured SOSP-9607 cells were also divided into two groups:control group and experimental group.Results:Hsa-miR-17-5p inhibitors inhibited SOSP-9607 cell proliferation in a dose-dependent manner(P0.01),while the control group had no obvious effects on cell proliferation(P0.05).With the increment of concentration of inhibitors from 50 nmol/L to 200 nmol/L,the inhibition percentage increased significantly (P0.01).The apoptosis ratio of experimental group([9.6±1.8)%] was obviously higher than the apoptosis ratio of control group ([3.5±0.4)%](P0.01).Conclusions:The hsa-miR-17-5p inhibitors plays an important role in cell proliferation and apoptosis in SOSP-9607 cells by down-regulated the miR-17-5p.