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CD147对LNCaP-AI细胞生长影响

Impact of CD147 on growth of prostate cancer LNCaP-AI cell line

  • 摘要: 目的 观察RNA干扰白细胞分化抗原147(CD147)基因对雄激素非依赖性前列腺癌LNCaP-AI细胞增殖、细胞周期和凋亡影响。方法 脂质体2000转染靶向CD147基因的shRNA质粒到LNCaP-AI细胞中,通过G418筛选获得稳定低表达CD147细胞株。利用溴化四氮唑蓝法和流式细胞术检测CD147基因沉默后对细胞增殖、细胞周期和凋亡的影响。结果 与对照组比较,沉默CD147表达后明显抑制LNCaP-AI细胞增殖(P<0.05);细胞周期出现在G0/G1期细胞百分率从(69.76±3.83)%增加到(79.40±4.02)%,差异有统计学意义(P<0.05);S期和G2/M期细胞百分率分别从(23.51±2.58)%、(6.73±0.70)%减少到(17.03±2.02)%和(3.57±0.21)%,差异有统计学意义(P<0.05),呈现G0/G1期细胞阻滞;但不引起细胞凋亡。结论 RNA干扰CD147基因能够抑制LNCaP-AI细胞增殖,诱导细胞周期异常。

     

    Abstract: Objective To study the effects of targeting cluster of differentiation 147(CD147)RNA interference(RNAi)on cell proliferation,cell cycle and apoptosis of androgen-independent prostate cancer LNCaP-AI cell line.Methods The shRNA vector targeting CD147 gene was transfected into LNCaP-AI cells by Lipofectamine 2000.The stable cell line with down-regulated CD147 was obtained after G418 screening.The cell proliferation,cell cycle and apoptosis were detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and flow cytometry,respectively.Results Compared with the control group,silencing expression of CD147 in LNCaP-AI cell significantly inhibited cell proliferation(P<0.05).The percent of G0/G1 phase cells increased from 69.76±3.83%to 79.40±4.02%(P<0.05),S and G2/M phases cells decreased from 23.51±2.58%to 17.03±2.02%and from 6.73±0.70%to 3.57±0.21%,respectively(P<0.05),which showed that G0/G1 phase of experiment cells were arrested.There was no obvious difference in the RNAi transfected cells in apoptosis.Conclusion Downregulation of CD147 via RNAi technology could decrease the cell proliferation and induce aberrant cell cycle.

     

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