目的 观察过表达微小RNA124(miR-124)对宫颈癌Siha细胞放射敏感性的影响,并探讨其机制.方法 将宫颈癌Siha细胞分为观察组和对照组,观察组转染miR-124模拟物,对照组不转染.采用实时荧光定量PCR法检测两组细胞miR-124和信号转导和转录激活因子3(STAT3)mRNA表达量.采用克隆形成实验检测两组细胞放射敏感性.采用流式细胞术检测两组细胞周期分布和放射后细胞凋亡率.结果 观察组、对照组D0分别为1.062、1.542 Gy,Dq分别为1.605、1.970 Gy,SF2分别为0.527、0.685.观察组相对于对照组的放射增敏比为1.451.转染后24h观察组、对照组miR-124相对表达量分别为89.3±13.6、1.0±0.1,STAT3 mRNA相对表达量分别为0.3±0.03、1.0±0.1,两组相比,P均<0.05.观察组G 0/G1期细胞比例为82.49%±1.97%、S期细胞比例11.87%±1.38%、G 2/M期细胞比例为5.64%±0.72%;对照组分别为74.58%±1.28%、19.88%±0.26%、5.54%±1.05%.观察组G 0/G1期比例高于对照组组,S期比例低于对照组(P均<0.05),两组G 2/M期细胞比例相比P>0.05.观察组、对照组细胞X线照射后细胞凋亡率分别为45.87%±3.16%、37.27%±0.87%,两组相比,P<0.05.结论 过表达miR-124可能提高宫颈癌Siha细胞的放射敏感性.其机制可能是过表达miR-124会抑制宫颈癌Siha细胞STAT3表达,进而阻滞细胞周期于G0/G1期,促进细胞凋亡,从而提高宫颈癌Siha细胞的放射敏感性.%Objective To observe the effect of microRNA124 (miR-124)overexpression on the radiosensitivity of cervical cancer Siha cells and its mechanism. Methods The cervical cancer Siha cells were divided into the observation group and control group. The miR-124 mimics were transfected into the observation group. The expression levels of miR-124 and signal transducer and activator of transcription 3 (STAT3)in the two groups were detected by real-time fluorescent quantitative PCR. Colony formation assay was used to detect the radiosensitivity of the two groups cells. Clone formation as-say was used to detect the cell radiosensitivity. Flow cytometry was used to detect the cell cycle distritution and apoptosis rate after radiation. Results The observation group and the control group had the D0 parameters of 1. 062 Gy and 1. 542 Gy,the Dq parameters of 1. 605Gy and 1. 970Gy,the SF2 parameters of 0. 527 and 0. 685,respectively. Compared with the control group,the radiation sensitization enhancement ratio (SER)was 1. 451. At 24 h after transfection,the relative expression levels of miR-124 in the observation group and the control group were 89. 3 ± 13. 6 and 1. 0 ± 0. 1,respectively, and the relative expression levels of STAT3 mRNA were 0. 3 ± 0. 03 and 1. 0 ± 0. 1,respectively;significant difference was found between these two groups (all P < 0. 05). In the observation group,the percentage of cells in G 0 / G1 phase was 82. 49% ± 1. 97%,was 11. 87% ± 1. 38% in S phase,and 5. 64% ± 0. 72% in G 2 / M phase;meanwhile,they were 74. 58% ± 1. 28%,19. 88% ± 0. 26%,5. 54% ± 1. 05%,respectively,in the control group. Compared with the control group,the percentage of cells in G 0 / G1 phase was higher,while the percentage of cells in S phase was lower,and signifi-cant difference was found between these two groups (all P < 0. 05). Compared with the control group,the percentage of cells in G2 / M phase was not significantly different (P > 0. 05). The apoptosis rates after X-irradiation were 45. 87% ± 3. 16% in observation group,versus 37. 27% ± 0. 87% in the control group,and significant difference was found between these two groups (P < 0. 05). Conclusions Overexpression of miR-124 may enhance radiosensitivity of cervical cancer Si-ha cells. The mechanism may be that overexpression of miR-124 can inhibit the expression of STAT3 in cervical cancer Siha cells,and then induce the cell cycle arrest in G 0 / G1 phase,promote the apoptosis,and thereby enhance the radiosensitivity of cervical cancer Siha cells.
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