基础医学与临床 ›› 2016, Vol. 36 ›› Issue (9): 1227-1231.

• 研究论文 • 上一篇    下一篇

下调microRNA-210增加放射抗拒鼻咽癌细胞的放射敏感性

黎博一1,赵文思1,张露2,周寒静1,秦思1,殷云飞1,张涛1   

  1. 1. 重庆医科大学第一附属医院
    2. 重庆市渝中区袁家岗友谊路1号
  • 收稿日期:2015-10-26 修回日期:2016-01-03 出版日期:2016-09-05 发布日期:2016-08-30
  • 通讯作者: 张涛 E-mail:tumorzzt@163.com
  • 基金资助:
    肿瘤科国家临床重点专科建设项目;重庆市渝中区科技计划项目

Down-regulation of microRNA-210 enhances radiosensitivity in radiation-resistant nasopharyngeal carcinoma cells

  • Received:2015-10-26 Revised:2016-01-03 Online:2016-09-05 Published:2016-08-30

摘要: 目的 研究下调microRNA-210对鼻咽癌放射抗拒细胞的放射敏感性的影响。方法 用剂量梯度法建立鼻咽癌放射抗拒细胞CNE-2R。用microRNA基因芯片检测CNE-2和CNE-2R细胞的miRNAs,用qPCR验证miR-210的相对表达量。用LV-hsa-miR-210-inhibition慢病毒感染CNE-2R细胞,qPCR检测210-inhibition中miR-210的相对表达量,用FCM测CNE-2R和210-inhibition细胞的凋亡和周期,用克隆形成实验测CNE-2R和210-inhibition的存活分数。结果 诱导成功的CNE-2R与CNE-2细胞比较,有93个表达差异>2倍的miRNAs。下调CNE-2R中的miR-210后,与CNE-2R比较,210-inhibition凋亡比例明显增加(P<0.05),处于G2/M期的比例明显增加(P<0.05),S期的比例明显减少(P<0.05), 210-inhibition细胞较CNE-2R细胞的存活分数降低。结论 下调microRNA-210可增加鼻咽癌放射抗拒细胞的放射敏感性,其可能作为治疗放射抗拒的新靶点。

关键词: 鼻咽癌, microRNA-210, 放射抗拒性

Abstract: Objective To explore the effect of miRNA-210 down-regulation on radiosensitivity of radiation-resistant nasopharyngeal carcinoma cells. Methods The radiation-resistant nasopharyngeal carcinoma cells(CNE-2R) were established by dose gradient method. The miRNA microarray was used for detecting miRNA expression profiles of the CNE-2 cells and CNE-2R cells, and miR-210 was verified by qPCR. After LV-hsa-miR-210-inhibition were infected CNE-2R cells, the miR-210 in 210-inhibition cells were verified by qPCR. Apoptosis and cell cycle of 210-inhibition and CNE-2R cells were detected by flow cytometry, the survival fraction of cells were detected by clone formation assay. Results There were 93 miRNAs expression remarkable changed over>2 fold in CNE-2R cell lines which we established, compared with CNE-2. 210-inhibition, which expressing a low level of miR-210 had a higher apoptosis rate than CNE-2R cells(P<0.05). The proportion of 210-inhibition cells in the G2/M phase were more than in the CNE-2R cells(P<0.05), and the S phase of they were less than in the CNE-2R cells(P<0.05). The survival fractions of 210-inhibition cells significantly reduced, compared with CNE-2R cells. Conclusions Down-regulation of microRNA-210 can enhance radiosensitivity in radiation-resistant nasopharyngeal carcinoma cells, which may be used as a new target for the treatment of radiation resistance.

Key words: nasopharyngeal carcinoma, microRNA-210, radiation resistance

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