基础医学与临床 ›› 2015, Vol. 35 ›› Issue (4): 458-462.

• 研究论文 • 上一篇    下一篇

宫颈癌组织miRNA-574-5p的表达及其下调后对宫颈癌SiHa细胞的影响

任菲,陈军莹,杜萍,丁楠,赵珊,姚德生   

  1. 广西医科大学附属肿瘤医院
  • 收稿日期:2014-09-19 修回日期:2014-12-28 出版日期:2015-04-05 发布日期:2015-04-08
  • 通讯作者: 姚德生 E-mail:yaodeson@163.com
  • 基金资助:
    衰老调控因子SIRT6与NF-κB对话在人参皂苷Rg1延缓造血干/祖细胞衰老中的作用

Expression of miR-574-5p in tissue with cervical cancer and effects of down-regulation of miR-574-5p on SiHa cell

  • Received:2014-09-19 Revised:2014-12-28 Online:2015-04-05 Published:2015-04-08

摘要: 目的 探讨宫颈癌患者组织中microRNA-574-5p(miR-574-5p)的表达及其下调时对宫颈癌SiHa细胞增殖、凋亡和迁移的影响。 方法 用实时荧光定量PCR测定80例宫颈癌组织中miR-574-5p水平。将miR-574-5p inhibitor转染宫颈癌SiHa细胞,四甲基偶氮唑盐比色法(MTT法)检测细胞增殖能力,流式细胞仪检测细胞凋亡率,tanswell迁移实验检测细胞侵袭能力。 结果 宫颈癌组织中miR-574-5p相对表达水平高于正常宫颈组织(P<0.05);高表达的miR-574-5p与肿块大小、临床分期、病理分级和淋巴结转移有关(P<0.05);转染miR-574-5p inhibitor组与空白组及阴性对照组相比,SiHa细胞增殖能力下降( P<0. 05);细胞凋亡率明显增加( P<0. 05);转染后细胞穿膜能力明显减弱( P<0. 05)。 结论 miR-574-5p的高表达与宫颈癌的进展有关,下调miR-574-5p的表达抑制了宫颈癌SiHa细胞的增殖和迁移,促进其凋亡,有望成为宫颈癌基因治疗的靶点。

关键词: microRNA-574-5p, 宫颈癌, 增殖, 凋亡, 迁移

Abstract: Objective Investigate the expression level of tissue microRNA-574-5p (miR-574-5p) and the effects of down-regulation of miR-574-5p on SiHa cell; Methods The level of tissue miR-574-5p in 80 samples cervical cancer and 60 normal samples as controls were detected by real-time RT-PCR. Transfected the miR-574-5p inhibitor into SiHa cell, and detected the proliferation, the apoptotic rate and the migration of SiHa cell through MTT, the flow cytometer and transwell experiment respectively. Results Expression levels of tissue miR-574-5p was significantly higher in cervical cancer than that in normal controls(P<0.001); Up-regulation expression of miR-574-5p had a significantly positive correlation with the International Federation of Gynecology and Obstetrics (FIGO) stage and pathological grade and lymph node metastasis (P<0.05 ), while it had no clear-cut correlations with the age of patients and menopausal status. After transfected the miR-574-5p inhibitor into SiHa cell, the proliferation and the migration were decline(P<0.05), and the apoptotic rate was addition(P<0.05). Conclusion The high expression of miR-574-5p in the tissue of cervical cancer may be related to the progress in the malignant cervical cancer, which expected to be a potential targeting therapy of cervical cancer through the effects of transfecting miR-574-5p inhibitor on SiHa cell.

Key words: MicroRNA-574-5p, Cervical cancer, proliferation, apoptotic, migration

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