| 引用本文： |
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侯冷晨,孔祥杰,李佳,等.miR-548c-5p对乳腺癌细胞MCF-7的影响[J].同济大学学报（医学版）,2013,34(4):20-25. [点击复制]
- HOU Leng-chen,KONG Xiang-jie,LI Jia,et al.Effect of miR-548c-5p on biological behaviors of breast cancer cell line MCF-7[J].Journal of Tongji University(Medical Science),2013,34(4):20-25. [点击复制]
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| 摘要: |
| 目的研究miR-548c-5p转染乳腺癌MCF-7细胞株后对细胞增殖、迁移及凋亡的影响。方法CCK-8试剂盒检测不同浓度的miR-548c-5p（50、75、100、125、150nmol／L）分别在24、48、72h不同时间点对细胞增殖的影响；miR-548c-5p转染MCF-7乳腺癌细胞株后，荧光定量PCR法检测其转染效率；划痕实验检测细胞迁移能力的变化；流式细胞术分析干扰后细胞周期的变化；荧光显微镜观察转染后乳腺癌细胞凋亡的变化。结果使用RNA干扰技术成功地将miRNA转染入乳腺癌细胞株，使得miR-548c-5p的表达升高。转染后48hmiR-548c-5p浓度为125nmol／L时，对乳腺癌细胞的抑制作用最明显。miR-548c-5p表达上调后细胞G0／G1明显增多，而s期明显减少（P〈0．01），能-定程度上抑制细胞的迁移。荧光显微镜观察发现早期凋亡细胞升高。结论miR-548c-5p通过干扰细胞周期，增加G0／G1期的乳腺癌细胞数，进而抑制细胞增殖。抑制乳腺癌细胞株MCF-7的迁移能力并显著促进其凋亡。miR-548c-5p影响乳腺癌细胞的增殖、迁移和凋亡，有望成为乳腺癌诊疗的靶点之一。 |
| 关键词: 乳腺肿瘤 miR-548c-5p 凋亡 增殖 迁移 |
| DOI：10.3969/j. issnl008 -0392.2013.04.005 |
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| 基金项目:国家自然科学基金（61272240） |
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| Effect of miR-548c-5p on biological behaviors of breast cancer cell line MCF-7 |
| HOU Leng-chen,KONG Xiang-jie,LI Jia,ZHANG Jun-feng,LI Xiao-yu,FANG Lin |
| (Dept. of Anesthesiology, Tenth People＇s Hospital, Tongji University, Shanghai 200072, China;Dept. of General Surgery, Tenth People＇s Hospital, Tongji University, Shanghai 200072, China)) |
| Abstract: |
| Objective To investigate the effects of miR-548c-5p on biological behaviors of MCF-7 breast cancer cell line. Methods The growth inhibition rates of human breast cancer MCF-7 cells were determined by CCK-8 kits after treated with different concentrations of miR-548c-5p （50, 75, 100, 125 and 150 nmol/L） at different time points （24, 48 and 72 h）. MCF-7 breast cancer cells were transfected with miR-548c-5p by Lipofectamine 2000 and the transfection efficiency was measured by QRT-PCR method. Cell invasion ability was assessed by scratch assay, cell cycle changes were analyzed by flow cytometry, cell apoptosis was observed by fluorescence microscopy in breast cancer MCF-7 cells after transfection with miR-548c-5p. Results The expression of miR-548c-5p was significantly enhanced after transfection （P 〈 0. 01 ）. MiR-548c-5p significantly inhibited the proliferation of MCF-7 breast tumor cells at 48 h after transfection with the concentration of 125 nmol/L. Compared with controls, cells in G0/G1 phase increased, while cells in S phase decreased（ P 〈 0.01 ）. The invasion ability of MCF-7 cells was suppressed and the early apoptotic cells were increased after transfection. Conclusion MiR-548c-5p can increase G0/G1 phase, inhibit cell proliferation and invasion and induce apoptosis of human breast cancer MCF-7 cells, indicating that miR-548c-5p may be used as a new target for treatment of breast cancer. |
| Key words: breast cancer miR-548c-5p apoptosis proliferation invasion |
