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李宝林, 邓正华, 常欧, 曾章锐, 刘靳波. miR-494下调Sox9的表达对骨肉瘤细胞MG-63增殖和侵袭的影响[J]. 肿瘤防治研究, 2017, 44(2): 98-102. DOI: 10.3971/j.issn.1000-8578.2017.02.004
引用本文: 李宝林, 邓正华, 常欧, 曾章锐, 刘靳波. miR-494下调Sox9的表达对骨肉瘤细胞MG-63增殖和侵袭的影响[J]. 肿瘤防治研究, 2017, 44(2): 98-102. DOI: 10.3971/j.issn.1000-8578.2017.02.004
LI Baolin, DENG Zhenghua, CHANG Ou, ZENG Zhangrui, LIU Jinbo. miR-494 Inhibits Proliferation and Invasion of Osteosarcoma Cells MG-63 Through Downregulating Sox9 Expression[J]. Cancer Research on Prevention and Treatment, 2017, 44(2): 98-102. DOI: 10.3971/j.issn.1000-8578.2017.02.004
Citation: LI Baolin, DENG Zhenghua, CHANG Ou, ZENG Zhangrui, LIU Jinbo. miR-494 Inhibits Proliferation and Invasion of Osteosarcoma Cells MG-63 Through Downregulating Sox9 Expression[J]. Cancer Research on Prevention and Treatment, 2017, 44(2): 98-102. DOI: 10.3971/j.issn.1000-8578.2017.02.004

miR-494下调Sox9的表达对骨肉瘤细胞MG-63增殖和侵袭的影响

miR-494 Inhibits Proliferation and Invasion of Osteosarcoma Cells MG-63 Through Downregulating Sox9 Expression

  • 摘要:
    目的  探讨miR-494对人骨肉瘤细胞MG-63增殖与侵袭的影响,并验证Sox9是否为miR-494的靶基因。
    方法 过表达miR-494后,利用CCK-8、克隆形成实验检测MG-63细胞的增殖,利用Transwell实验检测细胞的侵袭能力。Western blot与荧光定量PCR检测Sox9蛋白与mRNA水平的表达。
    结果 MG-63细胞转染腺病毒miR-494后,miR-494表达明显升高(t=36.78, P=0.000),Ad-miR-494转染组MG-63细胞增殖(F=1.711, P=0.012)、克隆形成(F=2.742, P=0.019)和侵袭能力(F=1.653, P=0.006)较Ad-GFP组下降。过表达miR-494后,Sox9蛋白(F=5.827, P=0.021)和mRNA表达水平(F=5.827, P=0.021)下降。而Sox9的下调使MG-63细胞增殖(t=27.54, P=0.042)、克隆形成(t=29.64, P= 0.026)和侵袭能力(t=32.48, P=0.016)下降。
    结论 miR-494通过Sox9抑制骨肉瘤细胞MG-63的增殖与侵袭。

     

    Abstract:
    Objective To investigate the impact of miR-494 on the proliferation and invasion of human osteosarcoma cells MG-63 and to confirm whether Sox9 is the target gene of miR-494.
    Methods MG-63 cells were transfected with recombinant adenovirus miR-494(Ad-miR-494), CCK-8 and clone formation experiments were employed to determine the proliferation ability of transfected MG-63 cells. Cells invasion abilities were determined by Transwell assay. Real-time PCR was used to analyze the expression of Sox9 mRNA and protein level to confirmthe adenovirus miR-494 expression in MG-63 cells. The protein expression of Sox9 was analyzed by Western blot.
    Results The expression of miR-494 was increased obviously (t=36.78, P=0.000) in MG-63 cells which were transfected with Ad-miR-494. CCK-8, clone formation and Transwell experiment results revealed that the proliferation (F=1.711, P=0.012), clone formation (F=2.742, P=0.019) and invasion (F=1.653, P=0.006) abilities of MG-63 cells were markedly inhibited by the overexpression of miR-494. In addition, we observed the decreased Sox9 protein (F=5.827, P=0.021) and mRNA expression (F=5.827, P=0.021) in MG-63 cells which were transfected with Ad-miR-494. And the proliferation (t=27.54, P=0.042), lone formation (t=29.64, P=0.026) and invasion (t=32.48, P=0.016) abilities of MG-63 cells were markedly inhibited by the decreases of Sox9 expression.
    Conclusion MG-63 cells proliferation and invasion abilities are suppressed by miR-494, and this process is potentially achieved via suppressing Sox9 expression.

     

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