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MicroRNA-145-3p suppresses proliferation and promotes apotosis and autophagy of osteosarcoma cell by targeting HDAC4  期刊论文  

  • 编号:
    a0c13ce0-f73a-4ce2-b555-e0436f42302d
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  • 语种:
    英文
  • 期刊:
    ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY ISSN:2169-1401 2018 年 46 卷 (579 - 586)
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  • 摘要:

    Studies have shown that miR-145-3p functions as a tumor suppressor and is associated with tumor growth and metastasis. This study intends to uncover the mechanism of a tumor suppressor of miR-145-3p. The expressions of miR-194 in osteosarcoma cell lines and tissues were monitored by real-time PCR. The proliferation ability was examined by MTT assay. The apoptosis and autophagy of cells were monitored by flow cytometry and microcopy, respectively. The regulation of miR-145-3p on HDAC4 was determined by luciferase assays and western blot assay. The results showed that miR-145-3p was significantly reduced in the osteosarcoma compared with the normal bone tissue. Overexpression of miR-145-3p significantly attenuated the proliferation and induced the apoptosis and autophagy of osteosarcoma cells. Furthermore, we demonstrated that miR-145-3p has inhibited the malignant behavior of osteosarcoma by down-regulating HDAC4 expression. These findings suggested that miR-145-3p may act as a tumor suppressor in osteosarcoma. MiR-145-3p/HDAC4 may be a novel therapeutic target in treatment of osteosarcoma.

  • 推荐引用方式
    GB/T 7714:
    Wu Guangzhi,Yu Wei,Zhang Minglei, et al. MicroRNA-145-3p suppresses proliferation and promotes apotosis and autophagy of osteosarcoma cell by targeting HDAC4 [J].ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY,2018,46:579-586.
  • APA:
    Wu Guangzhi,Yu Wei,Zhang Minglei,Yin Ruofeng,&Liu Qiang.(2018).MicroRNA-145-3p suppresses proliferation and promotes apotosis and autophagy of osteosarcoma cell by targeting HDAC4 .ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY,46:579-586.
  • MLA:
    Wu Guangzhi, et al. "MicroRNA-145-3p suppresses proliferation and promotes apotosis and autophagy of osteosarcoma cell by targeting HDAC4" .ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY 46(2018):579-586.
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