Chinese Clinical Oncology

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The effect of microRNA-133b on migration and invasion of glioblastoma

ZHANG Dongzhi, CHANG Liang, SU Jun, WANG Chao, TAN Chunlei, LI Guofu, ZHANG Xuexin.
  

  1. Department of Neurosurgery, the Affiliated Tumor Hospital of Harbin Medical University, Harbin 150081, China
  • Received:2016-11-11 Revised:2017-02-08 Online:2017-05-31 Published:2017-05-31
  • Contact: ZHANG Xuexin

Abstract: Objective To investigate the effect of microRNA-133b (miR-133b) on glioblastoma (GBM) cell and to analyze its possible molecular mechanism. Methods Reverse transcription-polymerase chain reaction(RT-PCR) was used to detect the expression of miR-133b in 20 human GBM samples and normal human glial cells HBE. Transwell migration and invasion assays were used to evaluate the effects of miR-133b on cell migration and invasion. Western blotting and a luciferase reporter assay were used to identify the target genes of miR-133b. Results Compared with the HBE, miR-133b was significantly increased in GBM tissues (1.0±0.17 vs. 2.42±0.69, P<0.05); In Transwell invasion and migration experiments, compared to group transfected with NC, the cells transfected with miR-133b mimic could inhibit the migration and invasion (P<0.05); In Western blotting, compared to cells that transfected with NC, the cells transfected with miR-133b mimic had a lower expression of MMP-14 protein (P<0.05). Furthermore, MMP-14 was identified as a direct target gene of the miR-133b by luciferase reporter gene analysis. Conclusion miR-133b can inhibit the migration and invasion of GBM by direct targeting MMP-14, and it can be used as a candidate target for diagnosis and treatment of GBM.

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