MiR224-3p inhibits hypoxia-induced autophagy by targeting autophagy-related genes in human glioblastoma cells

Oncotarget. 2015 Dec 8;6(39):41620-37. doi: 10.18632/oncotarget.5871.

Abstract

Human glioblastoma multiforme (GBM) is a malignant solid tumor characterized by severe hypoxia. Autophagy plays a protective role in cancer cells under hypoxia. However, the microRNA (miRNA)-related molecular mechanisms underlying hypoxia-reduced autophagy remain poorly understood in GBM. In this study, we performed a miRNA microarray analysis on GBM cells and found that numerous miRNAs were differentially expressed under hypoxic conditions. Further research showed that miR224-3p, one of the significantly down-regulated miRNAs, was involved in regulating hypoxia-induced autophagy in GBM cells. Overexpression of miR224-3p abolished hypoxia-induced autophagy, whereas knocking down endogenous miR224-3p increased autophagic activity under normoxia. In addition, we demonstrated that miR224-3p inhibited autophagy by directly suppressing the expression of two autophagy-related genes (ATGs), ATG5 and FAK family-interacting protein of 200 kDa (FIP200). Furthermore, in vitro, miR224-3p attenuated cell proliferation and promoted hypoxia-induced apoptosis, and in vivo, overexpression of miR224-3p inhibited tumorigenesis of GBM cells. Collectively, our study identified a novel hypoxia-down-regulated miRNA, miR224-3p, as a key modulator of autophagy by inhibiting ATGs in GBM cells.

Keywords: autophagy; autophagy-related genes; glioblastoma; hypoxia; microRNAs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Animals
  • Apoptosis
  • Autophagy / genetics*
  • Autophagy-Related Protein 5
  • Autophagy-Related Proteins
  • Cell Hypoxia
  • Cell Line, Tumor
  • Cell Proliferation
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Neoplastic
  • Glioblastoma / genetics*
  • Glioblastoma / metabolism
  • Glioblastoma / pathology
  • Heterografts
  • Humans
  • Male
  • Mice, Nude
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Protein Binding
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / metabolism
  • RNA Interference
  • Signal Transduction
  • Time Factors
  • Transfection
  • Tumor Burden
  • Tumor Microenvironment*

Substances

  • 3' Untranslated Regions
  • ATG5 protein, human
  • Autophagy-Related Protein 5
  • Autophagy-Related Proteins
  • MIRN224 microRNA, human
  • MicroRNAs
  • Microtubule-Associated Proteins
  • RB1CC1 protein, human
  • Protein-Tyrosine Kinases