Hsa_circ_0008225 inhibits tumorigenesis of glioma via sponging miR-890 and promoting ZMYND11 expression

J Pharmacol Sci. 2020 Jun;143(2):74-82. doi: 10.1016/j.jphs.2020.02.008. Epub 2020 Feb 29.

Abstract

Background: Circular RNAs (circRNAs) play an important role in the tumorigenesis of glioma. Our study indicated that low hsa_circ_0008225 expression was associated with poor overall survival in patients with glioma. However, the relevant mechanism of hsa_circ_0008225 in glioma tumorigenesis remains unclear.

Methods: Two datasets (GSE86202 and GSE92322) were downloaded from the Gene Expression Omnibus (GEO) database. The differentially expressed circRNAs (DEcircRNAs) between glioma tissues and matched normal tissues were screened using R language.

Results: A total of 79 overlapping DEcircRNAs were identified by comparison of glioma and matched normal tissues. In addition, low hsa_circ_0008225 expression was associated with poor overall survival in patients with glioma. Overexpression of hsa_circ_0008225 markedly inhibited the proliferation, migration and invasion of SHG44 cells via inducing apoptosis. Mechanically, overexpression of hsa_circ_0008225 increased the expression of miR-890 targeted gene ZMYND11 via acting as a competitive 'sponge' of miR-890.

Conclusion: Our results suggested that hsa_circ_0008225 functions as a tumor inhibitor in glioma by sponging miR-890 and then promoting the function of ZMYND11. Therefore, hsa_circ_0008225 could be a potential prognostic biomarker for the treatment of glioma.

Keywords: Glioma; Tumorigenesis; ZMYND11; hsa_circ_0008225; microRNA-890.

MeSH terms

  • Apoptosis / genetics
  • Carcinogenesis / genetics*
  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism*
  • Cell Movement / genetics
  • Cell Transformation, Neoplastic / genetics*
  • Co-Repressor Proteins / genetics*
  • Co-Repressor Proteins / metabolism*
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism*
  • Gene Expression
  • Glioma / genetics*
  • Glioma / mortality
  • Glioma / pathology*
  • Humans
  • MicroRNAs*
  • Neoplasm Invasiveness / genetics
  • RNA, Circular / genetics
  • RNA, Circular / physiology*
  • Survival Rate
  • Tumor Cells, Cultured

Substances

  • Cell Cycle Proteins
  • Co-Repressor Proteins
  • DNA-Binding Proteins
  • MIRN890 microRNA, human
  • MicroRNAs
  • RNA, Circular
  • ZMYND11 protein, human