MiR-107 suppresses cell proliferation and tube formation of Ewing sarcoma cells partly by targeting HIF-1β

Hum Cell. 2018 Jan;31(1):42-49. doi: 10.1007/s13577-017-0183-9. Epub 2017 Oct 26.

Abstract

MicroRNAs serve a crucial role in the regulation of malignant biological behavior of Ewing's sarcoma (ES). Abnormal expression of miR-107 has been reported in a cohort of cancers, while its exact function in ES remains unclear. Hence, we explored the expression of miR-107 in ES cells and detected its effects on the malignant phenotype of ES cells. Firstly, we perceived the under-expression of miR-107 in human ES cells contrast with the human mesenchymal stem cells. Over-expression of miR-107 restrained cell proliferation and tube formation, arrested cell cycle progression, and facilitated cell apoptosis in SK-ES-1 and RD-ES cell lines. Furthermore, hypoxia inducible factor-1β (HIF-1β) was assumed as a target gene of miR-107. We confirmed the target role of HIF-1β in ES cells. Finally, restoring the expression of HIF-1β could partly abolish miR-107-mediated tumor suppression in ES cells. In conclusion, our results advised that miR-107 suppressed the malignant biological ability of ES cells through targeting HIF-1β.

Keywords: Ewing’s sarcoma; HIF-1β; MiR-107; Tube formation.

MeSH terms

  • Apoptosis / genetics
  • Aryl Hydrocarbon Receptor Nuclear Translocator / physiology*
  • Cell Cycle Checkpoints / genetics
  • Cell Line, Tumor
  • Cell Proliferation / genetics*
  • Cell Transformation, Neoplastic / genetics*
  • Gene Expression
  • Humans
  • MicroRNAs / physiology*
  • Molecular Targeted Therapy
  • Sarcoma, Ewing / pathology*
  • Sarcoma, Ewing / therapy

Substances

  • ARNT protein, human
  • MIRN107 microRNA, human
  • MicroRNAs
  • Aryl Hydrocarbon Receptor Nuclear Translocator