miR-137 suppresses tumor growth of malignant melanoma by targeting aurora kinase A

Biochem Biophys Res Commun. 2016 Jul 1;475(3):251-6. doi: 10.1016/j.bbrc.2016.05.090. Epub 2016 May 24.

Abstract

As an oncogene, aurora kinase A (AURKA) is overexpressed in various types of human cancers. However, the expression and roles of AURKA in malignant melanoma are largely unknown. In this study, a miR-137-AURKA axis was revealed to regulate melanoma growth. We found a significant increase in levels of AURKA in melanoma. Both genetic knockdown and pharmacologic inhibition of AURKA decreased tumor cell growth in vitro and in vivo. Further found that miR-137 reduced AURKA expression through interaction with its 3' untranslated region (3'UTR) and that miR-137 was negatively correlated with AURKA expression in melanoma specimens. Overexpression of miR-137 decreased cell proliferation and colony formation in vitro. Notably, re-expression of AURKA significantly rescued miR-137-mediated suppression of cell growth and clonality. In summary, these results reveal that miR-137 functions as a tumor suppressor by targeting AURKA, providing new insights into investigation of therapeutic strategies against malignant melanoma.

Keywords: Aurora kinase A; Cell growth; Malignant melanoma; miR-137.

MeSH terms

  • Animals
  • Aurora Kinase A / genetics*
  • Cell Line, Tumor
  • Cell Proliferation
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Melanoma / genetics*
  • Melanoma / pathology
  • Mice, Inbred BALB C
  • MicroRNAs / genetics*
  • Skin / pathology*
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology
  • Up-Regulation

Substances

  • MIRN137 microRNA, human
  • MicroRNAs
  • AURKA protein, human
  • Aurora Kinase A