Knockdown of circular RNA VANGL1 inhibits TGF-β-induced epithelial-mesenchymal transition in melanoma cells by sponging miR-150-5p

J Cell Mol Med. 2021 Dec;25(23):10837-10845. doi: 10.1111/jcmm.16887. Epub 2021 Nov 9.

Abstract

Melanoma is one of the most aggressive and life-threatening skin cancers, and in this research, we aimed to explore the functional role of circular RNA VANGL1 (circVANGL1) in melanoma progression. The expression levels of circVANGL1 were observed to be significantly increased in clinical melanoma tissues and cell lines. Moreover, circVANGL1 knockdown suppressed, while circVANGL1 overexpression promoted the proliferation, migration and invasion abilities of melanoma cells. Further investigations confirmed the direct binding relation between circVANGL1 and miR-150-5p in melanoma, and restoration of miR-150-5p blocked the effects of circVANGL1 overexpression in melanoma cells. We further found that circVANGL1 was up-regulated by TGF-β treatment, and the enhanced EMT of TGF-β-treated melanoma cells was blocked by circVANGL1 knockdown. In conclusion, these results indicated that circVANGL1 might serve as a promising therapeutic target for melanoma.

Keywords: EMT; TGF-β; circular RNA VANGL1; melanoma; miR-150-5p.

MeSH terms

  • Apoptosis / genetics
  • Carrier Proteins / genetics*
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Epithelial-Mesenchymal Transition / genetics*
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Melanoma / genetics*
  • Membrane Proteins / genetics*
  • MicroRNAs / genetics*
  • RNA, Circular / genetics*
  • RNA, Long Noncoding / genetics
  • Skin Neoplasms / genetics
  • Transforming Growth Factor beta / genetics*
  • Up-Regulation / genetics

Substances

  • Carrier Proteins
  • MIRN150 microRNA, human
  • Membrane Proteins
  • MicroRNAs
  • RNA, Circular
  • RNA, Long Noncoding
  • Transforming Growth Factor beta
  • VANGL1 protein, human