Axl contributes to efficient migration and invasion of melanoma cells

PLoS One. 2023 Mar 29;18(3):e0283749. doi: 10.1371/journal.pone.0283749. eCollection 2023.

Abstract

Axl, a member of the TAM receptor family has been broadly suggested to play a key role in tumor metastasis. However, the function of Axl in the invasion and metastasis of melanoma, the most lethal skin cancer, remains largely unknown. In the present study, we found that melanoma cell lines present variable protein levels of Axl and Tyro3; interestingly, MerTK is not noted at detectable levels in any of tested MGP (metastatic growth phase) cell lines. Treatment with recombinant human Gas6 significantly activates Akt in the Axl-expressing WM852 and IgR3 lines but just slightly in WM1158. IgR3, WM852 and WM1158 demonstrate different autocrine signaling. Knockdown of Axl by siRNA or the treatment with Axl-specific inhibitor R428 dramatically inhibits the migration and invasion of both IgR3 and WM852 in vitro. These findings suggest that Axl enhances the invasion of melanoma cells.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Axl Receptor Tyrosine Kinase* / genetics
  • Cell Line, Tumor
  • Humans
  • Melanoma* / genetics
  • Melanoma* / pathology
  • Neoplasm Invasiveness
  • Phosphorylation
  • Receptor Protein-Tyrosine Kinases
  • Recombinant Proteins
  • Signal Transduction
  • Skin Neoplasms* / genetics
  • Skin Neoplasms* / pathology
  • c-Mer Tyrosine Kinase

Substances

  • AXL protein, human
  • Axl Receptor Tyrosine Kinase
  • growth arrest-specific protein 6
  • Recombinant Proteins
  • TYRO3 protein, human
  • Receptor Protein-Tyrosine Kinases
  • MERTK protein, human
  • c-Mer Tyrosine Kinase