MT4-MMP promotes invadopodia formation and cell motility in FaDu head and neck cancer cells

Biochem Biophys Res Commun. 2020 Feb 19;522(4):1009-1014. doi: 10.1016/j.bbrc.2019.12.009. Epub 2019 Dec 5.

Abstract

Hypoxia-inducible factor-1α (HIF-1α) induces cancer metastasis. We previously demonstrated that HIF-1α-induced membrane-type 4 matrix metalloproteinase (MT4-MMP) is involved in hypoxia-mediated metastasis in head and neck squamous cell carcinoma (HNSCC). However, the functions and detailed mechanisms of MT4-MMP in cancer metastasis are not well understood. In this study, we investigated whether MT4-MMP regulates invadopodia formation or individual cell movement-both critical to cancer migration and invasion-in three-dimensional (3D) environments. By expressing MT4-MMP in the HNSCC cell line FaDu, we demonstrated that MT4-MMP increases invadopodia formation and gelatin degradation. Furthermore, the amoeboid-like cell movement on collagen gel was increased by MT4-MMP expression in FaDu cells. Mechanistically, MT4-MMP may induce invadopodia formation by binding with Tks5 and PDGFRα to result in Src activation and promote amoeboid-like movement by stimulating the small GTPases Rho and Cdc42. Altogether, our data indicate that MT4-MMP induces two crucial mechanisms of cancer dissemination, invadopodia formation and amoeboid movement, and elucidate the prometastatic role of MT4-MMP in hypoxia-mediated cancer metastasis.

Keywords: Amoeboid movement; Cell motility; FaDu; HNSCC; Invadopodia; MT4-MMP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism
  • Cardiac Myosins / metabolism
  • Cell Line, Tumor
  • Cell Movement*
  • Gelatin / metabolism
  • HEK293 Cells
  • Head and Neck Neoplasms / enzymology*
  • Head and Neck Neoplasms / pathology*
  • Humans
  • Matrix Metalloproteinases, Membrane-Associated / metabolism*
  • Myosin Light Chains / metabolism
  • Neoplasm Invasiveness
  • Phosphorylation
  • Phosphotyrosine / metabolism
  • Podosomes / pathology*
  • Protein Binding
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism
  • Signal Transduction
  • cdc42 GTP-Binding Protein / metabolism
  • rho GTP-Binding Proteins / metabolism
  • src-Family Kinases / metabolism

Substances

  • Adaptor Proteins, Vesicular Transport
  • Myosin Light Chains
  • SH3PXD2A protein, human
  • myosin light chain 2
  • Phosphotyrosine
  • Gelatin
  • Receptor, Platelet-Derived Growth Factor alpha
  • src-Family Kinases
  • MMP17 protein, human
  • Matrix Metalloproteinases, Membrane-Associated
  • Cardiac Myosins
  • cdc42 GTP-Binding Protein
  • rho GTP-Binding Proteins