Invadopodia proteins, cortactin, N-WASP and WIP differentially promote local invasiveness in ameloblastoma

J Oral Pathol Med. 2016 Sep;45(8):591-8. doi: 10.1111/jop.12417. Epub 2016 Jan 11.

Abstract

Background: Cell migration and invasion through interstitial tissues are dependent upon several specialized characteristics of the migratory cell notably generation of proteolytic membranous protrusions or invadopodia. Ameloblastoma is a benign odontogenic epithelial neoplasm with a locally infiltrative behaviour. Cortactin and MMT1-MMP are two invadopodia proteins implicated in its local invasiveness. Other invadopodia regulators, namely N-WASP, WIP and Src kinase remain unclarified. This study addresses their roles in ameloblastoma.

Materials and method: Eighty-seven paraffin-embedded ameloblastoma cases (20 unicystic, 47 solid/multicystic, 3 desmoplastic and 17 recurrent) were subjected to immunohistochemistry for expression of cortactin, N-WASP, WIP, Src kinase and F-actin, and findings correlated with clinicopathological parameters.

Results: Invadopodia proteins (except Src kinase) and F-actin were widely detected in ameloblastoma (cortactin: n = 73/87, 83.9%; N-WASP: n = 59/87; 67.8%; WIP: n = 77/87; 88.5%; and F-actin: n = 87/87, 100%). Protein localization was mainly cytoplasmic and/or membranous, and occasionally nuclear for F-actin. Cortactin, which functions as an actin-scaffolding protein, demonstrated significantly higher expression levels within ameloblastoma tumoral epithelium than in stroma (P < 0.05). N-WASP, which coordinates actin polymerization and invadopodia-mediated extracellular matrix degradation, was overexpressed in the solid/multicystic subtype (P < 0.05). WIP, an upstream regulator of N-WASP, and F-actin were significantly upregulated along the tumour invasive front compared to tumour centres (P < 0.05). Except for males with cortactin overexpression, other clinical parameters (age, ethnicity and anatomical site) showed no significant correlations.

Conclusions: Present results suggest that local invasiveness of ameloblastoma is dependent upon the migratory potential of its tumour cells as defined by their distribution of cortactin, N-WASP and WIP in correlation with F-actin cytoskeletal dynamics.

Keywords: N-WASP; WIP; ameloblastoma; cortactin.

MeSH terms

  • Actins / analysis
  • Actins / biosynthesis
  • Actins / physiology
  • Adolescent
  • Adult
  • Aged
  • Ameloblastoma / metabolism*
  • Ameloblastoma / pathology
  • Cell Movement / physiology
  • Child
  • Cortactin / biosynthesis
  • Cortactin / physiology*
  • Cytoskeletal Proteins / biosynthesis
  • Cytoskeletal Proteins / physiology*
  • Female
  • Humans
  • Immunohistochemistry
  • Intracellular Signaling Peptides and Proteins / biosynthesis
  • Intracellular Signaling Peptides and Proteins / physiology*
  • Jaw Neoplasms / metabolism*
  • Jaw Neoplasms / pathology
  • Male
  • Middle Aged
  • Neoplasm Invasiveness
  • Neoplasms, Glandular and Epithelial / metabolism
  • Podosomes / physiology*
  • Stromal Cells / metabolism
  • Stromal Cells / pathology
  • Wiskott-Aldrich Syndrome Protein, Neuronal / biosynthesis
  • Wiskott-Aldrich Syndrome Protein, Neuronal / physiology*
  • Young Adult
  • src-Family Kinases / analysis
  • src-Family Kinases / physiology

Substances

  • Actins
  • Cortactin
  • Cytoskeletal Proteins
  • Intracellular Signaling Peptides and Proteins
  • WASL protein, human
  • WIPF1 protein, human
  • Wiskott-Aldrich Syndrome Protein, Neuronal
  • src-Family Kinases