Differential expression of the epithelial mesenchymal transition factors Snail, Slug, Twist, TGF-β, and E-cadherin in ameloblastoma

Med Mol Morphol. 2017 Jun;50(2):68-75. doi: 10.1007/s00795-016-0149-0. Epub 2016 Dec 19.

Abstract

Epithelial mesenchymal transition (EMT), the transition of epithelial cells into motile mesenchymal cells, plays an important role in embryogenesis, cancer invasion, and metastasis. Ameloblastomas are common epithelial odontogenic tumors, occurring exclusively in the mandible with locally invasive growth. Thirty-seven ameloblastoma cases were evaluated for the involvement of EMT by immunohistochemical staining and western blotting using antibodies against Slug, Snail, Twist, TGF-β, and E-cadherin. Double immunostaining was also performed. Slug and TGF-β were expressed in the nuclei of peripheral and stellate reticulum cells of ameloblastoma nests. Twenty cases of Snail, 36 of Slug, 8 of Twist, and 19 of TGF-β showed strong expression in tumor cells in follicular and plexiform patterns. Expression of Slug and TGF-β increased in regions where the expression of E-cadherin was reduced. EMT was found to be associated with the local invasive growth of ameloblastoma. These data suggest that reduced expression of E-cadherin and over-expression of Slug, Snail, and TGF-β induce EMT. Given that ameloblastomas are characterized by local invasiveness, EMT might be related to their development. Thus, strong expression of Slug and TGF-β and reduced expression of E-cadherin might be related to the local invasiveness of ameloblastoma.

Keywords: Ameloblastoma; Double immunostaining; E-cadherin; Epithelial mesenchymal transition (EMT); Immunohistochemistry; Slug; Snail.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Ameloblastoma / genetics*
  • Ameloblastoma / metabolism
  • Ameloblastoma / pathology
  • Antigens, CD
  • Cadherins / genetics*
  • Cadherins / metabolism
  • Child
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Epithelial-Mesenchymal Transition / genetics*
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Immunohistochemistry
  • Male
  • Mandibular Neoplasms / genetics*
  • Mandibular Neoplasms / metabolism
  • Mandibular Neoplasms / pathology
  • Middle Aged
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Snail Family Transcription Factors / genetics*
  • Snail Family Transcription Factors / metabolism
  • Transforming Growth Factor beta1 / genetics*
  • Transforming Growth Factor beta1 / metabolism
  • Twist-Related Protein 1 / genetics
  • Twist-Related Protein 1 / metabolism

Substances

  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • Nuclear Proteins
  • SNAI1 protein, human
  • Snail Family Transcription Factors
  • TGFB1 protein, human
  • TWIST1 protein, human
  • Transforming Growth Factor beta1
  • Twist-Related Protein 1