Density and migration of mast cells in lip squamous cell carcinoma and actinic cheilitis

Histol Histopathol. 2009 Apr;24(4):457-65. doi: 10.14670/HH-24.457.

Abstract

Mast cells (MCs) display a diversity of roles that may contribute to the stromal microenvironment alterations during tumor progression. The aim of this study was to investigate MC populations expressing tryptase and c-kit in lip squamous cell carcinoma (lip SCC) (n=37), actinic cheilitis (AC) (n=15) and normal lip mucosa (control) (n=6), as well as their relationship with microscopic parameters (collagen degeneration, elastin changes, angiogenesis and proliferative index). Tryptase, c-kit, CD31 and Ki-67 expressions were analyzed by means of immunohistochemistry and collagen and elastic fibers were visualized with Picrosirus and Verhoeff's stain, respectively. The numbers of tryptase+ MC were significantly higher in lip SCC when compared with control (P=0.01), while a similar density of these cells was observed in AC and lip SCC (P=0.09). The density of c-kit+ MC was similar in all groups examined (P=0.65). MC migration (c-kit+/Tryptase+ relationship) was 69% in lip SCC, 60% in AC and 100% in control. The number of CD31+ blood vessels was significantly higher in the lip SCC when compared with control and AC (P<0.01). The increase of MCs and angiogenesis in lip SCC may reflect an important modification in the tumor microenvironment during squamous photo-carcinogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • Carcinoma, Squamous Cell / blood supply
  • Carcinoma, Squamous Cell / pathology*
  • Carcinoma, Squamous Cell / physiopathology
  • Cell Movement*
  • Cheilitis / pathology*
  • Cheilitis / physiopathology
  • Collagen / metabolism
  • Elastin / metabolism
  • Extracellular Matrix / metabolism
  • Extracellular Matrix / pathology
  • Female
  • Humans
  • Ki-67 Antigen / metabolism
  • Lip Neoplasms / blood supply
  • Lip Neoplasms / pathology*
  • Lip Neoplasms / physiopathology
  • Male
  • Mast Cells / enzymology*
  • Mast Cells / pathology*
  • Middle Aged
  • Mouth Mucosa / blood supply
  • Mouth Mucosa / pathology
  • Mouth Mucosa / physiopathology
  • Neovascularization, Pathologic
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism
  • Proto-Oncogene Proteins c-kit / metabolism
  • Tryptases / metabolism
  • Ultraviolet Rays

Substances

  • Ki-67 Antigen
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Collagen
  • Elastin
  • Proto-Oncogene Proteins c-kit
  • Tryptases