Identification of novel target proteins in sebaceous gland carcinoma

Head Neck. 2013 May;35(5):642-8. doi: 10.1002/hed.23021. Epub 2012 Jun 19.

Abstract

Background: The aim of this study was to identify new target proteins in sebaceous gland carcinoma.

Methods: A tissue microarray containing 115 core biopsies was constructed and stained for proteins involved in carcinogenesis, angiogenesis, inflammation, and cell-to-cell contact. Two investigators independently determined protein expression of all antibodies.

Results: Vascular endothelial growth factor receptor 2 (VEGFR-2), platelet-derived growth factor receptor alpha and beta (PDGFR-α/-β), epidermal growth factor receptor (EGFR), cyclooxygenase 1 and 2 (Cox-1/-2), myeloid cell leukemia sequence 1 (Mcl-1), matrix metalloproteinase 1 (MMP-1), CD9, Bmi-1, 14-3-3σ, glutathione S-transferase pi (Gstπ), and members of the sonic hedgehog (SHH), AKT, and WNT pathways were significantly overexpressed in sebaceous gland carcinomas.

Conclusions: We have demonstrated for the first time that proteins related to angiogenesis, inflammation, and cell proliferation are overexpressed in sebaceous gland carcinomas. These proteins may hold promise as novel therapeutic targets for the treatment of sebaceous gland carcinoma.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Cell Adhesion Molecules
  • Cyclooxygenase 1 / metabolism
  • Cyclooxygenase 2 / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Head and Neck Neoplasms / metabolism*
  • Hedgehog Proteins / metabolism
  • Humans
  • Immunohistochemistry
  • Male
  • Matrix Metalloproteinase 1 / metabolism
  • Middle Aged
  • Myeloid Cell Leukemia Sequence 1 Protein / metabolism
  • Neoplasm Proteins / metabolism*
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism
  • Receptor, Platelet-Derived Growth Factor beta / metabolism
  • Sebaceous Gland Neoplasms / metabolism*
  • Tissue Array Analysis
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism
  • Wnt Signaling Pathway / physiology

Substances

  • Cell Adhesion Molecules
  • Hedgehog Proteins
  • Myeloid Cell Leukemia Sequence 1 Protein
  • Neoplasm Proteins
  • SHH protein, human
  • cell aggregation factors
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Receptor, Platelet-Derived Growth Factor alpha
  • Receptor, Platelet-Derived Growth Factor beta
  • Vascular Endothelial Growth Factor Receptor-2
  • Matrix Metalloproteinase 1