PTEN Methylation Dependent Sinonasal Mucosal Melanoma

Cancer Res Treat. 2016 Apr;48(2):853-8. doi: 10.4143/crt.2014.356. Epub 2015 Mar 18.

Abstract

Sinonasal mucosal melanoma (SMM) is an aggressive and rare type of melanoma. Although the classic RAS-RAF-MEK pathway is thought to be the main pathway involved in melanoma pathogenesis, genetic alterations in the phosphatidylinositol 3-kinase-AKT pathway, including PTEN-regulated signaling, are also thought to contribute. So far, data regarding altered PTEN expression and epigenetic mechanism of PTEN silencing in development of SMM is extremely limited. Herein we report on a case of SMM with liver and bone metastases with an epigenetic alteration of PTEN. Results of mutation analysis for BRAF, NRAS, HRAS, KRAS, PIK3CA, c-Kit, and PTEN were negative; however, methylation of PTEN CpG islands was observed. Our case not only supports PTEN as a major tumor suppressor involved in melanoma tumorigenesis, but also a potential epigenetic mechanism of PTEN silencing in development of SMM.

Keywords: Methylation; Phosphatase and tensin homolog; Sinonasal melanoma.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Neoplasms / secondary
  • Carcinogenesis / genetics*
  • CpG Islands / genetics
  • DNA Methylation*
  • DNA Mutational Analysis
  • Epigenesis, Genetic*
  • Female
  • Humans
  • Liver Neoplasms / secondary
  • Melanoma / enzymology
  • Melanoma / genetics*
  • Melanoma / metabolism
  • Melanoma / pathology*
  • Middle Aged
  • Mutation
  • PTEN Phosphohydrolase / genetics*
  • PTEN Phosphohydrolase / metabolism
  • Signal Transduction

Substances

  • PTEN Phosphohydrolase