FGFR3 mutations in epidermal nevi and seborrheic keratoses: lessons from urothelium and skin

J Invest Dermatol. 2007 Jul;127(7):1572-3. doi: 10.1038/sj.jid.5700772.

Abstract

Somatic FGFR3 mutations have been reported in various cancers such as urothelial carcinoma. Evidence is growing that these mutations are also involved in the pathogenesis of benign acanthotic skin tumors such as epidermal nevi and seborrheic keratoses. The report by Hernandez et al. strongly supports this concept. However, further studies are required for a better pathogenetic understanding of FGFR3 related tumors in urothelium and skin.

Publication types

  • Comment

MeSH terms

  • DNA, Neoplasm / genetics
  • Germ-Line Mutation / genetics*
  • Humans
  • Keratosis, Seborrheic / genetics*
  • Keratosis, Seborrheic / metabolism
  • Nevus / genetics*
  • Nevus / metabolism
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics*
  • Receptor, Fibroblast Growth Factor, Type 3 / metabolism
  • Skin / metabolism
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / metabolism
  • Urinary Bladder Neoplasms / genetics*
  • Urinary Bladder Neoplasms / metabolism
  • Urothelium / metabolism

Substances

  • DNA, Neoplasm
  • FGFR3 protein, human
  • Receptor, Fibroblast Growth Factor, Type 3