Activating GNAS and KRAS mutations in gastric foveolar metaplasia, gastric heterotopia, and adenocarcinoma of the duodenum

A. Matsubara, R. Ogawa, H. Suzuki, I. Oda, H. Taniguchi, Y. Kanai, R. Kushima, S. Sekine

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Background:Heterotopic gastric-type epithelium, including gastric foveolar metaplasia (GFM) and gastric heterotopia (GH), is a common finding in duodenal biopsy specimens; however, there is still controversy regarding their histogenetic backgrounds.Methods:We analysed a total of 177 duodenal lesions, including 66 GFM lesions, 81 GH lesions, and 30 adenocarcinomas, for the presence of GNAS, KRAS, and BRAF mutations.Results:Activating GNAS mutations were identified in 27 GFM lesions (41%) and 23 GH lesions (28%). The KRAS mutations were found in 17 GFM lesions (26%) and 2 GH lesions (2%). A BRAF mutation was found in only one GFM lesion (2%). These mutations were absent in all 32 normal duodenal mucosa specimens that were examined, suggesting a somatic nature. Among the GFM lesions, GNAS mutations were more common in lesions without active inflammation. Analyses of adenocarcinomas identified GNAS and KRAS mutations in 5 (17%) and 11 lesions (37%), respectively. Immunohistochemically, all the GNAS-mutated adenocarcinomas diffusely expressed MUC5AC, indicating gastric epithelial differentiation.Conclusions:A significant proportion of GFM and GH harbours GNAS and/or KRAS mutations. The common presence of these mutations in duodenal adenoma and adenocarcinoma with a gastric epithelial phenotype implies that GFM and GH might be precursors of these tumours.

Original languageEnglish
Pages (from-to)1398-1404
Number of pages7
JournalBritish Journal of Cancer
Volume112
Issue number8
DOIs
Publication statusPublished - 2015 Apr 14
Externally publishedYes

Keywords

  • GNAS
  • Gastric foveolar metaplasia
  • KRAS
  • duodenum
  • gastric heterotopias

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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