K-ras mutation targeted to gastric tissue progenitor cells results in chronic inflammation, an altered microenvironment, and progression to intraepithelial neoplasia

Cancer Res. 2010 Nov 1;70(21):8435-45. doi: 10.1158/0008-5472.CAN-10-1506. Epub 2010 Oct 19.

Abstract

Chronic infectious diseases, such as Helicobacter pylori infection, can promote cancer in a large part through induction of chronic inflammation. Oncogenic K-ras mutation in epithelial cells activates inflammatory pathways, which could compensate for a lack of infectious stimulus. Gastric histopathology and putative progenitor markers [doublecortin and calcium/calmodulin-dependent protein kinase-like 1 (Dcamkl1) and keratin 19 (K19)] in K19-K-ras-V12 (K19-kras) transgenic mice were assessed at 3, 6, 12, and 18 months of age, in comparison with Helicobacter felis-infected wild-type littermates. Inflammation was evaluated by reverse transcription-PCR of proinflammatory cytokines, and K19-kras mice were transplanted with green fluorescent protein (GFP)-labeled bone marrow. Both H. felis infection and K-ras mutation induced upregulation of proinflammatory cytokines, expansion of Dcamkl1(+) cells, and progression to oxyntic atrophy, metaplasia, hyperplasia, and high-grade dysplasia. K19-kras transgenic mice uniquely displayed mucous metaplasia as early as 3 months and progressed to high-grade dysplasia and invasive intramucosal carcinoma by 20 months. In bone marrow-transplanted K19-kras mice that progressed to dysplasia, a large proportion of stromal cells were GFP(+) and bone marrow-derived, but only rare GFP(+) epithelial cells were observed. GFP(+) bone marrow-derived cells included leukocytes and CD45(-) stromal cells that expressed vimentin or α smooth muscle actin and were often found surrounding clusters of Dcamkl1(+) cells at the base of gastric glands. In conclusion, the expression of mutant K-ras in K19(+) gastric epithelial cells can induce chronic inflammation and promote the development of dysplasia.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Blotting, Western
  • Bone Marrow Transplantation
  • Carcinoma in Situ / etiology*
  • Carcinoma in Situ / pathology
  • Cell Proliferation
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Gastric Mucosa / metabolism
  • Helicobacter Infections / metabolism
  • Helicobacter Infections / pathology
  • Helicobacter Infections / virology
  • Helicobacter felis
  • Humans
  • Hyperplasia / etiology
  • Hyperplasia / pathology
  • Hyperplasia / virology
  • Immunoenzyme Techniques
  • In Situ Hybridization
  • Inflammation / etiology*
  • Inflammation / pathology
  • Keratin-19 / genetics
  • Mesenchymal Stem Cells / metabolism
  • Mesenchymal Stem Cells / pathology
  • Metaplasia / etiology
  • Metaplasia / pathology
  • Metaplasia / virology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Muscle, Smooth / cytology
  • Muscle, Smooth / metabolism
  • Mutation / genetics*
  • Neoplasm Invasiveness
  • Precancerous Conditions / etiology*
  • Precancerous Conditions / pathology
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins p21(ras)
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cells / metabolism
  • Stem Cells / pathology*
  • Stem Cells / virology
  • Stomach / pathology
  • Stomach / virology
  • Stomach Neoplasms / etiology*
  • Stomach Neoplasms / pathology
  • Stomach Neoplasms / virology
  • Stromal Cells / metabolism
  • Stromal Cells / pathology
  • Stromal Cells / virology
  • ras Proteins / physiology*

Substances

  • Actins
  • Chemokines
  • Cytokines
  • KRAS protein, human
  • Keratin-19
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Proto-Oncogene Proteins p21(ras)
  • ras Proteins