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Gastrointestinal stromal tumors in a mouse model by targeted mutation of the Kit receptor tyrosine kinase.

Oncogenic Kit mutations are found in somatic gastrointestinal (GI) stromal tumors (GISTs) and mastocytosis. A mouse model for the study of constitutive activation of Kit in oncogenesis has been produced by a knock-in strategy introducing a Kit exon 11-activating mutation into the mouse genome based on a mutation found in a case of human familial GIST syndrome. Heterozygous mutant KitV558Delta/+ mice develop symptoms of disease and eventually die from pathology in the GI tract. Patchy hyperplasia of Kit-positive cells is evident within the myenteric plexus of the entire GI tract. Neoplastic lesions indistinguishable from human GISTs were observed in the cecum of the mutant mice with high penetrance. In addition, mast cell numbers in the dorsal skin were increased. Therefore KitV558Delta/+ mice reproduce human familial GISTs, and they may be used as a model for the study of the role and mechanisms of Kit in neoplasia. Importantly, these results demonstrate that constitutive Kit signaling is critical and sufficient for induction of GIST and hyperplasia of interstitial cells of Cajal.

Pubmed ID: 12754375

Authors

  • Sommer G
  • Agosti V
  • Ehlers I
  • Rossi F
  • Corbacioglu S
  • Farkas J
  • Moore M
  • Manova K
  • Antonescu CR
  • Besmer P

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

May 27, 2003

Associated Grants

  • Agency: BHP HRSA HHS, Id: DH38908
  • Agency: NHLBI NIH HHS, Id: HL/DK55748

Mesh Terms

  • Animals
  • Base Sequence
  • DNA Primers
  • Disease Models, Animal
  • Female
  • Gastrointestinal Neoplasms
  • Gene Targeting
  • Heterozygote
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Transgenic
  • Mutagenesis, Site-Directed
  • Point Mutation
  • Proto-Oncogene Proteins c-kit