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Oncogenesis of the lens in transgenic mice.

Abstract
Neoplastic tumors of the ocular lens of vertebrates do not naturally occur. Transgenic mice carrying a hybrid gene comprising the murine alpha A-crystallin promoter (-366 to +46) fused to the coding sequence of the SV40 T antigens developed lens tumors, which obliterated the eye cavity and even invaded neighboring tissue, thus establishing that the lens is not refractive to oncogenesis. Large-T antigen was detected early in lens development; it elicited morphological changes and specifically interfered with differentiation of lens fiber cells. Both alpha- and beta-crystallins persisted in many of the lens tumor cells, while gamma-crystallin was selectively reduced. Accessibility, characteristic morphology, and defined protein markers make this transparent epithelial eye tissue a potentially useful system for testing tumorigenicity of oncogenes and for studying malignant transformation from its inception until death of the animal.
AuthorsK A Mahon, A B Chepelinsky, J S Khillan, P A Overbeek, J Piatigorsky, H Westphal
JournalScience (New York, N.Y.) (Science) Vol. 235 Issue 4796 Pg. 1622-8 (Mar 27 1987) ISSN: 0036-8075 [Print] United States
PMID3029873 (Publication Type: Journal Article)
Chemical References
  • Antigens, Polyomavirus Transforming
  • Antigens, Viral, Tumor
  • Crystallins
  • Oncogene Proteins, Viral
Topics
  • Animals
  • Antigens, Polyomavirus Transforming
  • Antigens, Viral, Tumor (analysis)
  • Cell Transformation, Neoplastic
  • Cell Transformation, Viral
  • Chimera
  • Crystallins (analysis)
  • Eye Neoplasms (pathology)
  • Female
  • Lens Diseases (pathology)
  • Lens, Crystalline (growth & development)
  • Mice (genetics)
  • Oncogene Proteins, Viral (analysis)
  • Phenotype
  • Pregnancy
  • Simian virus 40
  • Transcription, Genetic

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