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Murine bilateral retinoblastoma exhibiting rapid-onset, metastatic progression and N-myc gene amplification.

Human retinoblastoma is a pediatric cancer initiated by RB gene mutations in the developing retina. We have examined the origins and progression of retinoblastoma in mouse models of the disease. Retina-specific inactivation of Rb on a p130-/- genetic background led to bilateral retinoblastoma with rapid kinetics, whereas on a p107-/- background Rb mutation caused predominantly unilateral tumors that arose with delayed kinetics and incomplete penetrance. In both models, retinoblastomas arose from cells at the extreme periphery of the murine retina. Furthermore, late retinoblastomas progressed to invade the brain and metastasized to the cervical lymph nodes. Metastatic tumors lacking Rb and p130 exhibited chromosomal changes revealed by representational oligonucleotide microarray analysis including high-level amplification of the N-myc oncogene. N-myc was found amplified in three of 16 metastatic retinoblastomas lacking Rb and p130 as well as in retinoblastomas lacking Rb and p107. N-myc amplification ranged from 6- to 400-fold and correlated with high N-myc-expression levels. These murine models closely resemble human retinoblastoma in their progression and secondary genetic changes, making them ideal tools for further dissection of steps to tumorigenesis and for testing novel therapies.

Pubmed ID: 17235288


  • MacPherson D
  • Conkrite K
  • Tam M
  • Mukai S
  • Mu D
  • Jacks T


The EMBO journal

Publication Data

February 7, 2007

Associated Grants

  • Agency: NCI NIH HHS, Id: P01-CA42063
  • Agency: NCI NIH HHS, Id: P30-CA14051

Mesh Terms

  • Animals
  • Blotting, Northern
  • Blotting, Southern
  • Disease Models, Animal
  • Disease Progression
  • Immunohistochemistry
  • Mice
  • Mice, Knockout
  • Neoplasm Metastasis
  • Oligonucleotide Array Sequence Analysis
  • Proto-Oncogene Proteins c-myc
  • Retinoblastoma
  • Retinoblastoma Protein
  • Retinoblastoma-Like Protein p130
  • beta-Galactosidase