Alveolar rhabdomyosarcomas in conditional Pax3:Fkhr mice: Cooperativity of Ink4a/ARF and Trp53 loss of function

Charles Keller, Benjamin R. Arenkiel, Cheryl M. Coffin, Nabeel El-Bardeesy, Ronald A. DePinho, Mario R. Capecchi

Research output: Contribution to journalArticlepeer-review

252 Scopus citations


Alveolar rhabdomyosarcoma is an aggressive childhood muscle cancer for which outcomes are poor when the disease is advanced. Although well-developed mouse models exist for embryonal and pleomorphic rhabdomyosarcomas, neither a spontaneous nor a transgenic mouse model of alveolar rhabdomyosarcoma has yet been reported. We report the first mouse model of alveolar rhabdomyosarcoma using a conditional Pax3:Fkhr knock-in allele whose activation in late embryogenesis and postnatally is targeted to terminally differentiating Myf6-expressing skeletal muscle. In these mice, alveolar rhabdomyosarcomas occur but at low frequency, and Fkhr haploinsufficiency does not appear to accelerate tumorigenesis. However, Pax3:Fkhr homozygosity with accompanying Ink4a/ARF or Trp53 pathway disruption, by means of conditional Trp53 or Ink4a/ARF loss of function, substantially increases the frequencies of tumor formation. These results of successful tumor generation postnatally from a target pool of differentiating myofibers are in sharp contrast to the birth defects and lack of tumors for mice with prenatal and postnatal satellite cell triggering of Pax3:Fkhr. Furthermore, these murine alveolar rhabdomyosarcomas have an immunohistochemical profile similar to human alveolar rhabdomyosarcoma, suggesting that this conditional mouse model will be relevant to study of the disease and will be useful for preclinical therapeutic testing.

Original languageEnglish (US)
Pages (from-to)2614-2626
Number of pages13
JournalGenes and Development
Issue number21
StatePublished - Nov 1 2004
Externally publishedYes


  • Alveolar rhabdomyosarcoma
  • Chromosome translocation
  • Fkhr
  • FoxO1A
  • Pax3
  • Pax3:Fkhr
  • Satellite cell

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology


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