Loss of transcription factor IRF-1 affects tumor susceptibility in mice carrying the Ha-ras transgene or nullizygosity for p53.

نویسندگان

  • H Nozawa
  • E Oda
  • K Nakao
  • M Ishihara
  • S Ueda
  • T Yokochi
  • K Ogasawara
  • Y Nakatsuru
  • S Shimizu
  • Y Ohira
  • K Hioki
  • S Aizawa
  • T Ishikawa
  • M Katsuki
  • T Muto
  • T Taniguchi
  • N Tanaka
چکیده

The transcription factor IRF-1 has been implicated in tumor suppression: IRF-1 suppresses cell transformation and mediates apoptosis in vitro. Here we show that the loss of IRF-1 alleles per se has no effect on spontaneous tumor development in the mouse but dramatically exacerbates previous tumor predispositions caused by the c-Ha-ras transgene or by nullizygosity for p53. Grossly altered tumor spectrum, as compared to p53-null mice, was also observed in mice lacking both IRF-1 and p53, and cells from these mice show significantly higher mutation rate. Our results suggest that IRF-1 is a new member of the tumor susceptibility genes.

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عنوان ژورنال:
  • Genes & development

دوره 13 10  شماره 

صفحات  -

تاریخ انتشار 1999