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A novel transformation suppressor, Pdcd4, inhibits AP-1 transactivation but not NF-kappa B or ODC transactivation

  1. Author:
    Yang, H. S.
    Jansen, A. P.
    Nair, R.
    Shibahara, K.
    Verma, A. K.
    Cmarik, J. L.
    Colburn, N. H.
  2. Author Address

    NCI, Basic Res Lab, Gene Regulat Sect, Frederick, MD 21702 USA. NCI, Basic Res Lab, Gene Regulat Sect, Frederick, MD 21702 USA. Univ Wisconsin, Sch Med, Dept Human Oncol, Madison, WI 53792 USA. Kyoto Univ, Sakyo Ku, Kyoto 606, Japan. Yang HS NCI, Basic Res Lab, Gene Regulat Sect, Frederick, MD 21702 USA.
    1. Year: 2001
  1. Journal: Oncogene
    1. 20
    2. 6
    3. Pages: 669-676
  2. Type of Article: Article
  1. Abstract:

    Pdcd4 is a novel transformation suppressor that is highly expressed in promotion-resistant (P-) mouse epidermal JB6 cells but not in susceptible (P+) cells. Overexpression of pdcd4 cDNA in stably transfected P+ cells rendered cells resistant to tumor promoter-induced transformation, indicating that elevated expression of Pdcd4 protein is sufficient to suppress neoplastic transformation. To determine whether Pdcd4 suppresses neoplastic transformation through inhibiting known transformation required events, se examined the possibility that pdcd4 inhibited the activation of AP-1 or NF-kappaB dependent transcription or of ornithine decarboxylase (ODC) activity. Activation of AP-1-dependent transcriptional activity mas inhibited bai pdcd4 expression in a concentration dependent manner. In contrast, Pdcd4 slightly increased NF-kappaB- dependent transcription and did not alter ODC enzymatic activity. Previous studies suggested that activation of AP-1 was required for P+ cell transformation as well as for tumor promotion in vivo. These results indicate that Pdcd4 functions as a transformation suppressor, possibly through inhibiting AP- 1 activation in combination with other factors such as enhancing NF-kappaB activation. Pdcd4 may thus constitute a useful molecular target for cancer prevention.

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