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A novel transformation suppressor, Pdcd4, inhibits AP-1 transactivation but not NF-kappaB or ODC transactivation
- Source :
- Oncogene. 20(6)
- Publication Year :
- 2000
-
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, we 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 was inhibited by 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.
- Subjects :
- Transcriptional Activation
Cancer Research
Tumor suppressor gene
Biology
Ornithine Decarboxylase
Transactivation
chemistry.chemical_compound
Mice
Genetics
Animals
Neoplastic transformation
Genes, Tumor Suppressor
Molecular Biology
NF-kappa B
Proteins
RNA-Binding Proteins
NF-κB
Transfection
Cell biology
Transcription Factor AP-1
Transformation (genetics)
Cell Transformation, Neoplastic
chemistry
Cell culture
Cancer research
Tetradecanoylphorbol Acetate
Tumor promotion
Apoptosis Regulatory Proteins
Subjects
Details
- ISSN :
- 09509232
- Volume :
- 20
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Oncogene
- Accession number :
- edsair.doi.dedup.....1214a92a11e75a264ff8e80960224238