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  • Original Paper
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Tumor promoter-induced ornithine decarboxylase gene expression occurs independently of AP-1 activation

Abstract

Activator protein 1 (AP-1) transactivation and ornithine decarboxylase (ODC) activity have been established as essential downstream effectors of mouse skin tumor promotion by 12-O-tetradecanoylphorbol-13-acetate (TPA). Previous studies have shown that inhibition of either AP-1 transactivation or ODC activity suppressed tumor promoter-induced transformation. By utilizing the JB6 mouse epidermal cell system, the present study determined whether TPA-induced ODC gene expression and activity is independent of AP-1 transactivation. In three independent JB6 (P+) clones, stably expressing dominant negative c-jun, TPA-induced ODC gene expression and activity were similar compared to JB6 P+ cells expressing vector-control alone, while AP-1-dependent transcription was inhibited. Transformation-insensitive JB6 (P) cells, which lack TPA-inducible c-jun expression, also exhibited similar induction of ODC activity by TPA. α-Difluoromethylornithine, an irreversible inhibitor of ODC, attenuated, at an equivalent IC50, both TPA-induced ODC activity and anchorage-independent growth of JB6 P+ cells, despite no inhibition of AP-1 transactivation. Taken together, the results presented indicate that TPA-induced ODC gene expression and activity are independent of AP-1 transactivation. Because inhibition of either AP-1 or ODC precludes TPA-induced transformation, and because ODC is independent of AP-1, we propose that there are at least two pathways to transformation. Each pathway is required but not sufficient for transformation.

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Abbreviations

TPA:

12-O-tetradecanoylphorbol-13-acetate

DFMO:

α-difluoromethylornithine

ODC:

ornithine decarboxylase

PKC:

protein kinase C

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Acknowledgements

This work was supported by the National Institutes of Health Grant, R01 CA42585.

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Jansen, A., Colburn, N. & Verma, A. Tumor promoter-induced ornithine decarboxylase gene expression occurs independently of AP-1 activation. Oncogene 18, 5806–5813 (1999). https://doi.org/10.1038/sj.onc.1202965

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