Differentiation-inducing factor-1 suppresses gene expression of cyclin D1 in tumor cells |
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Authors: | Yasmin Tania Takahashi-Yanaga Fumi Mori Jun Miwa Yoshikazu Hirata Masato Watanabe Yutaka Morimoto Sachio Sasaguri Toshiyuki |
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Affiliation: | Department of Clinical Pharmacology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan. |
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Abstract: | To determine the mechanism by which differentiation-inducing factor-1 (DIF-1), a morphogen of Dictyostelium discoideum, inhibits tumor cell proliferation, we examined the effect of DIF-1 on the gene expression of cyclin D1. DIF-1 strongly reduced the expression of cyclin D1 mRNA and correspondingly decreased the amount of beta-catenin in HeLa cells and squamous cell carcinoma cells. DIF-1 activated glycogen synthase kinase-3beta (GSK-3beta) and inhibition of GSK-3beta attenuated the DIF-1-induced beta-catenin degradation, indicating the involvement of GSK-3beta in this effect. Moreover, DIF-1 reduced the activities of T-cell factor (TCF)/lymphoid enhancer factor (LEF) reporter plasmid and a reporter gene driven by the human cyclin D1 promoter. Eliminating the TCF/LEF consensus site from the cyclin D1 promoter diminished the effect of DIF-1. These results suggest that DIF-1 inhibits Wnt/beta-catenin signaling, resulting in the suppression of cyclin D1 promoter activity. |
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Keywords: | Wnt signal GSK-3β β-Catenin TCF/LEF Cyclin D1 Differentiation-inducing factor Gene expression HeLa Squamous cell carcinoma |
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