c-Fos mediates α1, 2-fucosyltransferase 1 and Lewis y expression in response to TGF-β1 in ovarian cancer

FUT1 is a key rate-limiting enzyme in the synthesis of Lewis y, a membrane-associated carbohydrate antigen. The aberrant upregulation of FUT1 and Lewis y antigen is related to proliferation, invasion and prognosis in malignant epithelial tumors. A c-Fos/activator protein-1 (AP-1) binding site was found in the FUT1 promoter. However, the mechanisms of transcriptional regulation of FUT1 remain poorly understood. TGF-beta 1 is positively correlated to Lewis y. In the present study, we investigated the molecular mechanism of FUT1 gene expression in response to TGF-beta 1. We demonstrated that c-Fos was highly expressed in 77.50% of ovarian epithelial carcinoma cases and was significantly correlated with Lewis y. Using luciferase activity and chromatin immunoprecipitation (ChIP) assay, we further revealed that c-Fos interacted with the FUT1 promoter in ovarian cancer cells and transcriptional capacity of the heterodimer formed by c-Fos and c-Jun was stronger than that of the c-Fos or c-Jun homodimers. Then, we demonstrated that TGF-beta 1 induced dose-dependent c-Fos expression, which was involved in TGF-beta 1-induced ovarian cancer cell proliferation. In addition, inhibition of MAPK activation or TGF-beta 1 receptor by pharmacological agents prevented TGF-beta 1-induced c-Fos and Lewis y expression. Silencing of c-Fos prevented TGF-beta 1-induced Lewis y expression. Collectively, the results of these studies demonstrated that TGF-beta(1) regulated FUT1 and Lewis y expression by activating the MAPK/c-Fos pathway.