FOXP4 promotes laryngeal squamous cell carcinoma progression through directly targeting LEF-1

Forkhead box (FOX) proteins are multifaceted transcription factors that have been shown to be involved in cell cycle progression, proliferation and metastasis. FOXP4, a member of the FOX family, has been implicated in diverse biological processes in tumor initiation and progression. However, the molecular mechanisms of FOXP4 in laryngeal squamous cell carcinoma (LSCC) remain unknown. In the present study, differentially expressed transcripts in transforming growth factor-beta-treated TU177 cells were screened using microarrays and it was found that FOXP4 was significantly upregulated. The high expression of FOXP4 was detected in LSCC tissues and cells, and predicted poor prognosis. The role of FOXP4 in laryngeal cancer cell proliferation, migration and invasion was determined by gain- and loss-of-function assays. Besides, FOXP4 was demonstrated to participate in the epithelial-mesenchymal transition process at the mRNA and protein levels. Mechanically, FOXP4 directly bound to the promoter of lymphoid enhancer-binding factor 1 and activated Wnt signaling pathway, which was confirmed via chromatin immunoprecipitation and luciferase reporter assays. Consequently, these findings provided novel mechanisms of FOXP4 in LSCC progression, which may be considered as potential therapeutic and prognostic targets for LSCC.

Automated summary

FOXP4, a member of the FOX family, is significantly upregulated in LSCC tissues and cells and is associated with poor prognosis. It plays a role in cell proliferation, migration, invasion, and epithelial-mesenchymal transition, by directly binding to the promoter of lymphoid enhancer-binding factor 1 and activating the Wnt signaling pathway. These findings suggest potential therapeutic and prognostic targets for LSCC.