SMYD4 promotes MYH9 ubiquitination through lysine monomethylation modification to inhibit breast cancer progression.

• Tác giả: Jun-Ming Cao, Zhao-Hui Chen, Bo-Wen Liu, Xiao-Feng Liu, Rui Sun, Xin Wang, Jin-Shuo Yang, Yue Yu, Xue-Jie Zhou
• Ngôn ngữ: eng
• Ký hiệu phân loại: 302.544 Alienation
• Thông tin xuất bản: England : Breast cancer research : BCR , 2025
• Bộ sưu tập: NCBI
• ID: 50516

Tóm tắt

BACKGROUND: Breast cancer is the leading cause of female mortality worldwide. (SET And MYND Domain Containing 4) SMYD4 has been reported to be a tumour suppressor. However, the molecular mechanism of SMYD4 remains unclear. METHODS: The expression level of SMYD4 in breast cancer cells was detected by qRT-PCR and western blot. The effect of SMYD4 was verified in vitro and in vivo. The interaction between SMYD4 and MYH9 was investigated by co‑IP assay. The regulation of SMYD4 on WNT signaling pathway was detected by luciferase reporter assay and ChIP analysis. RESULTS: This study found that SMYD4 downregulation was associated with poor prognosis. SMYD4 was performed as a tumor suppressor both in vitro and in vivo. SMYD4 was found to interact with the downstream protein MYH9 and impede WNT signaling pathway. Further studies revealed that SMYD4 impeded the binding of MYH9 to the CTNNB1 promoter region by promoting lysine monomethylation and ubiquitination degradation of MYH9. CONCLUSIONS: These findings reveal the emerging character of SMYD4 in Wnt/β‑catenin signaling and bring new sights of gene interaction. The discovery of this SMYD4/MYH9/CTNNB1/WNT/β-Catenin signalling pathway axis suggests that SMYD4 is a potential therapeutic target for breast cancer.