The TTYH3/MK5 Positive Feedback Loop regulates Tumor Progression via GSK3-?/? -catenin signaling in HCC

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related death worldwide, and identification of novel targets is necessary for its diagnosis and treatment. This study aimed to investigate the biological function and clinical significance of tweety homolog 3 (TTYH3) in HCC. TTYH3 overexpression promoted cell proliferation, migration, and invasion and inhibited HCCM3 and Hep3B cell apoptosis. TTYH3 promoted tumor formation and metastasis in vivo. TTYH3 upregulated calcium influx and intracellular chloride concentration, thereby promoting cellular migration and regulating epithelial-mesenchymal transition-related protein expression. The interaction between TTYH3 and MK5 was identified through co-immunoprecipitation assays and protein docking. TTYH3 promoted the expression of MK5, which then activated the GSK33/3-catenin signaling pathway. MK5 knockdown attenuated the activation of GSK33/3-catenin signaling by TTYH3. TTYH3 expression was regulated in a positive feedback manner. In clinical HCC samples, TTYH3 was upregulated in the HCC tissues compared to nontumor tissues. Furthermore, high TTYH3 expression was significantly correlated with poor patient survival. The CpG islands were hypomethylated in the promoter region of TTYH3 in HCC tissues. In conclusion, we identified TTYH3 regulates tumor development and progression via MK5/GSK3-3/3-catenin signaling in HCC and promotes itself expression in a positive feedback loop.

Automated summary

This study investigated the biological function and clinical significance of tweety homolog 3 (TTYH3) in hepatocellular carcinoma (HCC). It was found that TTYH3 overexpression promoted cell proliferation, migration, and invasion, inhibited cell apoptosis, and enhanced tumor formation and metastasis in vivo. TTYH3 regulated the MK5/GSK3-β-Catenin signaling pathway and promoted its own expression through a positive feedback loop in HCC.