Background: In recent years, the incidence of thyroid cancer (TC), the most common endocrine malignancy, has been increasing. Emerging evidence indicates that the CUT/CUX/CDP family of proteins can play an important role in tumor development and progression by regulating many cancer-related functions. However, the molecular functions of CUX2 in TC remain unknown. Methods: In this study, we used a series of loss-of-function experiments and Western blot analysis to investigate the function of CUX2 in TC and the mechanisms involved. Results: Our data revealed that CUX2 expression levels were upregulated in papillary thyroid cancer (PTC). Functionally, CUX2 silencing significantly inhibited PTC cell line (KTC-1 and BCPAP) proliferation, colony formation, migration, invasion, and apoptosis. Furthermore, CUX2 induced epithelial–mesenchymal transition (EMT) and influenced the phosphorylation of AKT and mTOR in the PI3K–AKT–mTOR pathways. Conclusion: In summary, CUX2 may function as a tumor promoter in TC.
CITATION STYLE
Sun, Y., Ye, D., Li, Y., Chen, E., Hao, R., Cai, Y., … Zhang, X. (2019). Cux2 functions as an oncogene in papillary thyroid cancer. OncoTargets and Therapy, 12, 217–224. https://doi.org/10.2147/OTT.S185710
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