Abstract
Pituitary tumor-transforming gene 1 (PTTG1) has been identified as an oncogene and is overexpressed in many tumor types. However, the role of PTTG1 in glioblastoma (GBM) has not been well characterized, especially in relation to angiogenesis, migration, and invasion. In the present study, our results showed that the expression of PTTG1 was significantly higher in patients with GBM. Bioinformatic analysis showed that angiogenesis and the cell migration-related process were increased in patients with high PTTG1 expression levels; meanwhile, PTTG1 was positively correlated with marker genes of angiogenesis, migration and the evasion of apoptosis. In vitro assays showed that PTTG1 knockdown dramatically suppressed angiogenesis, migration and invasion, and increased the apoptosis of GBM cells. Moreover, our results also showed that silencing PTTG1 suppressed the activity of the TGF-β/PI3K-AKT-mTOR pathway, which induced tumor deterioration in multiple organs. Overall, our findings indicate that PTTG1 is a glioma malignant factor that promotes angiogenesis, migration, invasion, and the evasion of apoptosis, and these roles may be related to the TGF-β/PI3K-AKT-mTOR pathway. Thus, the targeted inhibition of PTTG1 might be a novel therapeutic strategy and a potential diagnostic biomarker for GBM-targeted therapies.
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All data used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Funding
This study was supported by Grants from the Fundamental Research Funds for the Central Universities (No. 20720180042), the Health Science Research Personnel Training Program of Fujian Province (2016-CXB-12), the Natural Science Foundation of Fujian, China (No. 2016D019).
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YLC and JX designed the experiments and drafted the manuscript. CLS, RT, SZH, GXM and FDR performed the study, and ZHT, CSD, ZMS performed the statistical analysis. ZRG revised the manuscript. All authors have read and approved the final manuscript.
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Cui, L., Ren, T., Zhao, H. et al. Suppression of PTTG1 inhibits cell angiogenesis, migration and invasion in glioma cells. Med Oncol 37, 73 (2020). https://doi.org/10.1007/s12032-020-01398-2
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DOI: https://doi.org/10.1007/s12032-020-01398-2