Exosomal lncRNA PVT1/VEGFA Axis Promotes Colon Cancer Metastasis and Stemness by Downregulation of Tumor Suppressor miR-152-3p

• Published in: Oxidative medicine and cellular longevity Vol. 2021; no. 1; p. 9959807
• Main Authors: Lai, Shiue-Wei, Chen, Ming-Yao, Bamodu, Oluwaseun Adebayo, Hsieh, Ming-Shou, Huang, Ting-Yi, Yeh, Chi-Tai, Lee, Wei-Hwa, Cherng, Yih-Giun
• Format: Journal Article
• Language: English
• Published: United States Hindawi 2021; John Wiley & Sons, Inc
• Subjects: Angiogenesis; Animals; Apoptosis; Binding sites; Cell cycle; Cell growth; Cell Line, Tumor; Colonic Neoplasms - genetics; Colonic Neoplasms - pathology; Colorectal cancer; Cyclin-dependent kinases; Disease Progression; Down-Regulation; Drug development; Drug resistance; Exosomes - metabolism; Female; Gene expression; Genes, Tumor Suppressor - physiology; Humans; Kinases; Male; Medical prognosis; Metastasis; Mice; MicroRNAs; MicroRNAs - metabolism; Middle Aged; Neoplasm Metastasis; Proteins; Signal Transduction; Transfection; Tumors; Vascular endothelial growth factor; Vascular Endothelial Growth Factor A - metabolism; United States > US
• DOI: 10.1155/2021/9959807
• ISSN: 1942-0900; 1942-0994

Background. Treating advanced colon cancer remains challenging in clinical settings because of the development of drug resistance and distant metastasis. Mechanisms underlying the metastasis of colon cancer are complex and unclear. Methods. Computational analysis was performed to determine genes associated with the exosomal long noncoding (lncRNA) plasmacytoma variant translocation 1 (PVT1)/vascular endothelial growth factor A (VEGFA) axis in patients with colon cancer. The biological importance of the exosomal lncRNA PVT1/VEGFA axis was examined in vitro by using HCT116 and LoVo cell lines and in vivo by using a patient-derived xenograft (PDX) mouse model through knockdown (by silencing of PVT1) and overexpression (by adding serum exosomes isolated from patients with distant metastasis (M-exo)). Results. The in silico analysis demonstrated that PVT1 overexpression was associated with poor prognosis and increased expression of metastatic markers such as VEGFA and epidermal growth factor receptor (EGFR). This finding was further validated in a small cohort of patients with colon cancer in whom increased PVT1 expression was correlated with colon cancer incidence, disease recurrence, and distant metastasis. M-exo were enriched with PVT1 and VEGFA, and both migratory and invasive abilities of colon cancer cell lines increased when they were cocultured with M-exo. The metastasis-promoting effect was accompanied by increased expression of Twist1, vimentin, and MMP2. M-exo promoted metastasis in PDX mice. In vitro silencing of PVT1 reduced colon tumorigenic properties including migratory, invasive, colony forming, and tumorsphere generation abilities. Further analysis revealed that PVT1, VEGFA, and EGFR interact with and are regulated by miR-152-3p. Increased miR-152-3p expression reduced tumorigenesis, where increased tumorigenesis was observed when miR-152-3p expression was downregulated. Conclusion. Exosomal PVT1 promotes colon cancer metastasis through its association with EGFR and VEGFA expression. miR-152-3p targets both PVT1 and VEGFA, and this regulatory pathway can be explored for drug development and as a prognostic biomarker.