Down-regulation of LINC00472 promotes osteosarcoma tumorigenesis by reducing FOXO1 expressions via miR-300

• Published in: Cancer cell international Vol. 20; no. 1; p. 100
• Main Authors: Zhang, Jingwei, Zhang, Jieyuan, Zhang, Dong, Ni, Weifeng, Xiao, Haijun, Zhao, Bizeng
• Format: Journal Article
• Language: English
• Published: England BioMed Central 30.03.2020; BMC
• Subjects: Binding sites; Bioinformatics; Bone cancer; Bone tumors; Breast cancer; Cell adhesion & migration; Cell growth; Cell proliferation; FOXO1; FOXO1 protein; Laboratory animals; LINC00472; Medical prognosis; Medical research; MicroRNAs; miR-300; Osteosarcoma; Ovarian cancer; Plasmids; Primary Research; Proteins; Sarcoma; Statistical analysis; Tumor suppressor genes; Tumorigenesis; Tumors; Xenografts; United Kingdom > UK; United States > US; China; miR-300; LINC00472; Osteosarcoma; FOXO1
• ISSN: 1475-2867; 1475-2867
• DOI: 10.1186/s12935-020-01170-6

Osteosarcoma (OS) is one of the most common types of primary bone tumors which poses negative effects on the bones of both young children and adolescents. LncRNA LINC00472 has been reported to be involved with poor prognostics in breast cancer and ovarian cancer. As a new lncRNA, its role in OS remains to be elusive. Herein, we are focused to explore its regulatory mechanism in the development of OS. qRT-PCR was utilized to examine the expressions of LINC00472 and miR-300 in OS tissues and cell lines. OS cell lines of U2OS and MG63 were used to investigate the biological function of LINC00472. Xenograft tumor model was built in nude mice with MG63 cells. The expressions of LINC00472 were inhibited in OS tissues and cells, and were negatively related to the expressions of miR-300. LINC00472 directly targeted miR-300. FOXO1 was inhibited in OS tissues and its expressions were negatively related to the expressions of miR-300. LINC00472 over-expressions decreased cell proliferation abilities and colony formation abilities. These effects were mediated by miR-300. The silence of LINC00472 and over-expressions of miR-300 suppressed FOXO1 expressions. LINC00472 greatly reduced tumor growth in vivo and this effect was attenuated by miR-300 mimic. From all the experiments and observations, we demonstrated that LINC00472 could be a potential tumor suppressor in OS through interacting with miR-300 and FOXO1.