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MicroRNA-567 inhibits cell proliferation, migration and invasion by targeting FGF5 in osteosarcoma
Daodong Liu1, Chaoju Zhang1, Xiaolin Li2
1Department of Orthopaedics, Jingzhou Hospital of Traditional Chinese Medicine, The Third Clinical College of Yangtze University, Hubei, China.
Abstract:
MicroRNAs (miRNAs) have been widely reported to have important regulatory roles in various human tumors, including osteosarcoma (OS). The aim of this study was to focus on the role of less well-known miRNA-567 (miR-567) in OS. We found the expression of miR-567 was significantly reduced in OS tissues and cell lines (MG-63, U2OS and Saos-2) compared with the adjacent normal tissues and normal osteoblastic cells (hFOB), respectively. Moreover, exogenous miR-567 overexpression inhibited OS cell proliferation, migration and invasion by CCK-8, Transwell assays, respectively. We further explored the mechanism underlying the suppressive effects of miR-567 on OS cells and identified a potential target of miR-567 binds to the 3'UTR of fibroblast growth factor 5 (FGF5) using TargetScan program. Furthermore, enforced expression of miR-567 decreased the expression of FGF5 in both MG-63 and U2OS cells using luciferase reporter assay and Western blotting. We also showed that overexpression of FGF5 could partially antagonize the suppressive effects of miR-567 on OS cell proliferation, migration and invasion. Taken together, our data indicated that miR-567 may function as a tumor suppressor by negatively regulating FGF5 and be potential therapeutic targets for the treatment of OS.
Insights
MicroRNA-567 (miR-567) is reduced in osteosarcoma. Overexpressing miR-567 inhibits tumor growth and invasion by targeting fibroblast growth factor 5 (FGF5), suggesting miR-567 as a potential therapeutic target for osteosarcoma.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) are key regulators in human cancers.
- Osteosarcoma (OS) is a primary bone cancer with significant mortality.
- The specific role of miRNA-567 (miR-567) in OS remains largely unexplored.
Purpose of the Study:
- To investigate the function and mechanism of miR-567 in osteosarcoma.
- To determine the expression levels of miR-567 in OS tissues and cell lines.
- To identify potential targets of miR-567 involved in OS progression.
Main Methods:
- Quantitative real-time PCR to assess miR-567 expression.
- Cell proliferation, migration, and invasion assays (CCK-8, Transwell).
- Bioinformatic analysis (TargetScan), luciferase reporter assays, and Western blotting to validate miR-567 targets.
Main Results:
- miR-567 expression was significantly downregulated in OS tissues and cell lines.
- miR-567 overexpression suppressed OS cell proliferation, migration, and invasion.
- Fibroblast growth factor 5 (FGF5) was identified as a direct target of miR-567, and its expression was negatively regulated by miR-567.
- FGF5 overexpression partially reversed the inhibitory effects of miR-567.
Conclusions:
- miR-567 acts as a tumor suppressor in osteosarcoma.
- The tumor-suppressive role of miR-567 is mediated through the negative regulation of FGF5.
- miR-567 represents a potential therapeutic target for osteosarcoma treatment.
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