Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Feb 25.
doi: 10.1007/s12306-025-00891-z. Online ahead of print.

Identification of potential genes associated with metastasis in osteosarcoma: an integrated bioinformatics analysis

Affiliations
Review

Identification of potential genes associated with metastasis in osteosarcoma: an integrated bioinformatics analysis

I G E Wiratnaya et al. Musculoskelet Surg. .

Abstract

This study aims to identify the potential genes, pathways, and tumor immune microenvironment that might be involved in the metastasis process of osteosarcoma (OS). The GEO2R tool was deployed to screen two datasets obtained from the Gene Expression Omnibus (GEO) database (GSE87624 and GSE85537). Integrated bioinformatic analyses were then performed to investigate Gene Ontology, potential pathways, protein-protein network interaction, core hub genes, genetic alterations, and immune cell infiltration. The hub gene expression levels were validated utilizing another dataset (GSE14329) and patient prognosis was validated using the GDC-TARGET OS dataset. Our analysis identified 263 differentially expressed genes (DEGs), predominantly associated with the PI3K-AKT signaling pathway. Analysis using Cytoscape based on DEGs revealed five validated core hub genes including COL6A1, MMP2, POSTN, TAGLN, and THY1. Additionally, TAGLN and THY1 have a significant association (P = 0.008) (P = 0.03) with unfavorable outcomes in osteosarcoma patients. This study unveiled that TAGLN and THY1 were associated with metastasis and poor prognosis in OS.

Keywords: Bioinformatics; Differentially expressed genes; Metastasis; Osteosarcoma.

PubMed Disclaimer

Conflict of interest statement

Declarations. Conflict of interest: The authors declare that they have no conflict of interest.

References

    1. Cui J, Dean D, Hornicek FJ et al (2020) The role of extracelluar matrix in osteosarcoma progression and metastasis. J Exp Clin Cancer Res 39:178. https://doi.org/10.1186/s13046-020-01685-w - DOI - PubMed - PMC
    1. Huang X, Zhao J, Bai J et al (2019) Risk and clinicopathological features of osteosarcoma metastasis to the lung: a population-based study. J Bone Oncol 16:100230. https://doi.org/10.1016/j.jbo.2019.100230 - DOI - PubMed - PMC
    1. Marko TA, Diessner BJ, Spector LG (2016) Prevalence of metastasis at diagnosis of osteosarcoma: an international comparison: prevalence of metastatic osteosarcoma at diagnosis. Pediatr Blood Cancer 63:1006–1011. https://doi.org/10.1002/pbc.25963 - DOI - PubMed - PMC
    1. Yang C, Tian Y, Zhao F et al (2020) Bone microenvironment and osteosarcoma metastasis. Int J Mol Sci 21:6985. https://doi.org/10.3390/ijms21196985 - DOI - PubMed - PMC
    1. Lee C-W, Chiang Y-C, Yu P-A et al (2021) A role of CXCL1 drives osteosarcoma lung metastasis via VCAM-1 production. Front Oncol 11:735277. https://doi.org/10.3389/fonc.2021.735277 - DOI - PubMed - PMC

LinkOut - more resources