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Updated: Aug 8, 2025

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
TREM2 as a Prognostic Biomarker for Osteosarcoma Microenvironment Remodeling
Zhi-Long Shen1, Zhao-Yu Chen1, Yong Ji2
1Department of Orthopedic Oncology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai 200003, China.
Triggering receptor expressed on myeloid cells-2 (TREM2) is a potential biomarker for osteosarcoma (OS) prognosis. High TREM2 expression correlates with better survival and altered immune cell infiltration within the tumor microenvironment (TME).
Area of Science:
- Oncology
- Immunology
- Bioinformatics
Background:
- The tumor microenvironment (TME) significantly influences osteosarcoma (OS) progression.
- Mechanisms governing immune and stromal components within the OS TME are not fully understood.
Purpose of the Study:
- To identify prognostic biomarkers in osteosarcoma by analyzing transcriptome and clinical data.
- To investigate the role of identified biomarkers in the immune landscape of the OS TME.
Main Methods:
- Utilized transcriptome data from the TARGET database and clinical information for OS patients.
- Employed CIBERSORT and ESTIMATE for immune and stromal cell proportion analysis.
- Applied Protein-Protein Interaction (PPI) networks and Cox regression to identify differentially expressed genes (DEGs) and prognostic biomarkers.
Main Results:
- Triggering receptor expressed on myeloid cells-2 (TREM2) was identified as a significant prognostic biomarker for OS.
- TREM2 expression positively correlated with patient survival time and enrichment of immune function-related genes.
- TREM2 expression showed distinct associations with various tumor-infiltrating immune cells (TICs), including T cells and macrophages.
Conclusions:
- TREM2 plays a crucial role in the immune-related events within the osteosarcoma TME.
- TREM2 may serve as a valuable indicator for TME remodeling and predicting clinical outcomes in OS patients.
- TREM2 presents a potential target for novel immunotherapy strategies in osteosarcoma.
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