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pmid:38256356

Comprehensive Analysis Reveals Prognostic and Therapeutic Immunity-Related Biomarkers for Pediatric Metastatic Osteosarcoma.

Jin Yuan · Shengji Yu

Medicina (Kaunas, Lithuania) · 2024 doi:10.3390/medicina60010095

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Experiment

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Data

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Comprehensive Analysis Reveals Prognostic and Therapeutic Immunity-Related Biomarkers for Pediatric Metastatic Osteosarcoma.
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10.3390/medicina60010095
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Jin Yuan
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Shengji Yu
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Medicina (Kaunas, Lithuania)
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2024
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Background and Objectives: Osteosarcoma, the most prevalent malignant bone tumor in children and adolescents, presents a complex pathogenesis characterized by various genetic and epigenetic alterations. This study aims to identify key differentially expressed genes (DEGs) in pediatric osteosarcoma, with a focus on those influencing metastasis and patient survival. Materials and Methods: We utilized the GSE33382 dataset from the GEO database for a comprehensive bioinformatic analysis. This included a protein-protein interaction (PPI) network analysis, Cox regression, and Kaplan-Meier survival analysis to identify central DEGs associated with osteosarcoma metastasis and patient survival. Results: Our analysis identified 88 DEGs related to osteosarcoma metastasis. Among them, three survival-related central DEGs-C1QA, CD74, and HLA-DMA-were significantly linked to patient outcomes. Further correlation analysis established a strong relationship between these genes, tumor mutation burden (TMB), immune checkpoint gene expression, and overall survival. Notably, C1QA and CD74 exhibited higher expression in non-metastatic osteosarcoma cases, suggesting a potential role in disease progression. Conclusions: The identified DEGs, particularly C1QA, CD74, and HLA-DMA, may serve as critical biomarkers for pediatric osteosarcoma prognosis and potential targets for immunotherapy. These findings provide a deeper understanding of the molecular landscape of osteosarcoma and open new avenues for therapeutic intervention.
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A Kaplan–Meier (KM) survival analysis with the log-rank test was also used to compare the survival difference between the above two groups. For Kaplan–Meier curves, p-values and hazard ratios (HRs) with 95% confidence intervals were generated by log-rank tests and univariate Cox proportional hazards regression with the R package (survival and survminer).
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A Kaplan–Meier (KM) survival analysis with the log-rank test was also used to compare the survival difference between the above two groups. For Kaplan–Meier curves, p-values and hazard ratios (HRs) with 95% confidence intervals were generated by log-rank tests and univariate Cox proportional hazards regression with the R package (survival and survminer).
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The datasets analyzed for this study are available in publicly accessible repositories. The GSE33382 dataset was obtained from the GEO database. The TARGET-osteosarcoma dataset and GEPIA database were also utilized. These datasets were used under the open access guidelines provided by each database.
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Our analysis identified 88 DEGs related to osteosarcoma metastasis. Among them, three survival-related central DEGs—C1QA, CD74, and HLA-DMA—were significantly linked to patient outcomes.
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This study aims to identify key differentially expressed genes (DEGs) in pediatric osteosarcoma, with a focus on those influencing metastasis and patient survival. Materials and Methods: We utilized the GSE33382 dataset from the GEO database for a comprehensive bioinformatic analysis. This included a protein-protein interaction (PPI) network analysis, Cox regression, and Kaplan-Meier survival analysis to identify central DEGs associated with osteosarcoma metastasis and patient survival. Results: Our analysis identified 88 DEGs related to osteosarcoma metastasis. Among them, three survival-related central DEGs-C1QA, CD74, and HLA-DMA-were significantly linked to patient outcomes. Further correlation analysis established a strong relationship between these genes, tumor mutation burden (TMB), immune checkpoint gene expression, and overall survival. Notably, C1QA and CD74 exhibited higher expression in non-metastatic osteosarcoma cases, suggesting a potential role in disease progression. 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