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pmid:39712483
Exploring the impact of deubiquitination on melanoma prognosis through single-cell RNA sequencing.
Su Peng · Jiaheng Xie · Xiaohu He
Frontiers in genetics · 2024 doi:10.3389/fgene.2024.1509049
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Experiment
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Complete file
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Thus, identifying novel prognostic biomarkers and therapeutic targets is essential.\nMethods: We utilized single-cell RNA sequencing data (GSE215120) from the Gene Expression Omnibus (GEO) database, preprocessing it with the Seurat package. Dimensionality reduction and clustering were executed through Principal Component Analysis (PCA) and Uniform Manifold Approximation and Projection (UMAP). Cell types were annotated based on known marker genes, and the AUCell algorithm assessed the enrichment of deubiquitination-related genes. Cells were categorized into DUB_high and DUB_low groups based on AUCell scores, followed by differential expression analysis. Importantly, we constructed a robust prognostic model utilizing various genes, which was evaluated in the TCGA cohort and an external validation cohort.\nResults: Our prognostic model, developed using Random Survival Forest (RSF) and Ridge Regression methods, demonstrated excellent predictive performance, evidenced by high C-index and AUC values across multiple cohorts. Furthermore, analyses of immune cell infiltration and tumor microenvironment scores revealed significant differences in immune cell distribution and microenvironment characteristics between high-risk and low-risk groups. Functional experiments indicated that TBC1D16 significantly impacts the migration and proliferation of melanoma cells.\nConclusion: This study highlights the critical role of deubiquitination in melanoma and presents a novel prognostic model that effectively stratifies patient risk. The model's strong predictive ability enhances clinical decision-making and provides a framework for future studies on the therapeutic potential of deubiquitination mechanisms in melanoma progression. 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Methods: We utilized single-cell RNA sequencing data (GSE215120) from the Gene Expression Om", "rformed using GraphPad Prism and R software. Single-cell RNA sequencing analysis of cutaneous melanoma microenvironm", "lysis of cutaneous melanoma microenvironment Single-cell RNA sequencing analysis was performed on cutaneous melanoma"], "order_basis": "paper_text_order:26", "id": "assay:1"}, {"role": "data_generation", "definition_id": "rna_seq", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["on on melanoma prognosis through single-cell RNA sequencing.", "essential. Methods: We utilized single-cell RNA sequencing data (GSE215120) from the Gene Expression Om", "g GraphPad Prism and R software. Single-cell RNA sequencing analysis of cutaneous melanoma microenvironm", "aneous melanoma microenvironment Single-cell RNA sequencing analysis was performed on cutaneous melanoma"], "order_basis": "paper_text_order:38", "id": "assay:2"}, {"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["survival_km"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 0.8, "evidence": ["Kaplan-Meier"], "order_basis": "consumes_earlier_output", "id": "assay:3"}]}