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pmid:38049463
Identification and validation of a T cell marker gene-based signature to predict prognosis and immunotherapy response in gastric cancer.
Jinlin Zhong · Rongling Pan · Miao Gao · Yuqian Mo · Xin Peng · Guoxiao Liang · Zixuan Chen · Jinlin Du · Zhigang Huang
Scientific reports · 2023 doi:10.1038/s41598-023-48930-8
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Experiment
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Analysis
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Execution
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Complete file
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In this work, we analyzed the single-cell RNA sequencing data set in GSE183904 and identified 322 T cell marker genes using the \"FindAllMarkers\" method of the R package \"Seurat\". STAD patients in the TCGA database were divided into high-risk and low-risk categories based on risk scores. The five-gene prediction signature based on T cell marker genes can predict the prognosis of gastric cancer patients with high accuracy. In the training cohort, the areas under the receiver operating characteristic (ROC) curve were 0.667, 0.73, and 0.818 at 1, 3, and 5 years. External validation of the predictive signature was also performed using multiple clinical subgroups and GEO cohorts. To help with practical application, a diagnostic model was created that shows values of 0.732, 0.752, and 0.816 for the relevant areas under the ROC curve at 1, 3, and 5 years. 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"parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 1.0, "band": "verbatim", "quote": "To reduce overfitting and choose the best prognostic genes, we used the LASSO approach with Cox proportional hazards regression."}}, {"id": "method-2", "family": "group_comparison", "specific": "wilcoxon", "label": "Group comparison", "dsl_operations": [], "missing_operations": ["group_comparison_wilcoxon"], "expressible": false, "parameters": {}, "data_shapes": ["two_or_more_groups_continuous"], "evidence": {"score": 0.8, "band": "high", "quote": "Wilcoxon"}}, {"id": "method-3", "family": "principal_component_analysis", "specific": "pca", "label": "Principal component analysis", "dsl_operations": ["pca_fit"], "missing_operations": [], "expressible": true, "parameters": {"n_components": "Top 15 principal components (PCs) from the top 2,00"}, "data_shapes": ["wide_numeric_matrix"], "evidence": {"score": 0.8, "band": "high", "quote": "principal component 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The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE183904", "GSE62254", "GSE84437", "GSE84433"], "resolved_accessions": ["GSE183904", "GSE62254", "GSE84437", "GSE84433"], "statements": ["The entire set of findings presented here is based on information from TCGA, available at https://www.cancer.gov/tcga, and the GEO database, accessible at https://www.ncbi.nlm.nih.gov/geo/, with accession numbers GSE183904, GSE62254, GSE84437, and GSE84433."], "basis": "The paper names GSE183904, GSE62254, GSE84437, GSE84433 in GEO and the accession resolves in the repository. 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In this work, we analyzed the single-cell RNA sequencing data set in GSE183904 and identified 322 T c", "Materials and methods Method Analysis of scRNA-seq data scRNA-seq data was processed using the", "nd methods Method Analysis of scRNA-seq data scRNA-seq data was processed using the R packages “Seu", "e R packages “Seurat” and “SingleR”9,10. The scRNA-seq data quality control method started by exclu"], "order_basis": "paper_text_order:333", "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": 0.93, "evidence": ["d. In this work, we analyzed the single-cell RNA sequencing data set in GSE183904 and identified 322 T c"], "order_basis": "paper_text_order:345", "id": "assay:2"}, {"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["cox_ph"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["To reduce overfitting and choose the best prognostic genes, we used the LASSO approach with Cox proportional hazards regression."], "order_basis": "consumes_earlier_output", "id": "assay:3"}]}