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pmid:37662777
Prognostic value of GLCE and infiltrating immune cells in Ewing sarcoma.
Jian Wen · Lijun Yi · Lijia Wan · Xieping Dong
Heliyon · 2023 doi:10.1016/j.heliyon.2023.e19357
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Experiment
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Complete file
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Common differentially expressed genes between normal subjects and ES patients in GSE17679, GSE45544, and GSE68776 were identified and screened by multiple algorithms to find hub genes with prognostic value. The prognostic value of 64 infiltrating cells was also explored. A prognostic model was established and then validated with GSE63155 and GSE63156. Finally, functional analysis was performed.\nResults: GLCE and mast cell infiltration were screened as two indicators for a prognostic model. The Kaplan‒Meier analysis showed that patients in the low GLCE expression, mast cell infiltration and risk score groups had poorer outcomes than patients in the high GLCE expression, mast cell infiltration and risk score groups, both in the training and validation sets. Scatter plots and heatmaps also indicated the same results. The concordance indices and calibration analyses indicated a high prediction accuracy of the model in the training and validation sets. The time-dependent receiver operating characteristic analyses suggested high sensitivity and specificity of the model, with area under the curve values between 0.76 and 0.98. The decision curve analyses suggested a significantly higher net benefit by the model than the treat-all and treat-none strategies. Functional analyses suggested that glycosaminoglycan biosynthesis-heparan sulfate/heparin, the cell cycle and microRNAs in cancer were upregulated in ES patients.\nConclusions: GLCE and mast cell infiltration are potential prognostic indicators in ES. GLCE may affect the proliferation, angiogenesis and metastasis of ES by affecting the biosynthesis of heparan sulfate and heparin.", "claims": [{"id": "claim-method", "statement": "DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37662777", "locator": "sections[4] \"Identification of common DEGs and prognostic genes\" paragraph 2", "quote": "DEGs between the normal subjects and ES patients were identified by this package in the GSE17679, GSE68776, and GSE45544 sets (|log2FC| > 1 and adjusted p value < 0.05). Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). Thereafter, least absolute shrinkage and selection operator (LASSO) regression analysis (λ = 1 se) [18,19] and random forest (RF) feature selection [20,21] were used to screen prognostic genes."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available data sets were analyzed in this study. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE17679"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE17679"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37662777", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1016/j.heliyon.2023.e19357", "sha256": "sha256:1c3c4fe1b19d2b94f6cee8e38d0e2434186dda3c36c738860e59b231704f29c8", "bytes": 57377, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1016/j.heliyon.2023.e19357", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC10474439", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE17679", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE17679", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE17679", "version": null, "note": "Publicly available data sets were analyzed in this study. 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Then, common DEGs in the three sets were selected for subsequent screening. Univariate Cox regression analysis with a p value < 0.05 was used to identify genes directly associated with the survival of ES. Kaplan‒Meier analysis was then adopted to screen potential prognostic genes with a p value < 0.05 between the high and low expression groups (stratified by median). 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