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pmid:35783254

A Novel Extracellular Matrix Gene-Based Prognostic Model to Predict Overall Survive in Patients With Glioblastoma.

Chen Qian · Wu Xiufu · Tang Jianxun · Chen Zihao · Shi Wenjie · Tang Jingfeng · Ulf D Kahlert · Du Renfei

Frontiers in genetics · 2022 doi:10.3389/fgene.2022.851427

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Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35783254
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title
A Novel Extracellular Matrix Gene-Based Prognostic Model to Predict Overall Survive in Patients With Glioblastoma.
doi
10.3389/fgene.2022.851427
pmid
35783254
authors array · 8 items
[0]
Chen Qian
[1]
Wu Xiufu
[2]
Tang Jianxun
[3]
Chen Zihao
[4]
Shi Wenjie
[5]
Tang Jingfeng
[6]
Ulf D Kahlert
[7]
Du Renfei
journal
Frontiers in genetics
year
2022
abstract
Background: Glioblastoma (GBM), one of the most prevalent brain tumor types, is correlated with an extremely poor prognosis. The extracellular matrix (ECM) genes could activate many crucial pathways that facilitate tumor development. This study aims to provide online models to predict GBM survival by ECM genes. Methods: The associations of ECM genes with the prognosis of GBM were analyzed, and the significant prognosis-related genes were used to develop the ECM index in the CGGA dataset. Furthermore, the ECM index was then validated on three datasets, namely, GSE16011, TCGA-GBM, and GSE83300. The prognosis difference, differentially expressed genes, and potential drugs were obtained. Multiple machine learning methods were selected to construct the model to predict the survival status of GBM patients at 6, 12, 18, 24, 30, and 36 months after diagnosis. Results: Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis. GBM patients were divided into high- and low-ECM index groups with significantly different overall survival rates in four datasets. High-ECM index patients exhibited a worse prognosis than low-ECM index patients. Four small molecules (podophyllotoxin, lasalocid, MG-262, and nystatin) that might reduce GBM development were predicted by the Cmap dataset. In the independent dataset (GSE83300), the maximum values of prediction accuracy at 6, 12, 18, 24, 30, and 36 months were 0.878, 0.769, 0.748, 0.720, 0.705, and 0.868, respectively. These machine learning models were provided on a publicly accessible, open-source website (https://ospg.shinyapps.io/OSPG/). Conclusion: In summary, our findings indicated that ECM genes were prognostic indicators for patient survival. This study provided an online server for the prediction of survival curves of GBM patients.
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We used a univariate Cox regression analysis in CGGA, GSE16011, and TCGA-GBM to examine the links between ECM gene (1,936 unique ECM-related genes from 47 ECM gene sets) expression and overall survival (OS).
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sections[4] "Construction and Validation of the ECM Index" paragraph 2
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We used a univariate Cox regression analysis in CGGA, GSE16011, and TCGA-GBM to examine the links between ECM gene (1,936 unique ECM-related genes from 47 ECM gene sets) expression and overall survival (OS).
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.
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Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis.
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Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis.
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Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis.
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title
Intrinsic Gene Expression Profiles of Gliomas are a Better Predictor of Survival than Histology
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We used a univariate Cox regression analysis in CGGA, GSE16011, and TCGA-GBM to examine the links between ECM gene (1,936 unique ECM-related genes from 47 ECM gene sets) expression and overall survival (OS).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35783254", "kind": "science-record", "revision": 4, "content_hash": "sha256:d6342e2d96a9cb3e99385d420f5c657e6c86729d52ad2e5b9f53c8b9f1af02f9", "created_at": "2026-11-01T18:14:48Z", "updated_at": "2026-11-01T22:06:55Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A Novel Extracellular Matrix Gene-Based Prognostic Model to Predict Overall Survive in Patients With Glioblastoma.", "doi": "10.3389/fgene.2022.851427", "pmid": "35783254", "authors": ["Chen Qian", "Wu Xiufu", "Tang Jianxun", "Chen Zihao", "Shi Wenjie", "Tang Jingfeng", "Ulf D Kahlert", "Du Renfei"], "journal": "Frontiers in genetics", "year": 2022, "abstract": "Background: Glioblastoma (GBM), one of the most prevalent brain tumor types, is correlated with an extremely poor prognosis. The extracellular matrix (ECM) genes could activate many crucial pathways that facilitate tumor development. This study aims to provide online models to predict GBM survival by ECM genes. Methods: The associations of ECM genes with the prognosis of GBM were analyzed, and the significant prognosis-related genes were used to develop the ECM index in the CGGA dataset. Furthermore, the ECM index was then validated on three datasets, namely, GSE16011, TCGA-GBM, and GSE83300. The prognosis difference, differentially expressed genes, and potential drugs were obtained. Multiple machine learning methods were selected to construct the model to predict the survival status of GBM patients at 6, 12, 18, 24, 30, and 36 months after diagnosis. Results: Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis. GBM patients were divided into high- and low-ECM index groups with significantly different overall survival rates in four datasets. High-ECM index patients exhibited a worse prognosis than low-ECM index patients. Four small molecules (podophyllotoxin, lasalocid, MG-262, and nystatin) that might reduce GBM development were predicted by the Cmap dataset. In the independent dataset (GSE83300), the maximum values of prediction accuracy at 6, 12, 18, 24, 30, and 36 months were 0.878, 0.769, 0.748, 0.720, 0.705, and 0.868, respectively. These machine learning models were provided on a publicly accessible, open-source website (https://ospg.shinyapps.io/OSPG/). Conclusion: In summary, our findings indicated that ECM genes were prognostic indicators for patient survival. This study provided an online server for the prediction of survival curves of GBM patients.", "claims": [{"id": "claim-method", "statement": "We used a univariate Cox regression analysis in CGGA, GSE16011, and TCGA-GBM to examine the links between ECM gene (1,936 unique ECM-related genes from 47 ECM gene sets) expression and overall survival (OS).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35783254", "locator": "sections[4] \"Construction and Validation of the ECM Index\" paragraph 2", "quote": "We used a univariate Cox regression analysis in CGGA, GSE16011, and TCGA-GBM to examine the links between ECM gene (1,936 unique ECM-related genes from 47 ECM gene sets) expression and overall survival (OS)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35783254", "locator": "sections[20] \"Data Availability Statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35783254", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Five ECM gene signatures (AEBP1, F3, FLNC, IGFBP2, and LDHA) were recognized to be associated with the prognosis.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:35783254"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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