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pmid:40736401

New Diagnostic and Therapeutic Targets for Spinal Cord Injury: GRN Gene.

Han Ding · Lei Feng · Jianping Zhang · Tuo Fang · Jun Shang · Ke Fang · Shiqing Feng

Journal of cellular and molecular medicine · 2025 doi:10.1111/jcmm.70749

Paper

complete

Experiment

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Data

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Analysis

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title
New Diagnostic and Therapeutic Targets for Spinal Cord Injury: GRN Gene.
doi
10.1111/jcmm.70749
pmid
40736401
authors array · 7 items
[0]
Han Ding
[1]
Lei Feng
[2]
Jianping Zhang
[3]
Tuo Fang
[4]
Jun Shang
[5]
Ke Fang
[6]
Shiqing Feng
journal
Journal of cellular and molecular medicine
year
2025
abstract
Spinal cord injury (SCI) is a severe disabling disease due to the poor self-healing of the central nervous system. Studies showed that many N6-methyladenosine (m6A) RNA methylation profiles are hypomethylated after SCI, which are related to neural regeneration and different m6A marker genes. In addition, immune cell infiltration may significantly affect the development and progression of SCI. Therefore, we attempted to identify the correlation between SCI-related biomarkers and m6A methylation regulators in order to classify them. To this end, we collected two gene expression profile datasets (GSE464 and GSE45006) from the GEO database, performed differential expression analysis between pairs before and after SCI, and identified 19 constant differentially expressed genes (DEGs). We found that the constant differential genes were strongly correlated with m6A methylation regulators, which could modulate the immune microenvironment of SCI. Next, this paper used a consensus clustering algorithm to classify SCI patients into three subtypes. There are significant differences between 19 constant DEGs and 28 immune cells among different subtypes. Finally, the correlation analysis of the intersection genes between constant DEGs and immune genes was performed, and GRN was identified as a potential immune biomarker for SCI.
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In this study, the limma package in R [17] was used to perform differential expression analysis on the combined microarray datasets and set at p value less than 0.05 to obtain DEGs of different time points (1 day, 14 days and week > 4).
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sections[5] "Identification of Differentially Expressed Genes" paragraph 2
quote
In this study, the limma package in R [17] was used to perform differential expression analysis on the combined microarray datasets and set at p value less than 0.05 to obtain DEGs of different time points (1 day, 14 days and week > 4).
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sections[30] "Data Availability Statement" paragraph 2
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The data that support the findings of this study are available in GEO database (https://www.ncbi.nlm.nih.gov/geo/).
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GRN was identified as a potential immunobiological marker for SCI, with an AUC of 0.665 for predicting the occurrence of SCI and 0.667 for predicting the degree of injury.
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sections[19] "Identification of Potential Immunobiological Markers of SCI Severity" paragraph 2
quote
The GSE151371 dataset showed that the expression of GRN in the peripheral blood of SCI patients was significantly higher than that of normal samples (Figure 6B), and its expression was correlated with the age of patients (Figure 6C) and low expression in elderly patients, but not with gender (Figure 6D).
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sections[19] "Identification of Potential Immunobiological Markers of SCI Severity" paragraph 2
quote
Among them, the AUC for predicting the occurrence of SCI was 0.665. The AUC for predicting the degree of injury was 0.667. This means that GRN has specific predictive efficacy.
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GRN was identified as a potential immunobiological marker for SCI, with an AUC of 0.665 for predicting the occurrence of SCI and 0.667 for predicting the degree of injury.
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Rattus norvegicus
title
CNS Regeneration
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2026-11-01T20:16:08Z
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identifier_resolution_only_no_download_no_licence_read
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In this study, the limma package in R [17] was used to perform differential expression analysis on the combined microarray datasets and set at p value less than 0.05 to obtain DEGs of different time points (1 day, 14 days and week > 4).
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Automated Assays Laravel application and simulated adapters
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tier
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The data that support the findings of this study are available in GEO database (https://www.ncbi.nlm.nih.gov/geo/).
basis
The paper names GSE464, GSE45006, GSE151371 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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minimax
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single_reader
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In this study, the limma package in R [17] was used to perform differential expression analysis on the combined microarray datasets and set at p value less than 0.05 to obtain DEGs of different time points (1 day, 14 days and week > 4).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40736401", "kind": "science-record", "revision": 4, "content_hash": "sha256:efbc6036564709ed18dfb60a58f82fc284d822034cf6ab7688258e3a8f0d03c2", "created_at": "2026-11-01T20:30:50Z", "updated_at": "2026-11-01T22:56:55Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "New Diagnostic and Therapeutic Targets for Spinal Cord Injury: GRN Gene.", "doi": "10.1111/jcmm.70749", "pmid": "40736401", "authors": ["Han Ding", "Lei Feng", "Jianping Zhang", "Tuo Fang", "Jun Shang", "Ke Fang", "Shiqing Feng"], "journal": "Journal of cellular and molecular medicine", "year": 2025, "abstract": "Spinal cord injury (SCI) is a severe disabling disease due to the poor self-healing of the central nervous system. Studies showed that many N6-methyladenosine (m6A) RNA methylation profiles are hypomethylated after SCI, which are related to neural regeneration and different m6A marker genes. In addition, immune cell infiltration may significantly affect the development and progression of SCI. Therefore, we attempted to identify the correlation between SCI-related biomarkers and m6A methylation regulators in order to classify them. To this end, we collected two gene expression profile datasets (GSE464 and GSE45006) from the GEO database, performed differential expression analysis between pairs before and after SCI, and identified 19 constant differentially expressed genes (DEGs). We found that the constant differential genes were strongly correlated with m6A methylation regulators, which could modulate the immune microenvironment of SCI. Next, this paper used a consensus clustering algorithm to classify SCI patients into three subtypes. There are significant differences between 19 constant DEGs and 28 immune cells among different subtypes. Finally, the correlation analysis of the intersection genes between constant DEGs and immune genes was performed, and GRN was identified as a potential immune biomarker for SCI.", "claims": [{"id": "claim-method", "statement": "In this study, the limma package in R [17] was used to perform differential expression analysis on the combined microarray datasets and set at p value less than 0.05 to obtain DEGs of different time points (1 day, 14 days and week > 4).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40736401", "locator": "sections[5] \"Identification of Differentially Expressed Genes\" paragraph 2", "quote": "In this study, the limma package in R [17] was used to perform differential expression analysis on the combined microarray datasets and set at p value less than 0.05 to obtain DEGs of different time points (1 day, 14 days and week > 4)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data that support the findings of this study are available in GEO database (https://www.ncbi.nlm.nih.gov/geo/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40736401", "locator": "sections[30] \"Data Availability Statement\" paragraph 2", "quote": "The data that support the findings of this study are available in GEO database (https://www.ncbi.nlm.nih.gov/geo/)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "GRN was identified as a potential immunobiological marker for SCI, with an AUC of 0.665 for predicting the occurrence of SCI and 0.667 for predicting the degree of injury.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:40736401", "locator": "sections[19] \"Identification of Potential Immunobiological Markers of SCI Severity\" paragraph 2", "quote": "The GSE151371 dataset showed that the expression of GRN in the peripheral blood of SCI patients was significantly higher than that of normal samples (Figure 6B), and its expression was correlated with the age of patients (Figure 6C) and low expression in elderly patients, but not with gender (Figure 6D)."}, {"asset": "source:pmid:40736401", "locator": "sections[19] \"Identification of Potential Immunobiological Markers of SCI Severity\" paragraph 2", "quote": "Among them, the AUC for predicting the occurrence of SCI was 0.665. The AUC for predicting the degree of injury was 0.667. This means that GRN has specific predictive efficacy."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "GRN was identified as a potential immunobiological marker for SCI, with an AUC of 0.665 for predicting the occurrence of SCI and 0.667 for predicting the degree of injury.", "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:40736401"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE151371"], "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:GSE151371"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:40736401", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1111/jcmm.70749", "sha256": 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