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pmid:33687057

Mining the key genes for ventilator-induced lung injury using co-expression network analysis.

Zhao Li · Yajun Xiao · Li Xu · Qingxiu Wang

Bioscience reports · 2021 doi:10.1042/BSR20203235

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:33687057
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2026-11-01T15:41:27Z
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2026-11-01T22:46:16Z
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paper object · 10 fields
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title
Mining the key genes for ventilator-induced lung injury using co-expression network analysis.
doi
10.1042/BSR20203235
pmid
33687057
authors array · 4 items
[0]
Zhao Li
[1]
Yajun Xiao
[2]
Li Xu
[3]
Qingxiu Wang
journal
Bioscience reports
year
2021
abstract
Mechanical ventilation is extensively adopted in general anesthesia and respiratory failure management, but it can also induce ventilator-induced lung injury (VILI). Therefore, it is of great urgency to explore the mechanisms involved in the VILI pathogenesis, which might contribute to its future prevention and treatment. Four microarray datasets from the GEO database were selected in our investigation, and were subjected to the Weighted Gene Co-Expression Network Analysis (WGCNA) to identify the VILI-correlated gene modules. The limma package in R software was used to identify the differentially expressed genes (DEGs) between the VILI and control groups. WGCNA was constructed by merging the GSE9314, GSE9368, GSE11434 and GSE11662 datasets. A total of 49 co-expression network modules were determined as associated with VILI. The intersected genes between hub genes screened from DEGs for VILI and those identified using WGCNA were as follows: Tlr2, Hmox1, Serpine1, Mmp9, Il6, Il1b, Ptgs2, Fos and Atf3, which were determined to be key genes for VILI. Those key genes were validated by GSE86229 and quantitative PCR (qPCR) experiment to have significantly statistical difference in their expression between the VILI and control groups. In a nutshell, nine key genes with expression differences in VILI were screened by WGCNA by integrating multiple datasets.
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Differential expression analysis was performed based on the merged expression profiling data, and DEGs were identified using the limma package for R, under the condition of adj P<0.05 and |log2FC|>1.
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sections[6] "Identification of DEGs" paragraph 2
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Differential expression analysis was performed based on the merged expression profiling data, and DEGs were identified using the limma package for R, under the condition of adj P<0.05 and |log2FC|>1.
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The data used and/or analyzed in the present study are available in the GEO database (https://www.ncbi.nlm.nih.gov/geo).
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Ventilator-induced lung injury in C57BL\6 mice
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GADD45a in ventilator-induced lung injury: role of Akt signaling
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Effect of Hypercapnia on Murine Ventilator-Induced Lung Injury
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Mouse lung with recombinant human soluble PBEFtreatment and ventilator-induced lung injury: age 8-12wks
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2026-11-01T15:39:55Z
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to its future prevention and treatment. Four microarray datasets from the GEO database were selected
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sodium pentobarbital (MERCK, Germany). Then mice were anesthetized and subjected to tracheal intub
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Differential expression analysis was performed based on the merged expression profiling data, and DEGs were identified using the limma package for R, under the condition of adj P<0.05 and |log2FC|>1.
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assay:3
Complete file
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Therefore, it is of great urgency to explore the mechanisms involved in the VILI pathogenesis, which might contribute to its future prevention and treatment. Four microarray datasets from the GEO database were selected in our investigation, and were subjected to the Weighted Gene Co-Expression Network Analysis (WGCNA) to identify the VILI-correlated gene modules. The limma package in R software was used to identify the differentially expressed genes (DEGs) between the VILI and control groups. WGCNA was constructed by merging the GSE9314, GSE9368, GSE11434 and GSE11662 datasets. A total of 49 co-expression network modules were determined as associated with VILI. The intersected genes between hub genes screened from DEGs for VILI and those identified using WGCNA were as follows: Tlr2, Hmox1, Serpine1, Mmp9, Il6, Il1b, Ptgs2, Fos and Atf3, which were determined to be key genes for VILI. Those key genes were validated by GSE86229 and quantitative PCR (qPCR) experiment to have significantly statistical difference in their expression between the VILI and control groups. 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Four microarray datasets from the GEO database were selected"], "order_basis": "paper_text_order:378", "id": "assay:1"}, {"role": "data_generation", "definition_id": "animal_model", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["sodium pentobarbital (MERCK, Germany). Then mice were anesthetized and subjected to tracheal intub", "s lasted for 4 h. Nonmechanically ventilated mice were used as controls. 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