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Gene Expression Profiles Analysis Identifies Key Genes for Acute Lung Injury in Patients with Sepsis

Overview
Journal Diagn Pathol
Publisher Biomed Central
Specialty Pathology
Date 2014 Sep 27
PMID 25257390
Citations 4
Authors
Affiliations
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Abstract

Background: To identify critical genes and biological pathways in acute lung injury (ALI), a comparative analysis of gene expression profiles of patients with ALI + sepsis compared with patients with sepsis alone were performed with bioinformatic tools.

Methods: GSE10474 was downloaded from Gene Expression Omnibus, including a collective of 13 whole blood samples with ALI + sepsis and 21 whole blood samples with sepsis alone. After pre-treatment with robust multichip averaging (RMA) method, differential analysis was conducted using simpleaffy package based upon t-test and fold change. Hierarchical clustering was also performed using function hclust from package stats. Beisides, functional enrichment analysis was conducted using iGepros. Moreover, the gene regulatory network was constructed with information from Kyoto Encyclopedia of Genes and Genomes (KEGG) and then visualized by Cytoscape.

Results: A total of 128 differentially expressed genes (DEGs) were identified, including 47 up- and 81 down-regulated genes. The significantly enriched functions included negative regulation of cell proliferation, regulation of response to stimulus and cellular component morphogenesis. A total of 27 DEGs were significantly enriched in 16 KEGG pathways, such as protein digestion and absorption, fatty acid metabolism, amoebiasis, etc. Furthermore, the regulatory network of these 27 DEGs was constructed, which involved several key genes, including protein tyrosine kinase 2 (PTK2), v-src avian sarcoma (SRC) and Caveolin 2 (CAV2).

Conclusion: PTK2, SRC and CAV2 may be potential markers for diagnosis and treatment of ALI.

Virtual Slides: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5865162912987143.

Citing Articles

Identification of Key Metabolites for Acute Lung Injury in Patients with Sepsis.

Wang P, Li J, Zhang L, Lv H, Zhang S Iran J Public Health. 2019; 48(1):77-84.

PMID: 30847314 PMC: 6401565.


Potential mechanism and drug candidates for sepsis-induced acute lung injury.

Xu C, Guo Z, Zhao C, Zhang X, Wang Z Exp Ther Med. 2018; 15(6):4689-4696.

PMID: 29805488 PMC: 5952104. DOI: 10.3892/etm.2018.6001.


Lipid metabolites as potential diagnostic and prognostic biomarkers for acute community acquired pneumonia.

To K, Lee K, Wong S, Sze K, Ke Y, Lui Y Diagn Microbiol Infect Dis. 2016; 85(2):249-54.

PMID: 27105773 PMC: 7173326. DOI: 10.1016/j.diagmicrobio.2016.03.012.


Retraction note: Gene expression profiles analysis identifies key genes for acute lung injury in patients with sepsis.

Diagn Pathol. 2015; 10:51.

PMID: 25967107 PMC: 4429344. DOI: 10.1186/s13000-015-0237-9.

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