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10.2147/COPD.S333251

http://scihub22266oqcxt.onion/10.2147/COPD.S333251
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suck abstract from ncbi


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pmid35018096      Int+J+Chron+Obstruct+Pulmon+Dis 2022 ; 17 (ä): 13-24
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  • Identification of the Key Immune-Related Genes in Chronic Obstructive Pulmonary Disease Based on Immune Infiltration Analysis #MMPMID35018096
  • Meng H; Long Q; Wang R; Zhou X; Su H; Wang T; Li Y
  • Int J Chron Obstruct Pulmon Dis 2022[]; 17 (ä): 13-24 PMID35018096show ga
  • PURPOSE: Chronic obstructive pulmonary disease (COPD) is a major cause of death and morbidity worldwide. A better understanding of new biomarkers for COPD patients and their complex mechanisms in the progression of COPD are needed. METHODS: An algorithm was conducted to reveal the proportions of 22 subsets of immune cells in COPD samples. Differentially expressed immune-related genes (DE-IRGs) were obtained based on the differentially expressed genes (DEGs) of the GSE57148 dataset, and 1509 immune-related genes (IRGs) were downloaded from the ImmPort database. Functional enrichment analyses of DE-IRGs were conducted by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses and Ingenuity Pathway Analysis (IPA). We defined the DE-IRGs that had correlations with immune cells as hub genes. The potential interactions among the hub genes were explored by a protein-protein interaction (PPI) network. RESULTS: The CIBERSORT results showed that lung tissue of COPD patients contained a greater number of resting NK cells, activated dendritic cells, and neutrophils than normal samples. However, the fractions of follicular helper T cells and resting dendritic cells were relatively lower. Thirty-eight DE-IRGs were obtained for further analysis. Functional enrichment analysis revealed that these DE-IRGs were significantly enriched in several immune-related biological processes and pathways. Notably, we also observed that DE-IRGs were associated with the coronavirus disease COVID-19 in the progression of COPD. After correlation analysis, six DE-IRGs associated with immune cells were considered hub genes, including AHNAK, SLIT2 TNFRRSF10C, CXCR1, CXCR2, and FCGR3B. CONCLUSION: In the present study, we investigated immune-related genes as novel diagnostic biomarkers and explored the potential mechanism for COPD based on CIBERSORT analysis, providing a new understanding for COPD treatment.
  • |*COVID-19[MESH]
  • |*Pulmonary Disease, Chronic Obstructive/diagnosis/genetics[MESH]
  • |Gene Ontology[MESH]
  • |Humans[MESH]
  • |Protein Interaction Maps[MESH]


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