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pmid:38540240
Immune Gene Networks from Lung Cancer Patients Treated with Immune Checkpoint Inhibitors.
Kyung Soo Kim · Taewon Kang · Dong Wook Jekarl
Biomedicines · 2024 doi:10.3390/biomedicines12030628
Paper
complete
Experiment
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Data
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Analysis
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Execution
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Complete file
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Datasets with more than 10 samples of normal control and tumor tissues were selected; of these, GSE87340, GSE120622, and GSE111907 were suitable for analysis. Gene set enrichment for pathway analysis was performed. For immune gene network construction, 998 unique immune genes were selected from 21 pathways in the Kyoto Encyclopedia of Genes and Genomes (KEGG). Gene function annotation was performed based on the KEGG, Gene Ontology, and Reactome databases. Tumor tissues showed decreased coagulation, hematopoiesis, and innate immune pathways, whereas complement- and coagulation-related genes were prominent in the tumor immune gene network. The average numbers of neighbors, clustering coefficients, network diameters, path lengths, densities, and heterogeneities were highest for normal tissue, followed by LUAD and LUSC. Decreased coagulation genes, which were prominent in tumor immune networks, imply functional attenuation. 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