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pmid:37593462

Hub genes identification and association of key pathways with hypoxia in cancer cells: A bioinformatics analysis.

Faiza Aziz · Naila Shoaib · Abdul Rehman

Saudi journal of biological sciences · 2023 doi:10.1016/j.sjbs.2023.103752

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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title
Hub genes identification and association of key pathways with hypoxia in cancer cells: A bioinformatics analysis.
doi
10.1016/j.sjbs.2023.103752
pmid
37593462
authors array · 3 items
[0]
Faiza Aziz
[1]
Naila Shoaib
[2]
Abdul Rehman
journal
Saudi journal of biological sciences
year
2023
abstract
Three human cancer cell lines (A549, HCT116, and HeLa) were used to investigate the molecular mechanisms and potential prognostic biomarkers associated with hypoxia. We obtained gene expression data from Gene Expression Omnibus (GEO) datasets GSE11704, GSE147384, and GSE38061, which included 5 hypoxic and 8 control samples. Using the GEO2R tool and Venn diagram software, we identified common differentially expressed genes (cDEGs). The cDEGs were then subjected to Gene ontology (GO) and Kyoto Encyclopedia of Gene and Genome (KEGG) pathway analysis by employing DAVID. The hub genes were identified from critical PPI subnetworks through CytoHuba plugin and these genes' prognostic significance and expression were verified using Kaplan-Meier analysis and Gene Expression Profiling Interactive Analysis (GEPIA), respectively. The research showed 676 common DEGs (cDEGs), with 207 upregulated and 469 downregulated genes. The STRING analysis showed 673 nodes and 1446 edges in the PPI network. We identified 4 significant modules and 19 downregulated hub genes. GO analysis revealed all of them were majorly involved in ribosomal large subunit assembly and biogenesis, rRNA processing, ribosome biogenesis, translation, RNA & protein binding frequently at the sites of nucleolus and nucleoplasm while 11 were significantly associated with a better prognosis of hypoxic tumors. Our research sheds light on the molecular mechanisms that underpin hypoxia in human cancer cell lines and identifies potential prognostic biomarkers for hypoxic tumors.
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The expression profiles of GSE11704, GSE147384, and GSE38061 were subsequently retrieved from the GEO database for investigation.
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The research showed 676 common DEGs (cDEGs), with 207 upregulated and 469 downregulated genes.
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Canis lupus familiaris; Mustela putorius furo
title
Absence of host innate immune responses in SARS-CoV-infected ferrets upon subsequent challenge
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MR Imaging Distinguishes Tumor Hypoxia Levels of Different Prognostic and Biological Significance in Cervical Cancer
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