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ABSTRACT: Background
This study aims to evaluate novel immune-related biomarkers for distinguishing borderline ovarian tumors (BOTs) from Benign ovarian tumors (BeOTs), addressing the diagnostic challenges posed by their intermediate biological behavior between benign and malignant neoplasms.Methods
We obtained the microarray expression profiles from the datasets (GSE4122 + GSE6822 + GSE36668) in the Gene Expression Omnibus (GEO) database and integrated them with the immune-related genes in the ImmPort database. Differentially immune-related genes (DIRGs) underwent Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Protein-protein interaction (PPI) network was built to explore the connection. Candidate biomarkers were identified using the Least
SUBMITTER: Chen S
PROVIDER: S-EPMC12434131 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature