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          <dc:title>Immune cell enrichment characteristics and related key genes in intrauterine adhesion: insights from RNA-sequencing analysis</dc:title>
          <dc:creator>Xue Feng (147580)</dc:creator>
          <dc:creator>Lili Yu (149552)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Hematology</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>Immune cell enrichment</dc:subject>
          <dc:subject>key genes</dc:subject>
          <dc:subject>intrauterine adhesion</dc:subject>
          <dc:subject>bioinformatics analysis</dc:subject>
          <dc:description>&lt;p&gt;Intrauterine adhesion (IUA) represents a prevalent cause of persistent infertility and continues to be a significant unresolved challenge in reproductive medicine. However, its full pathogenic mechanisms remain incompletely elucidated. We retrieved endometrial RNA-sequencing data from IUA patients and normal controls in the Gene Expression Omnibus (GEO) database, and screened 586 differentially expressed genes (DEGs) in the endometrium of IUA patients using the R package limma. Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and gene set enrichment analysis (GSEA) revealed activation of immune-related pathways, including chronic inflammatory response, complement activation, and complement and coagulation cascades in IUA. Further single-sample gene set enrichment analysis (ssGSEA)-based relative immune cell enrichment analysis revealed decreased enrichment scores of activated CD4 T cells and type 2 T helper cells, alongside increased enrichment scores of effector memory CD8 T cells, macrophages, mast cells, natural killer cells, and T follicular helper cells in IUA patients, indicating their potential involvement in IUA pathogenesis. A protein–protein interaction (PPI) network was constructed, identifying 10 hub genes associated with IUA: &lt;i&gt;CDK1&lt;/i&gt;, &lt;i&gt;CCNB1&lt;/i&gt;, &lt;i&gt;CCNA2&lt;/i&gt;, &lt;i&gt;CENPA&lt;/i&gt;, &lt;i&gt;BUB1&lt;/i&gt;, &lt;i&gt;AURKB&lt;/i&gt;, &lt;i&gt;KIF11&lt;/i&gt;, &lt;i&gt;BUB1B&lt;/i&gt;, &lt;i&gt;CDC20&lt;/i&gt;, and &lt;i&gt;TOP2A&lt;/i&gt;. The expression patterns of these genes were further validated in two independent external IUA cohorts, supporting a potential correlative link between these genes and IUA pathogenesis. Our findings provide exploratory insights and potential candidate molecules for subsequent mechanistic studies of IUA onset and progression.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-20T17:27:01Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.33945718.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Immune_cell_enrichment_characteristics_and_related_key_genes_in_intrauterine_adhesion_insights_from_RNA-sequencing_analysis/33945718</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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