<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Deng X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Esophageal cancer (EC) has a high incidence and is highly invasive. It is meaningful to employ invasion-related genes (IRGs) to predict patients' prognosis.&lt;h4>Methods&lt;/h4>We launched a weighted correlation network analysis to screen for EC tumor differentially expressed IRGs (module genes) from the TCGA-ESCA dataset. By executing univariate-LASSO-multivariate Cox regression analyses, we stepwise selected module genes to obtain prognostic feature genes and create a model. We validated the model using the external GEO dataset GSE53624. We assessed the model's independent prognosis prediction ability. A nomogram was plotted and further validated later. GSEA was undertaken on high-risk groups (Group H). We compared immunity and tumor mutations in Group H and the low-risk gr</pubmed_abstract><journal>Discover oncology</journal><pagination>1695</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12460863</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Selection of tumor invasion-related genes to build a prognostic model and predict immune response and potential drugs for esophageal cancer patients based on WGCNA.</pubmed_title><pmcid>PMC12460863</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Deng X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Selection of tumor invasion-related genes to build a prognostic model and predict immune response and potential drugs for esophageal cancer patients based on WGCNA.</name><description>&lt;h4>Background&lt;/h4>Esophageal cancer (EC) has a high incidence and is highly invasive. It is meaningful to employ invasion-related genes (IRGs) to predict patients' prognosis.&lt;h4>Methods&lt;/h4>We launched a weighted correlation network analysis to screen for EC tumor differentially expressed IRGs (module genes) from the TCGA-ESCA dataset. By executing univariate-LASSO-multivariate Cox regression analyses, we stepwise selected module genes to obtain prognostic feature genes and create a model. We validated the model using the external GEO dataset GSE53624. We assessed the model's independent prognosis prediction ability. A nomogram was plotted and further validated later. GSEA was undertaken on high-risk groups (Group H). We compared immunity and tumor mutations in Group H and the low-risk gr</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-31T03:10:37.86Z</modification><creation>2026-05-31T03:07:17.599Z</creation></dates><accession>S-EPMC12460863</accession><cross_references><pubmed>40991071</pubmed><doi>10.1007/s12672-025-03095-w</doi></cross_references></HashMap>