<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>104(46)</volume><submitter>Ma Y</submitter><pubmed_abstract>Lung adenocarcinoma (LUAD), a common type of non-small cell lung cancer, is associated with low survival rates and challenges in early detection. Therefore, identifying prognostic biomarkers is crucial for improving patient outcomes. This study utilized 2 datasets - the Cancer Genome Atlas-Lung Adenocarcinoma (TCGA-LUAD) and GSE72094 - along with 182 immune escape-related genes and 597 cancer-associated fibroblast-related genes. Weighted gene co-expression network analysis was used to identify module genes. Differential expression analysis of TCGA-LUAD data revealed LUAD-associated differentially expressed genes, which were then intersected with module genes to identify LUAD-specific differentially expressed immune escape-cancer fibroblast-related genes. To identify potential biomarkers an</pubmed_abstract><journal>Medicine</journal><pagination>e45756</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12622665</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification and validation of a diagnostic and prognostic model based on immune escape and cancer-associated fibroblast-related genes in lung adenocarcinoma.</pubmed_title><pmcid>PMC12622665</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Geng R</pubmed_authors><pubmed_authors>Song B</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Hao Y</pubmed_authors><pubmed_authors>Su W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification and validation of a diagnostic and prognostic model based on immune escape and cancer-associated fibroblast-related genes in lung adenocarcinoma.</name><description>Lung adenocarcinoma (LUAD), a common type of non-small cell lung cancer, is associated with low survival rates and challenges in early detection. Therefore, identifying prognostic biomarkers is crucial for improving patient outcomes. This study utilized 2 datasets - the Cancer Genome Atlas-Lung Adenocarcinoma (TCGA-LUAD) and GSE72094 - along with 182 immune escape-related genes and 597 cancer-associated fibroblast-related genes. Weighted gene co-expression network analysis was used to identify module genes. Differential expression analysis of TCGA-LUAD data revealed LUAD-associated differentially expressed genes, which were then intersected with module genes to identify LUAD-specific differentially expressed immune escape-cancer fibroblast-related genes. To identify potential biomarkers an</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T16:36:15.585Z</modification><creation>2026-05-18T03:13:18.699Z</creation></dates><accession>S-EPMC12622665</accession><cross_references><pubmed>41239716</pubmed><doi>10.1097/MD.0000000000045756</doi></cross_references></HashMap>