<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Feng S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Aging-related genes (ARGs) are prognostic markers in cancers, but their role in lung adenocarcinoma (LUAD) remains unclear. Investigating ARGs in LUAD may provide valuable insights for clinical diagnosis and treatment.&lt;h4>Methods&lt;/h4>Gene expression profiles from TCGA and GEO datasets were analyzed to identify ARG-related genes. Univariate Cox regression and LASSO analysis were used to construct a prognostic risk model. Kaplan-Meier survival analysis, ROC curves, and clinicopathological features validated its predictive accuracy. Immune cell infiltration and tumor microenvironment were assessed using CIBERSORT and ESTIMATE. RT-qPCR was used to validate the differential expression of key genes in LUAD and adjacent normal tissues.&lt;h4>Results&lt;/h4>Seven prognostic ARGs (RHPN</pubmed_abstract><journal>Discover oncology</journal><pagination>2293</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12748445</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Mendelian randomization-based risk model using aging-related genes for prognosis in lung adenocarcinoma.</pubmed_title><pmcid>PMC12748445</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Cai J</pubmed_authors><pubmed_authors>Feng S</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Mendelian randomization-based risk model using aging-related genes for prognosis in lung adenocarcinoma.</name><description>&lt;h4>Background&lt;/h4>Aging-related genes (ARGs) are prognostic markers in cancers, but their role in lung adenocarcinoma (LUAD) remains unclear. Investigating ARGs in LUAD may provide valuable insights for clinical diagnosis and treatment.&lt;h4>Methods&lt;/h4>Gene expression profiles from TCGA and GEO datasets were analyzed to identify ARG-related genes. Univariate Cox regression and LASSO analysis were used to construct a prognostic risk model. Kaplan-Meier survival analysis, ROC curves, and clinicopathological features validated its predictive accuracy. Immune cell infiltration and tumor microenvironment were assessed using CIBERSORT and ESTIMATE. RT-qPCR was used to validate the differential expression of key genes in LUAD and adjacent normal tissues.&lt;h4>Results&lt;/h4>Seven prognostic ARGs (RHPN</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-06T09:39:36.641Z</modification><creation>2026-05-28T03:12:00.033Z</creation></dates><accession>S-EPMC12748445</accession><cross_references><pubmed>41284116</pubmed><doi>10.1007/s12672-025-04101-x</doi></cross_references></HashMap>