<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shi T</submitter><funding>Collaborative custom development of RNA probes</funding><pagination>2268</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12467871</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(9)</volume><pubmed_abstract>&lt;b>Background/Objectives:&lt;/b> Gastric cancer (GC), a prevalent global malignancy and a leading cause of cancer-related mortality, has a poorly understood prognosis related to &lt;i>TRIP13&lt;/i> expression. &lt;i>TRIP13&lt;/i> has a recognized part in driving tumor progression across different cancer types, yet its precise role in GC remains beyond our full comprehension. Our study aimed to explore &lt;i>TRIP13's&lt;/i> prognostic value and function in GC patients. &lt;b>Methods&lt;/b>: We extensively explored &lt;i>TRIP13's&lt;/i> influence on GC prognosis, functionality, and immune response by examining various cancer-related databases like UALCAN, GEPIA, GEO, and TIMER. Immunohistochemistry (IHC) staining was also conducted to assess the link between &lt;i>TRIM13&lt;/i> and GC patient survival. &lt;b>Results&lt;/b>: &lt;i>TRIP13&lt;/</pubmed_abstract><journal>Biomedicines</journal><pubmed_title>Decoding TRIP13's Role in Gastric Cancer: Implications for Prognosis and Immune Response.</pubmed_title><pmcid>PMC12467871</pmcid><funding_grant_id>P112213323</funding_grant_id><pubmed_authors>Zhao A</pubmed_authors><pubmed_authors>Chen F</pubmed_authors><pubmed_authors>Shi T</pubmed_authors><pubmed_authors>Xia S</pubmed_authors><pubmed_authors>Shen Y</pubmed_authors><pubmed_authors>Dong R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Decoding TRIP13's Role in Gastric Cancer: Implications for Prognosis and Immune Response.</name><description>&lt;b>Background/Objectives:&lt;/b> Gastric cancer (GC), a prevalent global malignancy and a leading cause of cancer-related mortality, has a poorly understood prognosis related to &lt;i>TRIP13&lt;/i> expression. &lt;i>TRIP13&lt;/i> has a recognized part in driving tumor progression across different cancer types, yet its precise role in GC remains beyond our full comprehension. Our study aimed to explore &lt;i>TRIP13's&lt;/i> prognostic value and function in GC patients. &lt;b>Methods&lt;/b>: We extensively explored &lt;i>TRIP13's&lt;/i> influence on GC prognosis, functionality, and immune response by examining various cancer-related databases like UALCAN, GEPIA, GEO, and TIMER. Immunohistochemistry (IHC) staining was also conducted to assess the link between &lt;i>TRIM13&lt;/i> and GC patient survival. &lt;b>Results&lt;/b>: &lt;i>TRIP13&lt;/</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-30T03:24:11.858Z</modification><creation>2026-06-30T03:16:37.791Z</creation></dates><accession>S-EPMC12467871</accession><cross_references><pubmed>41007830</pubmed><doi>10.3390/biomedicines13092268</doi></cross_references></HashMap>