<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Li YY</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Endometrial cancer (EC) is a growing global health concern. Understanding the molecular mechanisms driving EC is crucial for developing effective diagnostic and therapeutic strategies. This study investigates the roles of DLL3 and miR-508-5p in EC progression and explores a therapeutic approach using engineered exosomes to modulate their expression.&lt;h4>Methods&lt;/h4>TCGA data were analyzed, &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> experiments were performed to assess DLL3 and miR-508-5p function, and bioinformatics was used to confirm their interaction. Mesenchymal stem cells (MSCs) were engineered to produce miR-508-5p-overexpressing exosomes, and their therapeutic effects were tested in mouse models.&lt;h4>Results&lt;/h4>Elevated DLL3 and downregulated miR-508-5p were observed in </pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1532564</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11891050</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Engineered exosomes restore miR-508-5p expression in uterine corpus endometrial carcinoma and reduce tumor progression and metastasis by targeting DLL3.</pubmed_title><pmcid>PMC11891050</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Feng JL</pubmed_authors><pubmed_authors>Tian WY</pubmed_authors><pubmed_authors>Du J</pubmed_authors><pubmed_authors>Li YY</pubmed_authors><pubmed_authors>Zhang LP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Engineered exosomes restore miR-508-5p expression in uterine corpus endometrial carcinoma and reduce tumor progression and metastasis by targeting DLL3.</name><description>&lt;h4>Introduction&lt;/h4>Endometrial cancer (EC) is a growing global health concern. Understanding the molecular mechanisms driving EC is crucial for developing effective diagnostic and therapeutic strategies. This study investigates the roles of DLL3 and miR-508-5p in EC progression and explores a therapeutic approach using engineered exosomes to modulate their expression.&lt;h4>Methods&lt;/h4>TCGA data were analyzed, &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> experiments were performed to assess DLL3 and miR-508-5p function, and bioinformatics was used to confirm their interaction. Mesenchymal stem cells (MSCs) were engineered to produce miR-508-5p-overexpressing exosomes, and their therapeutic effects were tested in mouse models.&lt;h4>Results&lt;/h4>Elevated DLL3 and downregulated miR-508-5p were observed in </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-04-04T08:22:15.161Z</modification><creation>2025-04-04T08:22:15.161Z</creation></dates><accession>S-EPMC11891050</accession><cross_references><pubmed>40066092</pubmed><doi>10.3389/fonc.2025.1532564</doi></cross_references></HashMap>