<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2022</volume><submitter>Wang H</submitter><pubmed_abstract>Emerging studies have proved that tRNA-derived fragments (tRFs) play vital roles in tumor metastasis; however, the function of tRFs in gastric cancer (GC) remains largely unclear. We investigated the role of tRF-24-V29K9UV3IU in growth and metastasis of GC using a xenograft mouse model. Differential gene expression downstream of tRF-24-V29K9UV3IU was identified by transcriptome sequencing, and interaction was then verified by a dual luciferase reporter and RNA immunoprecipitation. MKN-45 cells were also used to explore the biological functions of tRF-24-V29K9UV3IU &lt;i>in vitro&lt;/i>. Here, knockdown of tRF-24-V29K9UV3IU promoted tumor growth and metastasis of GC &lt;i>in vivo&lt;/i>. The expression of tRF-24-V29K9UV3IU and E-cadherin (epithelial cell marker) was down-regulated in tumors of mice fol</pubmed_abstract><journal>Journal of oncology</journal><pagination>8777697</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9077451</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The tRNA-Derived Fragment tRF-24-V29K9UV3IU Functions as a miRNA-like RNA to Prevent Gastric Cancer Progression by Inhibiting GPR78 Expression.</pubmed_title><pmcid>PMC9077451</pmcid><pubmed_authors>Fan X</pubmed_authors><pubmed_authors>Yu S</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Chen S</pubmed_authors></additional><is_claimable>false</is_claimable><name>The tRNA-Derived Fragment tRF-24-V29K9UV3IU Functions as a miRNA-like RNA to Prevent Gastric Cancer Progression by Inhibiting GPR78 Expression.</name><description>Emerging studies have proved that tRNA-derived fragments (tRFs) play vital roles in tumor metastasis; however, the function of tRFs in gastric cancer (GC) remains largely unclear. We investigated the role of tRF-24-V29K9UV3IU in growth and metastasis of GC using a xenograft mouse model. Differential gene expression downstream of tRF-24-V29K9UV3IU was identified by transcriptome sequencing, and interaction was then verified by a dual luciferase reporter and RNA immunoprecipitation. MKN-45 cells were also used to explore the biological functions of tRF-24-V29K9UV3IU &lt;i>in vitro&lt;/i>. Here, knockdown of tRF-24-V29K9UV3IU promoted tumor growth and metastasis of GC &lt;i>in vivo&lt;/i>. The expression of tRF-24-V29K9UV3IU and E-cadherin (epithelial cell marker) was down-regulated in tumors of mice fol</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T09:10:24.535Z</modification><creation>2025-02-19T03:27:16.113Z</creation></dates><accession>S-EPMC9077451</accession><cross_references><pubmed>35535309</pubmed><doi>10.1155/2022/8777697</doi></cross_references></HashMap>