<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sui S</submitter><funding>Major Science and Technology Program of Changzhou Health Commission in 2020</funding><funding>Project of Changzhou Medical Innovation Team</funding><pagination>10617-10628</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9161985</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(4)</volume><pubmed_abstract>Pancreatic cancer (PC) is a life-threatening cancer with increasing incidence in developed countries. Reports indicate that tRNA-derived fragments (tRFs) are possible therapeutic targets and biomarkers for cancer treatment. Nonetheless, the effect of tRF-Leu-AAG on PC is unclear. This study aims to explore the role of tRF-Leu-AAG and upstream frameshift mutant 1 (UPF1) in the development of PC and its potential underlying mechanisms. High-throughput second-generation sequencing techniques were used to detect the expression of tRFs in cancerous and adjacent normal tissues from PC patients. The role of tRF-Leu-AAG proliferation in PC cells was investigated via the Cell Counting Kit-8 (CCK8) assay. The effect of tRF-Leu-AAG on the invasion and migration ability of PC cells was also determined</pubmed_abstract><journal>Bioengineered</journal><pubmed_title>The biological behavior of tRNA-derived fragment tRF-Leu-AAG in pancreatic cancer cells.</pubmed_title><pmcid>PMC9161985</pmcid><funding_grant_id>ZD202023</funding_grant_id><funding_grant_id>CCX201807</funding_grant_id><pubmed_authors>Sui S</pubmed_authors><pubmed_authors>Cui X</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Jin L</pubmed_authors><pubmed_authors>Zhu C</pubmed_authors></additional><is_claimable>false</is_claimable><name>The biological behavior of tRNA-derived fragment tRF-Leu-AAG in pancreatic cancer cells.</name><description>Pancreatic cancer (PC) is a life-threatening cancer with increasing incidence in developed countries. Reports indicate that tRNA-derived fragments (tRFs) are possible therapeutic targets and biomarkers for cancer treatment. Nonetheless, the effect of tRF-Leu-AAG on PC is unclear. This study aims to explore the role of tRF-Leu-AAG and upstream frameshift mutant 1 (UPF1) in the development of PC and its potential underlying mechanisms. High-throughput second-generation sequencing techniques were used to detect the expression of tRFs in cancerous and adjacent normal tissues from PC patients. The role of tRF-Leu-AAG proliferation in PC cells was investigated via the Cell Counting Kit-8 (CCK8) assay. The effect of tRF-Leu-AAG on the invasion and migration ability of PC cells was also determined</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-22T11:53:33.373Z</modification><creation>2025-04-06T00:05:34.16Z</creation></dates><accession>S-EPMC9161985</accession><cross_references><pubmed>35442152</pubmed><doi>10.1080/21655979.2022.2064206</doi></cross_references></HashMap>