<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(2)</volume><submitter>Hu YJ</submitter><pubmed_abstract>A better understanding of the molecular mechanism involving the lncRNA-miRNA-mRNA network underlying radiation damage can be beneficial for radioprotection. This study was designed to investigate the potential role of lncRNA NEAT1, miR-147 and Phosphoinositide Dependent Protein Kinase 1 (PDPK1) interaction in radioprotection by troxerutin (TRT). We first demonstrated that NEAT1 sponged miR-147, and PDPK1 mRNA was the primary target of miR-147. In the cells, the NEAT1 and PDPK1 levels were downregulated after the radiation but increased after the treatment with TRT. The miR-147 level was significantly induced by radiation and inhibited by TRT. NEAT1 negatively regulated the expression of miR-147, whereas miR-47 targeted PDPK1 to downregulate its expression. In radioprotection, TRT effective</pubmed_abstract><journal>iScience</journal><pagination>105932</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9868541</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Activation of long-non-coding RNA NEAT1 sponging microRNA-147 inhibits radiation damage by targeting PDPK1 in troxerutin radioprotection.</pubmed_title><pmcid>PMC9868541</pmcid><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Wang TY</pubmed_authors><pubmed_authors>Xu P</pubmed_authors><pubmed_authors>Hu YJ</pubmed_authors><pubmed_authors>Dou WT</pubmed_authors><pubmed_authors>Zhang N</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Yan YD</pubmed_authors><pubmed_authors>Li YF</pubmed_authors><pubmed_authors>Cheng CY</pubmed_authors><pubmed_authors>Song GY</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang JL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Activation of long-non-coding RNA NEAT1 sponging microRNA-147 inhibits radiation damage by targeting PDPK1 in troxerutin radioprotection.</name><description>A better understanding of the molecular mechanism involving the lncRNA-miRNA-mRNA network underlying radiation damage can be beneficial for radioprotection. This study was designed to investigate the potential role of lncRNA NEAT1, miR-147 and Phosphoinositide Dependent Protein Kinase 1 (PDPK1) interaction in radioprotection by troxerutin (TRT). We first demonstrated that NEAT1 sponged miR-147, and PDPK1 mRNA was the primary target of miR-147. In the cells, the NEAT1 and PDPK1 levels were downregulated after the radiation but increased after the treatment with TRT. The miR-147 level was significantly induced by radiation and inhibited by TRT. NEAT1 negatively regulated the expression of miR-147, whereas miR-47 targeted PDPK1 to downregulate its expression. In radioprotection, TRT effective</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-07-14T15:40:50.207Z</modification><creation>2025-04-05T21:46:26.621Z</creation></dates><accession>S-EPMC9868541</accession><cross_references><pubmed>36698722</pubmed><doi>10.1016/j.isci.2023.105932</doi></cross_references></HashMap>