<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(6)</volume><submitter>Liu L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Studying the mechanism of action of LncRNAs in lung adenocarcinoma (LUAD) is of great importance for an in-depth understanding of the molecular mechanism of lung adeno carcinogenesis and development.&lt;h4>Objective&lt;/h4>The aim is to identify a long non-coding RNA LINC01117 that is specifically and highly expressed in LUAD cells and to investigate its biological functions and molecular mechanisms in LUAD cells, providing a new potential target for targeting LUAD therapy.&lt;h4>Methods&lt;/h4>This study used publicly available data downloaded from The Cancer Genome Atlas (TCGA) database. Construction of siRNA and overexpression plasmid-packed lentiviral constructs were used to knock down and increase the expression of LINC01117 in LUAD cells. The effect of LINC01117 on LUAD cell m</pubmed_abstract><journal>PloS one</journal><pagination>e0287926</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10310029</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>LINC01117 inhibits invasion and migration of lung adenocarcinoma through influencing EMT process.</pubmed_title><pmcid>PMC10310029</pmcid><pubmed_authors>Ren W</pubmed_authors><pubmed_authors>Xu K</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Du L</pubmed_authors></additional><is_claimable>false</is_claimable><name>LINC01117 inhibits invasion and migration of lung adenocarcinoma through influencing EMT process.</name><description>&lt;h4>Background&lt;/h4>Studying the mechanism of action of LncRNAs in lung adenocarcinoma (LUAD) is of great importance for an in-depth understanding of the molecular mechanism of lung adeno carcinogenesis and development.&lt;h4>Objective&lt;/h4>The aim is to identify a long non-coding RNA LINC01117 that is specifically and highly expressed in LUAD cells and to investigate its biological functions and molecular mechanisms in LUAD cells, providing a new potential target for targeting LUAD therapy.&lt;h4>Methods&lt;/h4>This study used publicly available data downloaded from The Cancer Genome Atlas (TCGA) database. Construction of siRNA and overexpression plasmid-packed lentiviral constructs were used to knock down and increase the expression of LINC01117 in LUAD cells. The effect of LINC01117 on LUAD cell m</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T14:08:18.289Z</modification><creation>2025-04-04T14:08:18.289Z</creation></dates><accession>S-EPMC10310029</accession><cross_references><pubmed>37384755</pubmed><doi>10.1371/journal.pone.0287926</doi></cross_references></HashMap>