<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(12)</volume><submitter>Guerriero I</submitter><pubmed_abstract>Hyperactivation of the PI3K/AKT pathway is observed in most human cancer including lung carcinomas. Here we have investigated the role of miRNAs as downstream targets of activated PI3K/AKT signaling in Non Small Cell Lung Cancer (NSCLC). To this aim, miRNA profiling was performed in human lung epithelial cells (BEAS-2B) expressing active AKT1 (BEAS-AKT1-E17K), active PI3KCA (BEAS-PIK3CA-E545K) or with silenced PTEN (BEAS-shPTEN).Twenty-four differentially expressed miRNAs common to BEAS-AKT1-E17K, BEAS-PIK3CA-E545K and BEAS-shPTEN cells were identified through this analysis, with miR-196a being the most consistently up-regulated miRNA. Interestingly, miR-196a was significantly overexpressed also in human NSCLC-derived cell lines (n=11) and primary lung cancer samples (n=28).By manipulating</pubmed_abstract><journal>Oncotarget</journal><pagination>19172-19191</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5386676</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Analysis of miRNA profiles identified miR-196a as a crucial mediator of aberrant PI3K/AKT signaling in lung cancer cells.</pubmed_title><pmcid>PMC5386676</pmcid><pubmed_authors>Guerriero I</pubmed_authors><pubmed_authors>Scrima M</pubmed_authors><pubmed_authors>Ceccarelli M</pubmed_authors><pubmed_authors>Santos M</pubmed_authors><pubmed_authors>De Marco C</pubmed_authors><pubmed_authors>Ravo M</pubmed_authors><pubmed_authors>Malanga D</pubmed_authors><pubmed_authors>Rizzuto A</pubmed_authors><pubmed_authors>Pallante P</pubmed_authors><pubmed_authors>Weisz A</pubmed_authors><pubmed_authors>D'Angelo D</pubmed_authors><pubmed_authors>Viglietto G</pubmed_authors><pubmed_authors>Laudanna C</pubmed_authors><pubmed_authors>Falco G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of miRNA profiles identified miR-196a as a crucial mediator of aberrant PI3K/AKT signaling in lung cancer cells.</name><description>Hyperactivation of the PI3K/AKT pathway is observed in most human cancer including lung carcinomas. Here we have investigated the role of miRNAs as downstream targets of activated PI3K/AKT signaling in Non Small Cell Lung Cancer (NSCLC). To this aim, miRNA profiling was performed in human lung epithelial cells (BEAS-2B) expressing active AKT1 (BEAS-AKT1-E17K), active PI3KCA (BEAS-PIK3CA-E545K) or with silenced PTEN (BEAS-shPTEN).Twenty-four differentially expressed miRNAs common to BEAS-AKT1-E17K, BEAS-PIK3CA-E545K and BEAS-shPTEN cells were identified through this analysis, with miR-196a being the most consistently up-regulated miRNA. Interestingly, miR-196a was significantly overexpressed also in human NSCLC-derived cell lines (n=11) and primary lung cancer samples (n=28).By manipulating</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2026-05-30T12:42:24.812Z</modification><creation>2019-03-27T02:40:57Z</creation></dates><accession>S-EPMC5386676</accession><cross_references><pubmed>27880728</pubmed><doi>10.18632/oncotarget.13432</doi></cross_references></HashMap>