<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(1)</volume><submitter>Prinz F</submitter><funding>Austrian Science Fund FWF</funding><pubmed_abstract>The microRNA-200 family has wide-ranging regulatory functions in cancer development and progression. Above all, it is strongly associated with the epithelial-to-mesenchymal transition (EMT), a process during which cells change their epithelial to a mesenchymal phenotype and acquire invasive characteristics. More recently, miR-200 family members have also been reported to impact the immune evasion of cancer cells by regulating the expression of immunoinhibitory immune checkpoints (ICs) like PD-L1. Therefore, we aimed to comprehensively characterize this miR-200 family as a regulatory interface between EMT and immune evasion mechanisms in biliary tract cancer. Initial correlation analyses and transient overexpression experiments using miRNA mimics suggested miR-200c-3p as a putative regulato</pubmed_abstract><journal>RNA biology</journal><pagination>1305-1315</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9728468</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MicroRNA mimics can distort physiological microRNA effects on immune checkpoints by triggering an antiviral interferon response.</pubmed_title><pmcid>PMC9728468</pmcid><pubmed_authors>Reicher A</pubmed_authors><pubmed_authors>Mayr C</pubmed_authors><pubmed_authors>Rinner B</pubmed_authors><pubmed_authors>Balihodzic A</pubmed_authors><pubmed_authors>Pichler M</pubmed_authors><pubmed_authors>Kiesslich T</pubmed_authors><pubmed_authors>Riedl J</pubmed_authors><pubmed_authors>Gerger A</pubmed_authors><pubmed_authors>Prinz F</pubmed_authors><pubmed_authors>Barth DA</pubmed_authors><pubmed_authors>Jonas K</pubmed_authors><pubmed_authors>Kargl J</pubmed_authors><pubmed_authors>Klec C</pubmed_authors></additional><is_claimable>false</is_claimable><name>MicroRNA mimics can distort physiological microRNA effects on immune checkpoints by triggering an antiviral interferon response.</name><description>The microRNA-200 family has wide-ranging regulatory functions in cancer development and progression. Above all, it is strongly associated with the epithelial-to-mesenchymal transition (EMT), a process during which cells change their epithelial to a mesenchymal phenotype and acquire invasive characteristics. More recently, miR-200 family members have also been reported to impact the immune evasion of cancer cells by regulating the expression of immunoinhibitory immune checkpoints (ICs) like PD-L1. Therefore, we aimed to comprehensively characterize this miR-200 family as a regulatory interface between EMT and immune evasion mechanisms in biliary tract cancer. Initial correlation analyses and transient overexpression experiments using miRNA mimics suggested miR-200c-3p as a putative regulato</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-22T11:22:44.012Z</modification><creation>2025-04-05T23:54:22.241Z</creation></dates><accession>S-EPMC9728468</accession><cross_references><pubmed>36469564</pubmed><doi>10.1080/15476286.2022.2152978</doi></cross_references></HashMap>