<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25</volume><submitter>Hosen MR</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Deutsche Gesellschaft fur Kardiologie - Herz- und Kreislaufforschung eV</funding><funding>Corona Foundation</funding><pubmed_abstract>Long noncoding RNAs (lncRNAs) have emerged as biomarkers and regulators of cardiovascular disease. However, the expression pattern of circulating extracellular vesicle (EV)-incorporated lncRNAs in patients with coronary artery disease (CAD) is still poorly investigated. A human lncRNA array revealed that certain EV-lncRNAs are significantly dysregulated in CAD patients. Circulating small EVs (sEVs) from patients with (n = 30) or without (n = 30) CAD were used to quantify &lt;i>PUNISHER&lt;/i> (also known as &lt;i>AGAP2-&lt;/i>antisense RNA 1 [&lt;i>AS1&lt;/i>]), &lt;i>GAS5&lt;/i>, &lt;i>MALAT1&lt;/i>, and &lt;i>H19&lt;/i> RNA levels. &lt;i>PUNISHER&lt;/i> (p = 0.002) and &lt;i>GAS5&lt;/i> (p = 0.02) were significantly increased in patients with CAD, compared to non-CAD patients. Fluorescent labeling and quantitative real-time PCR of sEV</pubmed_abstract><journal>Molecular therapy. Nucleic acids</journal><pagination>388-405</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8403722</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CAD increases the long noncoding RNA &lt;i>PUNISHER&lt;/i> in small extracellular vesicles and regulates endothelial cell function via vesicular shuttling.</pubmed_title><pmcid>PMC8403722</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Zietzer A</pubmed_authors><pubmed_authors>Goody P</pubmed_authors><pubmed_authors>Uchida S</pubmed_authors><pubmed_authors>Werner N</pubmed_authors><pubmed_authors>Hosen MR</pubmed_authors><pubmed_authors>Jansen F</pubmed_authors><pubmed_authors>Nickenig G</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Latz E</pubmed_authors><pubmed_authors>Maus K</pubmed_authors></additional><is_claimable>false</is_claimable><name>CAD increases the long noncoding RNA &lt;i>PUNISHER&lt;/i> in small extracellular vesicles and regulates endothelial cell function via vesicular shuttling.</name><description>Long noncoding RNAs (lncRNAs) have emerged as biomarkers and regulators of cardiovascular disease. However, the expression pattern of circulating extracellular vesicle (EV)-incorporated lncRNAs in patients with coronary artery disease (CAD) is still poorly investigated. A human lncRNA array revealed that certain EV-lncRNAs are significantly dysregulated in CAD patients. Circulating small EVs (sEVs) from patients with (n = 30) or without (n = 30) CAD were used to quantify &lt;i>PUNISHER&lt;/i> (also known as &lt;i>AGAP2-&lt;/i>antisense RNA 1 [&lt;i>AS1&lt;/i>]), &lt;i>GAS5&lt;/i>, &lt;i>MALAT1&lt;/i>, and &lt;i>H19&lt;/i> RNA levels. &lt;i>PUNISHER&lt;/i> (p = 0.002) and &lt;i>GAS5&lt;/i> (p = 0.02) were significantly increased in patients with CAD, compared to non-CAD patients. Fluorescent labeling and quantitative real-time PCR of sEV</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-19T23:58:42.641Z</modification><creation>2022-02-11T11:19:15.815Z</creation></dates><accession>S-EPMC8403722</accession><cross_references><pubmed>34484864</pubmed><doi>10.1016/j.omtn.2021.05.023</doi></cross_references></HashMap>