<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kaitsuka T</submitter><funding>Japan Society for the Promotion of Science</funding><pagination>3316</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8699081</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(12)</volume><pubmed_abstract>The sirtuin family of nicotinamide adenine dinucleotide-dependent deacetylase and ADP-ribosyl transferases plays key roles in aging, metabolism, stress response, and aging-related diseases. SIRT2 is a unique sirtuin that is expressed in the cytosol and is abundant in neuronal cells. Various microRNAs were recently reported to regulate SIRT2 expression via its 3'-untranslated region (UTR), and single nucleotide polymorphisms in the miRNA-binding sites of SIRT2 3'-UTR were identified in patients with neurodegenerative diseases. The present review highlights recent studies into SIRT2-mediated regulation of the stress response, posttranscriptional regulation of SIRT2 by microRNAs, and the implications of the SIRT2-miRNA axis in aging-related diseases.</pubmed_abstract><journal>Cells</journal><pubmed_title>Regulation of Hypoxic Signaling and Oxidative Stress via the MicroRNA-SIRT2 Axis and Its Relationship with Aging-Related Diseases.</pubmed_title><pmcid>PMC8699081</pmcid><funding_grant_id>19K07053</funding_grant_id><pubmed_authors>Matsushita N</pubmed_authors><pubmed_authors>Matsushita M</pubmed_authors><pubmed_authors>Kaitsuka T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Regulation of Hypoxic Signaling and Oxidative Stress via the MicroRNA-SIRT2 Axis and Its Relationship with Aging-Related Diseases.</name><description>The sirtuin family of nicotinamide adenine dinucleotide-dependent deacetylase and ADP-ribosyl transferases plays key roles in aging, metabolism, stress response, and aging-related diseases. SIRT2 is a unique sirtuin that is expressed in the cytosol and is abundant in neuronal cells. Various microRNAs were recently reported to regulate SIRT2 expression via its 3'-untranslated region (UTR), and single nucleotide polymorphisms in the miRNA-binding sites of SIRT2 3'-UTR were identified in patients with neurodegenerative diseases. The present review highlights recent studies into SIRT2-mediated regulation of the stress response, posttranscriptional regulation of SIRT2 by microRNAs, and the implications of the SIRT2-miRNA axis in aging-related diseases.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-03T22:46:39.237Z</modification><creation>2022-02-11T14:32:55.295Z</creation></dates><accession>S-EPMC8699081</accession><cross_references><pubmed>34943825</pubmed><doi>10.3390/cells10123316</doi></cross_references></HashMap>