<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Reichelt-Wurm S</submitter><funding>Universitätsklinikum Regensburg</funding><pubmed_abstract>The hypoxia-inducible factor 1α (Hif1α) represents the master transcription factor coordinating cellular responses to oxygen depletion. With hundreds of target genes it plays a key role in numerous bio-medical conditions as well as neoplastic and non-cancerous diseases, which in turn requires a strict regulation. Long non-coding RNAs have the potential to virtually control every step of gene expression. We aimed to investigate the expression and role of HIF1A antisense lncRNAs HIF1A-AS1, AS2, and AS3 under hyperglycemic, hypoxic, or both conditions in three non-cancerous human renal cell types: HK-2 cells, primary RPTECs, and mesangial cells. We observed that HIF1A-AS2 and AS3 expression was upregulated under oxygen deprivation. Furthermore, knockdown (KD) of HIF1A-AS3 resulted in a signif</pubmed_abstract><journal>Scientific reports</journal><pagination>27876</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12310967</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cell-type specific effects of the long non-coding RNA HIF1A-AS3 on HIF1A expression in kidney cells.</pubmed_title><pmcid>PMC12310967</pmcid><pubmed_authors>Kretz M</pubmed_authors><pubmed_authors>Reichelt-Wurm S</pubmed_authors><pubmed_authors>Knauss L</pubmed_authors><pubmed_authors>Eggenhofer E</pubmed_authors><pubmed_authors>Scharf M</pubmed_authors><pubmed_authors>Strasser B</pubmed_authors><pubmed_authors>Holler K</pubmed_authors><pubmed_authors>Banas B</pubmed_authors><pubmed_authors>Banas MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cell-type specific effects of the long non-coding RNA HIF1A-AS3 on HIF1A expression in kidney cells.</name><description>The hypoxia-inducible factor 1α (Hif1α) represents the master transcription factor coordinating cellular responses to oxygen depletion. With hundreds of target genes it plays a key role in numerous bio-medical conditions as well as neoplastic and non-cancerous diseases, which in turn requires a strict regulation. Long non-coding RNAs have the potential to virtually control every step of gene expression. We aimed to investigate the expression and role of HIF1A antisense lncRNAs HIF1A-AS1, AS2, and AS3 under hyperglycemic, hypoxic, or both conditions in three non-cancerous human renal cell types: HK-2 cells, primary RPTECs, and mesangial cells. We observed that HIF1A-AS2 and AS3 expression was upregulated under oxygen deprivation. Furthermore, knockdown (KD) of HIF1A-AS3 resulted in a signif</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-07-15T09:43:49.61Z</modification><creation>2025-08-16T03:07:07.942Z</creation></dates><accession>S-EPMC12310967</accession><cross_references><pubmed>40739162</pubmed><doi>10.1038/s41598-025-12441-5</doi></cross_references></HashMap>