<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Arunkumar G</submitter><pubmed_abstract>Long non-coding RNAs (lncRNAs) play an important role in the regulation of key cellular processes in early development and cancer. LncRNA Oip5-as1 facilitates stem cell self-renewal in mouse by sponging mmu-miR-7 and modulating NANOG level, yet its role in cancer is less understood. We analyzed OIP5-AS1 expression in oral tumors and in TCGA datasets. We observed overexpression of OIP5-AS1 in oral tumors (P &lt; 0.001) and in tumors of epithelial origin from TCGA. OIP5-AS1 expression was strongly associated with undifferentiated tumors (P = 0.0038). In silico analysis showed miR-7 binding site is conserved in mouse and human OIP5-AS1. However, human NANOG 3'-UTR lost the binding site for hsa-miR-7a-3. Therefore, we screened for other miRNAs that can be sponged by OIP5-AS1 and identified six po</pubmed_abstract><journal>Scientific reports</journal><pagination>7018</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5935738</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>LncRNA OIP5-AS1 is overexpressed in undifferentiated oral tumors and integrated analysis identifies as a downstream effector of stemness-associated transcription factors.</pubmed_title><pmcid>PMC5935738</pmcid><pubmed_authors>Munirajan AK</pubmed_authors><pubmed_authors>Raksha P</pubmed_authors><pubmed_authors>Murugan AK</pubmed_authors><pubmed_authors>Anand S</pubmed_authors><pubmed_authors>Arunkumar G</pubmed_authors><pubmed_authors>Dhamodharan S</pubmed_authors><pubmed_authors>Subbiah S</pubmed_authors><pubmed_authors>Prasanna Srinivasa Rao H</pubmed_authors></additional><is_claimable>false</is_claimable><name>LncRNA OIP5-AS1 is overexpressed in undifferentiated oral tumors and integrated analysis identifies as a downstream effector of stemness-associated transcription factors.</name><description>Long non-coding RNAs (lncRNAs) play an important role in the regulation of key cellular processes in early development and cancer. LncRNA Oip5-as1 facilitates stem cell self-renewal in mouse by sponging mmu-miR-7 and modulating NANOG level, yet its role in cancer is less understood. We analyzed OIP5-AS1 expression in oral tumors and in TCGA datasets. We observed overexpression of OIP5-AS1 in oral tumors (P &lt; 0.001) and in tumors of epithelial origin from TCGA. OIP5-AS1 expression was strongly associated with undifferentiated tumors (P = 0.0038). In silico analysis showed miR-7 binding site is conserved in mouse and human OIP5-AS1. However, human NANOG 3'-UTR lost the binding site for hsa-miR-7a-3. Therefore, we screened for other miRNAs that can be sponged by OIP5-AS1 and identified six po</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 May</publication><modification>2026-05-05T23:32:43.99Z</modification><creation>2019-03-26T23:36:48Z</creation></dates><accession>S-EPMC5935738</accession><cross_references><pubmed>29728583</pubmed><doi>10.1038/s41598-018-25451-3</doi></cross_references></HashMap>