<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Li M</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>There has been no explanation for the exact mechanism of circRNAs in nasopharyngeal carcinoma (NPC). Circ_0007439 was investigated in this study to determine its role and mechanism in NPC.&lt;h4>Methods&lt;/h4>To identify circ_0007439, microRNA (miR)-556-5p, and PTEN mRNA in NPC tissues and cells, RT-qPCR was employed. PTEN protein was quantified using western blot analysis. The impact of circ_0007439 on cellular activities was assessed using CCK-8, colony formation, Transwell, and flow cytometry, in that order. The interaction of miR-556-5p with circ_0007439 or PTEN mRNA was confirmed through a dual luciferase reporter gene assay and RIP assay.&lt;h4>Results&lt;/h4>circ_0007439 and PTEN levels were low in NPC tissues and cells, while miR-556-5p was highly expressed. NPC cells were i</pubmed_abstract><journal>Discover oncology</journal><pagination>807</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11655796</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Unveiling hsa_circ_0007439: a novel suppressor of nasopharyngeal carcinoma via miR-556-5p/PTEN Axis.</pubmed_title><pmcid>PMC11655796</pmcid><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Fu D</pubmed_authors><pubmed_authors>Feng W</pubmed_authors><pubmed_authors>Bai Y</pubmed_authors><pubmed_authors>Li M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Unveiling hsa_circ_0007439: a novel suppressor of nasopharyngeal carcinoma via miR-556-5p/PTEN Axis.</name><description>&lt;h4>Objective&lt;/h4>There has been no explanation for the exact mechanism of circRNAs in nasopharyngeal carcinoma (NPC). Circ_0007439 was investigated in this study to determine its role and mechanism in NPC.&lt;h4>Methods&lt;/h4>To identify circ_0007439, microRNA (miR)-556-5p, and PTEN mRNA in NPC tissues and cells, RT-qPCR was employed. PTEN protein was quantified using western blot analysis. The impact of circ_0007439 on cellular activities was assessed using CCK-8, colony formation, Transwell, and flow cytometry, in that order. The interaction of miR-556-5p with circ_0007439 or PTEN mRNA was confirmed through a dual luciferase reporter gene assay and RIP assay.&lt;h4>Results&lt;/h4>circ_0007439 and PTEN levels were low in NPC tissues and cells, while miR-556-5p was highly expressed. NPC cells were i</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-22T10:47:04.903Z</modification><creation>2025-04-05T23:41:41.648Z</creation></dates><accession>S-EPMC11655796</accession><cross_references><pubmed>39692840</pubmed><doi>10.1007/s12672-024-01656-z</doi></cross_references></HashMap>