<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Smith-Davidson P</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>CCR NIH HHS</funding><funding>Intramural NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>NIDCD NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Institute on Deafness and Other Communication Disorders</funding><funding>NCI NIH HHS</funding><funding>Center for Cancer Research</funding><pagination>S1-S8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11903372</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>135 Suppl 1</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Allergic fungal rhinosinusitis (AFRS) is an eosinophilic subtype of chronic rhinosinusitis with nasal polyposis (CRSwNP). This study aimed to investigate the transcriptome of AFRS nasal polyp epithelium.&lt;h4>Methods&lt;/h4>Sinonasal epithelial cells were harvested from healthy nasal mucosa and polyp tissue collected from participants undergoing elective sinonasal surgery. Primary epithelial cells were subsequently grown in air/liquid interface and subjected to RNA-seq analysis, RT-qPCR, immunoblotting, and immunostaining.&lt;h4>Results&lt;/h4>A total of 19 genes were differentially expressed between healthy and AFRS sample epithelium. The second top candidate gene, ranked by adjusted p-value, was prostaglandin E receptor 2 (PTGER2). The upregulation of PTGER2 was confirmed by RT-qPCR and immunoblot. The presence of the EP2 receptor, encoded by the PTGER2 gene, was confirmed by immunocytochemistry.&lt;h4>Conclusion&lt;/h4>PTGER2 is a potential novel therapeutic target for AFRS. EP2 dysregulation is associated with aspirin-exacerbated respiratory disease, potentially giving insight into common mechanisms of disease in severe CRSwNP.&lt;h4>Level of evidence&lt;/h4>NA Laryngoscope, 135:S1-S8, 2025.</pubmed_abstract><journal>The Laryngoscope</journal><pubmed_title>Prostaglandin E Receptor 2 (EP2) Dysregulation in Allergic Fungal Rhinosinusitis Nasal Polyp Epithelium.</pubmed_title><pmcid>PMC11903372</pmcid><funding_grant_id>R03TR004022</funding_grant_id><funding_grant_id>F32 DC000097</funding_grant_id><funding_grant_id>UL1 TR002378</funding_grant_id><funding_grant_id>P30 CA138292</funding_grant_id><funding_grant_id>UL1TR002378</funding_grant_id><funding_grant_id>R01‐HL158979</funding_grant_id><funding_grant_id>DC000097</funding_grant_id><funding_grant_id>P30CA138292</funding_grant_id><funding_grant_id>R01-HL158979</funding_grant_id><funding_grant_id>R03 TR004022</funding_grant_id><funding_grant_id>R01 HL158979</funding_grant_id><funding_grant_id>ZIA DC000098</funding_grant_id><pubmed_authors>Kabongo MM</pubmed_authors><pubmed_authors>DelGaudio JM</pubmed_authors><pubmed_authors>Koval M</pubmed_authors><pubmed_authors>Magliocca KR</pubmed_authors><pubmed_authors>Altartoor K</pubmed_authors><pubmed_authors>Solares CA</pubmed_authors><pubmed_authors>Claussen H</pubmed_authors><pubmed_authors>Levy JM</pubmed_authors><pubmed_authors>Johnston HR</pubmed_authors><pubmed_authors>Wise SK</pubmed_authors><pubmed_authors>Barrow EM</pubmed_authors><pubmed_authors>Smith-Davidson P</pubmed_authors><pubmed_authors>Arthur RA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prostaglandin E Receptor 2 (EP2) Dysregulation in Allergic Fungal Rhinosinusitis Nasal Polyp Epithelium.</name><description>&lt;h4>Objectives&lt;/h4>Allergic fungal rhinosinusitis (AFRS) is an eosinophilic subtype of chronic rhinosinusitis with nasal polyposis (CRSwNP). This study aimed to investigate the transcriptome of AFRS nasal polyp epithelium.&lt;h4>Methods&lt;/h4>Sinonasal epithelial cells were harvested from healthy nasal mucosa and polyp tissue collected from participants undergoing elective sinonasal surgery. Primary epithelial cells were subsequently grown in air/liquid interface and subjected to RNA-seq analysis, RT-qPCR, immunoblotting, and immunostaining.&lt;h4>Results&lt;/h4>A total of 19 genes were differentially expressed between healthy and AFRS sample epithelium. The second top candidate gene, ranked by adjusted p-value, was prostaglandin E receptor 2 (PTGER2). The upregulation of PTGER2 was confirmed by RT-qPCR and immunoblot. The presence of the EP2 receptor, encoded by the PTGER2 gene, was confirmed by immunocytochemistry.&lt;h4>Conclusion&lt;/h4>PTGER2 is a potential novel therapeutic target for AFRS. EP2 dysregulation is associated with aspirin-exacerbated respiratory disease, potentially giving insight into common mechanisms of disease in severe CRSwNP.&lt;h4>Level of evidence&lt;/h4>NA Laryngoscope, 135:S1-S8, 2025.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-06-02T21:05:13.028Z</modification><creation>2025-04-03T23:56:44.631Z</creation></dates><accession>S-EPMC11903372</accession><cross_references><pubmed>39487665</pubmed><doi>10.1002/lary.31868</doi></cross_references></HashMap>