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Differential microRNA profiles in elderly males with seborrheic dermatitis

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dc.contributor.authorHyejun Kim-
dc.contributor.authorJae Won Yun-
dc.contributor.authorGayun Baek-
dc.contributor.authorSungchul Kim-
dc.contributor.authorMihn-Sook Jue-
dc.date.accessioned2023-01-26T02:25:48Z-
dc.date.available2023-01-26T02:25:48Z-
dc.date.created2022-12-16-
dc.date.issued2022-12-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/12502-
dc.description.abstractSeborrheic dermatitis (SD) is one of the most common skin diseases characterized by inflammatory symptoms and cell proliferation, which has increased incidence in patients older than 50 years. Although the roles of microRNAs (miRNAs) have been investigated in several diseases, miRNA profiles of patients with SD remain unknown. This study aimed to identify differentially expressed miRNAs (DEMs) in lesions of elderly male patients with SD. We used a microarray-based approach to identify DEMs in lesions compared to those in non-lesions of patients with SD. Furthermore, Gene Ontology and pathway enrichment analysis were performed using bioinformatics tools to elucidate the functional significance of the target mRNAs of DEMs in lesions of patients with SD. Expression levels of two miRNAs-hsa-miR-6831-5p and hsa-miR-7107-5p-were downregulated, whereas those of six miRNAs-hsa-miR-20a-5p, hsa-miR-191-5p, hsa-miR-127-3p, hsa-miR-106b-5p, hsa-miR-342-3p, and hsa-miR-6824-5p-were upregulated. Functions of the SD-related miRNAs were predicted to be significantly associated with typical dermatological pathogenesis, such as cell proliferation, cell cycle, apoptosis, and immune regulation. In summary, SD alters the miRNA profile, and target mRNAs of the DEMs are related to immune responses and cell proliferation, which are the two main processes in SD pathogenesis. © 2022. The Author(s).-
dc.language영어-
dc.publisherNLM (Medline)-
dc.titleDifferential microRNA profiles in elderly males with seborrheic dermatitis-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000992275200031-
dc.identifier.scopusid2-s2.0-85143559727-
dc.identifier.rimsid79450-
dc.contributor.affiliatedAuthorHyejun Kim-
dc.contributor.affiliatedAuthorSungchul Kim-
dc.identifier.doi10.1038/s41598-022-24383-3-
dc.identifier.bibliographicCitationScientific reports, v.12, no.1-
dc.relation.isPartOfScientific reports-
dc.citation.titleScientific reports-
dc.citation.volume12-
dc.citation.number1-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusGENE LISTS-
dc.subject.keywordPlusMALASSEZIA-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusETIOLOGY-
dc.subject.keywordPlusREACTOME-
Appears in Collections:
Center for RNA Research(RNA 연구단) > 1. Journal Papers (저널논문)
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