Gene Signatures and Associated Transcription Factors of Allergic Rhinitis: KLF4 Expression Is Associated with Immune Response.

This study is aimed at investigating the potential molecular features of allergic rhinitis (AR) and identifying gene signatures and related transcription factors using transcriptome analysis and in silico datasets. Transcriptome profiles were obtained using three independent cohorts (GSE101720, GSE1...

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Publicado en:BioMed Research International pp. 1 - 13
Autores principales: Jeon, Youngsic, Kang, Tae Kyeom, Lee, Wook-Bin, Jung, Sang Hoon, Kim, Young-Joo
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell 5/10/2023
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 5/10/2023
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2023/1317998
        163659773
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        atl: Gene Signatures and Associated Transcription Factors of Allergic Rhinitis: KLF4 Expression Is Associated with Immune Response.
      aug:
        au:
          Jeon, Youngsic
          Kang, Tae Kyeom
          Lee, Wook-Bin
          Jung, Sang Hoon
          Kim, Young-Joo
        affil: Natural Product Research Center, Korea Institute of Science and Technology, Gangneung, Republic of Korea
      sug:
        subj:
          Rhinitis, Allergic, Perennial Familial and Genetic
          Rhinitis, Allergic, Seasonal Familial and Genetic
          Rhinitis, Allergic, Perennial Pathology
          Rhinitis, Allergic, Seasonal Pathology
          Transcription Factors Analysis
          Gene Expression Profiling
          Pathology, Molecular
          Human
          Comparative Studies
          Gene Expression
          Funding Source
          Epithelial Cells Immunology
          Nasal Mucosa Immunology
          Transcription Factors Immunology
      ab: This study is aimed at investigating the potential molecular features of allergic rhinitis (AR) and identifying gene signatures and related transcription factors using transcriptome analysis and in silico datasets. Transcriptome profiles were obtained using three independent cohorts (GSE101720, GSE19190, and GSE46171) comprising healthy controls (HC) and patients with AR. The pooled dataset (n = 82) was used to identify the critical signatures of AR compared with HC. Subsequently, key transcription factors were identified by a combined analysis using transcriptome and in silico datasets. Gene ontology: bioprocess (GO: BP) analysis using differentially expressed genes (DEGs) revealed that immune response-related genes were significantly enriched in AR compared with HC. Among them, IL1RL1, CD274, and CD44 were significantly higher in AR patients. We also identified key transcription factors between HC and AR using the in silico dataset and found that AR samples frequently express KLF transcription factor 4 (KLF4), which regulates immune response-related genes including IL1RL1, CD274, and CD44 in human nasal epithelial cells. Our integrative analysis of transcriptomic regulation provides new insights into AR, which may help in developing precision management for patients with AR.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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