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基于批量 RNA 条码和测序的嗜酸粒细胞性和非嗜酸粒细胞性慢性鼻-鼻窦炎伴鼻息肉的独特基因集富集图谱。

Distinct Gene Set Enrichment Profiles in Eosinophilic and Non-Eosinophilic Chronic Rhinosinusitis with Nasal Polyps by Bulk RNA Barcoding and Sequencing.

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Hiroshima 734-8551, Japan.

出版信息

Int J Mol Sci. 2022 May 18;23(10):5653. doi: 10.3390/ijms23105653.

Abstract

Chronic rhinosinusitis with nasal polyps (CRSwNP) is a chronic inflammatory disease with a high symptom burden, including nasal congestion and smell disorders. This study performed a detailed transcriptomic analysis in CRSwNP classified as eosinophilic CRS (ECRS), nonECRS according to the Japanese Epidemiological Survey of Refractory Eosinophilic Chronic Rhinosinusitis (JESREC) criteria, and a group of ECRS with comorbid aspirin intolerant asthma (Asp). Gene expression profiles of nasal polyps and the uncinate process in CRSwNP patients and normal subjects (controls) were generated by bulk RNA barcoding and sequencing (BRB-seq). A differentially expressed genes (DEGs) analysis was performed using DESeq2 software in iDEP to clarify any relationship between gene expression and disease backgrounds. A total of 3004 genes were identified by DEGs analysis to be associated with ECRS vs control, nonECRS vs control, and Asp vs control. A pathway analysis showed distinct profiles between the groups. A Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis using the Database for Annotation, Visualization, and Integrated Discovery (DAVID) showed distinct phenotype-specific pathways of expressed genes. In the specific pathway of "cytokine-cytokine receptor interaction", the differentially expressed genes were widely distributed. This study indicates that transcriptome analysis using BRB-seq may be a valuable tool to explore the pathogenesis of type 2 inflammation in CRSwNP.

摘要

伴有鼻息肉的慢性鼻-鼻窦炎(CRSwNP)是一种具有高症状负担的慢性炎症性疾病,包括鼻塞和嗅觉障碍。本研究根据日本难治性嗜酸性慢性鼻-鼻窦炎(JESREC)标准对嗜酸性 CRS(ECRS)、非 ECRS 以及伴有阿司匹林不耐受哮喘(Asp)的 ECRS 进行了详细的转录组分析。通过批量 RNA 条形码和测序(BRB-seq)对 CRSwNP 患者和正常受试者(对照)的鼻息肉和钩突的基因表达谱进行了分析。在 iDEP 中使用 DESeq2 软件进行差异表达基因(DEGs)分析,以明确基因表达与疾病背景之间的关系。通过 DEGs 分析,共鉴定出 3004 个与 ECRS 与对照、非 ECRS 与对照和 Asp 与对照相关的基因。通路分析显示各组之间存在明显的差异。使用数据库 for Annotation, Visualization, and Integrated Discovery(DAVID)对京都基因与基因组百科全书(KEGG)通路进行分析,显示出表达基因的特定表型特异性途径。在“细胞因子-细胞因子受体相互作用”的特定途径中,差异表达基因广泛分布。本研究表明,使用 BRB-seq 进行转录组分析可能是探索 CRSwNP 2 型炎症发病机制的一种有价值的工具。

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