Suppr超能文献

中文译文:汉族人群圆锥角膜的转录组分析:差异基因表达及种族特异性模式的研究。

Transcriptomic analysis of keratoconus in Han Chinese patients: Insights into differential gene expression and ethnic-specific patterns.

机构信息

Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China; NHC Key Laboratory of Myopia and Related Eye Diseases, Key Laboratory of Myopia and Related Eye Diseases, Chinese Academy of Medical Sciences, Shanghai, China; Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China.

Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China; NHC Key Laboratory of Myopia and Related Eye Diseases, Key Laboratory of Myopia and Related Eye Diseases, Chinese Academy of Medical Sciences, Shanghai, China; Shanghai Key Laboratory of Visual Impairment and Restoration, Shanghai, China.

出版信息

Exp Eye Res. 2024 Nov;248:110118. doi: 10.1016/j.exer.2024.110118. Epub 2024 Oct 11.

Abstract

Keratoconus (KC) is a progressive corneal ectatic disorder with a high prevalence among Asians. This study aimed to explore the differential gene expression patterns in Han Chinese patients with KC, focusing on mRNAs and long noncoding RNAs (lncRNAs), to provide insights into the pathogenesis of the disease. Corneal tissues from KC patients and healthy controls were collected, and RNA sequencing was performed to profile mRNA and lncRNA expression. A total of 1973 differentially expressed mRNAs (DEGs) and 386 differentially expressed lncRNAs (DELs) were identified in KC-affected corneas. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses revealed significant enrichment in pathways related to ECM modulation, PI3K-Akt pathway and calcium signaling pathway. Furthermore, protein-protein interaction (PPI) network highlighted hub genes involved in ECM remodeling and inflammatory responses. Co-expression analysis of lncRNAs and mRNAs further prioritized 13 DELs linked to these hub genes. RT-qPCR validation confirmed the differential expression of select candidates. A meta-analysis integrating seven datasets from diverse ethnic backgrounds was performed and it suggested ethnic-specific differences in gene expression patterns. This study sheds new light on the molecular mechanisms underlying KC in the Han Chinese population, pinpointing potential therapeutic targets. It also emphasizes the critical role of ethnic-specific gene expression patterns in KC research, highlighting a need for tailored approaches in disease management and treatment.

摘要

圆锥角膜(KC)是一种进展性角膜扩张性疾病,在亚洲人中发病率较高。本研究旨在探索汉族 KC 患者差异表达基因的表达模式,重点关注 mRNAs 和长非编码 RNA(lncRNAs),以期深入了解该疾病的发病机制。收集 KC 患者和健康对照者的角膜组织,进行 RNA 测序以分析 mRNA 和 lncRNA 的表达。在 KC 病变角膜中,共鉴定到 1973 个差异表达的 mRNA(DEGs)和 386 个差异表达的 lncRNA(DELs)。GO 和 KEGG 富集分析显示,与 ECM 调节、PI3K-Akt 途径和钙信号途径相关的途径明显富集。此外,蛋白质-蛋白质相互作用(PPI)网络突出了参与 ECM 重塑和炎症反应的关键基因。lncRNA 和 mRNA 的共表达分析进一步确定了与这些关键基因相关的 13 个 DELs。RT-qPCR 验证证实了部分候选物的差异表达。对来自不同种族背景的七个数据集进行了荟萃分析,结果表明基因表达模式存在种族特异性差异。本研究揭示了汉族人群 KC 发病的分子机制,为潜在的治疗靶点提供了新的见解。它还强调了在 KC 研究中,种族特异性基因表达模式的重要性,突出了在疾病管理和治疗中需要采用个性化方法的必要性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验