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寻常型银屑病患者血浆外泌体微小RNA水平的深度测序

Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients.

作者信息

Chen Xiu-Min, Yao Dan-Ni, Wang Mao-Jie, Wu Xiao-Dong, Deng Jing-Wen, Deng Hao, Huang Run-Yue, Lu Chuan-Jian

机构信息

State Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, China.

The Second Affiliated Hospital, Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou, China.

出版信息

Front Med (Lausanne). 2022 May 19;9:895564. doi: 10.3389/fmed.2022.895564. eCollection 2022.

Abstract

Psoriasis is a chronic skin disease affecting 1% to 3% of the world population. Psoriasis vulgaris (PV) is the most common form of psoriasis. PV patients suffer from inflamed, pruritic and painful lesions for years (even a lifetime). However, conventional drugs for PV are costly. Considering the need for long-term treatment of PV, it is urgent to discover novel biomarkers and therapeutic targets. Plasma exosomal miRNAs have been identified as the reliable biomarkers and therapy targets of human diseases. Here, we described the levels of serum exosomal miRNAs in PV patients and analyzed the functional features of differently expressed miRNAs and their potential target genes for the first time. We identified 1182 miRNAs including 336 novel miRNAs and 246 differently expressed miRNAs in serum exosomes of healthy people and PV patients. Furthermore, the functional analysis found differently expressed miRNA-regulated target genes enriched for specific GO terms including primary metabolic process, cellular metabolic process, metabolic process, organic substance metabolic process, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway containing cellular processes, human diseases, metabolic pathways, metabolism and organismal systems. In addition, we found that some predicted target genes of differentially expressed miRNAs, such as CREB1, RUNX2, EGFR, are both involved in inflammatory response and metabolism. In summary, our study identifies many candidate miRNAs involved in PV, which could provide potential biomarkers for diagnosis of PV and targets for clinical therapies against PV.

摘要

银屑病是一种慢性皮肤病,影响着全球1%至3%的人口。寻常型银屑病(PV)是银屑病最常见的形式。PV患者多年来(甚至终生)都遭受着炎症性、瘙痒性和疼痛性皮损的困扰。然而,用于PV的传统药物价格昂贵。考虑到PV需要长期治疗,迫切需要发现新的生物标志物和治疗靶点。血浆外泌体微小RNA(miRNA)已被确定为人类疾病的可靠生物标志物和治疗靶点。在此,我们首次描述了PV患者血清外泌体miRNA的水平,并分析了差异表达miRNA的功能特征及其潜在靶基因。我们在健康人和PV患者的血清外泌体中鉴定出1182种miRNA,包括336种新的miRNA和246种差异表达的miRNA。此外,功能分析发现差异表达的miRNA调控的靶基因富集于特定的基因本体(GO)术语,包括初级代谢过程、细胞代谢过程、代谢过程、有机物质代谢过程,以及京都基因与基因组百科全书(KEGG)通路,涵盖细胞过程、人类疾病、代谢通路、新陈代谢和机体系统。此外,我们发现一些差异表达miRNA的预测靶基因,如CREB1、RUNX2、表皮生长因子受体(EGFR),既参与炎症反应又参与新陈代谢。总之,我们的研究鉴定出许多与PV相关的候选miRNA,这可为PV的诊断提供潜在生物标志物,并为针对PV的临床治疗提供靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a381/9160332/6a2077f3a252/fmed-09-895564-g001.jpg

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