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银屑病精准医学候选基因的生物信息学分析与转化验证

Bioinformatic Analysis and Translational Validation of Psoriasis Candidate Genes for Precision Medicine.

作者信息

Li An-Hai, Li Wen-Wen, Yu Xiao-Qian, Zhang Dai-Ming, Liu Yi-Ran, Li Ding

机构信息

Department of Dermatology, Qingdao Huangdao District Central Hospital, Qingdao, People's Republic of China.

Department of Hematology, Qingdao Women and Children's Hospital, Qingdao, People's Republic of China.

出版信息

Clin Cosmet Investig Dermatol. 2022 Jul 28;15:1447-1458. doi: 10.2147/CCID.S378143. eCollection 2022.

DOI:10.2147/CCID.S378143
PMID:35924255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9343179/
Abstract

BACKGROUND

Psoriasis is a recurrent, chronic, inflammation- and immune-mediated skin disease with multiple causative factors. However, the genetic markers associated with recurrence have not yet been fully elucidated. Accordingly, in this study, we aimed to identify markers associated with the recurrence of psoriasis.

METHODS

We analyzed differentially expressed genes to determine which targets were associated with the recurrence of psoriasis and used these data to construct a protein-protein interaction network using Cytoscape software. The results were then validated by analysis of core targets using Gene Expression Omnibus (GEO) datasets and clinical samples. Functional enrichment analysis was used to explore the potential mechanisms mediating the recurrence of psoriasis.

RESULTS

We screened out six core targets that played important roles in recurrence of psoriasis, and validation of GEO datasets and clinical samples showed that the expression levels of five core targets were higher in patients with psoriasis than in healthy individuals. Functional enrichment analysis revealed that the cell cycle and oocyte meiosis signaling pathways were involved in the recurrence of psoriasis.

CONCLUSION

Our findings provided insights into the mechanisms mediating the onset and recurrence of psoriasis.

摘要

背景

银屑病是一种由多种致病因素引起的复发性、慢性、炎症和免疫介导的皮肤病。然而,与复发相关的遗传标记尚未完全阐明。因此,在本研究中,我们旨在确定与银屑病复发相关的标记。

方法

我们分析差异表达基因以确定哪些靶点与银屑病复发相关,并使用这些数据通过Cytoscape软件构建蛋白质-蛋白质相互作用网络。然后通过使用基因表达综合数据库(GEO)数据集和临床样本对核心靶点进行分析来验证结果。功能富集分析用于探索介导银屑病复发的潜在机制。

结果

我们筛选出六个在银屑病复发中起重要作用的核心靶点,GEO数据集和临床样本的验证表明,五个核心靶点在银屑病患者中的表达水平高于健康个体。功能富集分析显示细胞周期和卵母细胞减数分裂信号通路参与了银屑病的复发。

结论

我们的研究结果为介导银屑病发病和复发的机制提供了见解。

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Secukinumab Loss of Efficacy Is Perfectly Counteracted by the Introduction of Combination Therapy (Rescue Therapy): Data from a Multicenter Real-Life Study in a Cohort of Italian Psoriatic Patients That Avoided Secukinumab Switching.通过引入联合治疗(挽救治疗)可完美抵消司库奇尤单抗的疗效丧失:来自一项针对意大利银屑病患者队列的多中心真实世界研究的数据,该研究避免了司库奇尤单抗的换药。
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Clinical trait-connected network analysis reveals transcriptional markers of active psoriasis treatment with Liangxue-Jiedu decoction.临床特征关联网络分析揭示了凉血解毒汤治疗活动性银屑病的转录标志物。
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Galectin-8 Is Upregulated in Keratinocytes by IL-17A and Promotes Proliferation by Regulating Mitosis in Psoriasis.半乳糖凝集素-8 可被白细胞介素-17A 上调,并通过调节有丝分裂促进银屑病角质形成细胞增殖。
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Intermittent use of biologic agents for the treatment of psoriasis in adults.间歇性使用生物制剂治疗成人银屑病。
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