Proteins in skin and blood in patients with psoriasis: a systematic review of proteomic studies

被引:6
作者
Hansen, Bjorn Kromann [1 ,2 ]
Olsson, Anna [1 ,2 ]
Zhang, Ying Marlene [1 ,2 ]
Lovendorf, Marianne Bengtson [1 ,2 ,3 ]
Skov, Lone [1 ,2 ,4 ]
Dyring-Andersen, Beatrice [1 ,2 ,3 ,5 ]
机构
[1] Copenhagen Univ Hosp Herlev & Gentofte, Dept Dermatol & Allergy, Hellerup, Denmark
[2] Copenhagen Univ Hosp, Dept Dermatol & Allergy, Gentofte, Denmark
[3] Univ Copenhagen, Fac Hlth & Med Sci, Leo Foundat Skin Immunol Res Ctr, Copenhagen, Denmark
[4] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[5] Univ Copenhagen, Novo Nord Fdn NNF Ctr Prot Res, Fac Hlth & Med Sci, Copenhagen, Denmark
关键词
proteomics; psoriasis; systematic review; skin; blood; EXPRESSION; PATHWAY; DIFFERENTIATION; INTERLEUKIN-16; IDENTIFICATION; INFLAMMATION; ACTIVATION; CHEMOKINES; SIMILARITY; BIOMARKERS;
D O I
10.1159/000533981
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Proteins play a central role in psoriasis as they are involved in the structural phenotypic changes and inflammation that characterize the disease. This systematic review aims to assess which proteins have been consistently reported as upregulated or downregulated in skin and blood from patients with psoriasis. Methods: We included proteomic studies reporting differentially expressed proteins (DEPs) in at least one of four predefined comparisons using a standardized procedure to extract and align data. Network analysis of functional protein associations was made with StringApp in Cytoscape. A protocol for this review was registered in the PROSPERO database (ref:CRD42022363226). Results: We identified and assessed 772 studies published between 1996-12-02 and 2023-04-28, among which 30 studies met the inclusion and data availability criteria for analysis that together reported a sum of 5314 DEPs. The majority of consistently reported upregulated and downregulated proteins were found in lesional versus non-lesional skin (n=313) followed by lesional versus healthy skin (n=185), blood from patients with psoriasis versus blood from healthy individuals (n=140) and non-lesional versus healthy skin (n=1). Network analysis of upregulated proteins revealed different functional clusters with interleukin(IL)-6, IL-8, IL-17A, C-C motif chemokine (CCL) 20, signal transducer and activator of transcription (STAT) 3 and interferon(IFN)-gamma along with less well studied proteins playing central roles. Some of the reported changes are associated with anti-inflammatory effects. Additionally, the proteomic dysregulation also included antimicrobial peptides, alarmins, angiogenic factors and proteins related to protein synthesis. Conclusion: Our findings generally support current understandings of the pathological mechanisms in psoriasis. Importantly, some consistent findings have not been discussed before and deserve attention in future research.
引用
收藏
页码:317 / 328
页数:12
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