Evidence map›Paper›PMID 42222449›Full record

ArticlePostepy dermatologii i alergologii2026

Shared molecular mechanisms of vascular endothelial cells in psoriasis and diabetes comorbidity.

Jiaxin Xu, Xin Zhang, Tianyuan Zhang, Gang Wang, Qingyang Li

Abstract read
In one paragraph

Article in Postepy dermatologii i alergologii, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jiaxin XuDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Xin ZhangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Tianyuan ZhangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Gang WangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Qingyang LiDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Dysfunction of vascular endothelial cells (VECs) is a common feature of both psoriasis and diabetes. Comorbidity of these two conditions increases the risk of diabetic foot ulcer (DFU), yet the shared mechanisms remain unclear. Aim: This study aimed to systematically elucidate the shared pathological mechanisms of the two diseases from the perspective of VECs and explore their association with the pathogenesis of DFU. Material and methods: We integrated and analysed single-cell transcriptomic data from skin samples of healthy controls, psoriasis patients, diabetes patients, and DFU patients. VECs were clustered and annotated, followed by application of differential expression analysis, weighted gene co-expression network analysis, and protein-protein interaction network analysis. Results: VECs could be classified into five distinct subclusters. We identified 561 co-upregulated genes in VECs from both psoriasis and diabetes, and 12 core shared genes (e.g., CEBPB, ABL2) were further pinpointed, which were highly expressed in clusters A and P and showed upregulation under Conclusions: This study provides an explanation for the comorbidity mechanism of psoriasis and diabetes as well as the risk of vascular complications, laying a foundation for developing cross-disease therapeutic strategies targeting VECs.

Indexed as

diabetesdiabetic foot ulcerpsoriasisvascular endothelial cell

Identifiers

PMID42222449
PMCPMC13217162

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