Integrative multi-omics analysis reveals gut-skin axis mechanisms and novel therapeutic target <i>GALE</i> in atopic dermatitis

Genetic-level evidence of gut microbiota causality in atopic dermatitis: this study established a causal relationship between specific gut microbiota and the risk of atopic dermatitis at the genetic level, providing strong genetic evidence for the "gut-skin axis" theory. GALE is identified as a novel therapeutic target with redefined methotrexate mechanism: molecular docking study unexpectedly found that GALE binding affinity of MTX was significantly higher than that of its classical target TYMS, suggesting that GALE may be an important but previously unrecognized target of MTX in the treatment of AD. Multi-omics integration framework reveals increased keratinocyte heterogeneity: integrating single-cell RNA sequencing and computational pharmacology provided a cellular and molecular basis for understanding the characteristics of chronicity and recurrence of the disease.

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Publication Details

Journal
mSystems
Published
2025-12-05
DOI
https://doi.org/10.1128/msystems.01403-25
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Integrative multi-omics analysis reveals gut-skin axis mechanisms and novel therapeutic target GALE in atopic dermatitis

Jing Guo, Qianying Yu, Yaobin Pang, Jinlu Tong et al.
mSystems
Dermatology and Skin Diseases
article

Integrative multi-omics analysis reveals gut-skin axis mechanisms and novel therapeutic target GALE in atopic dermatitis

Jing Guo, Qianying Yu, Yaobin Pang, Jinlu Tong, Cui Guo, Hui Zhang, Aimin Liu, Fang Cao, K.T. Tang
article en

Abstract

Genetic-level evidence of gut microbiota causality in atopic dermatitis: this study established a causal relationship between specific gut microbiota and the risk of atopic dermatitis at the genetic level, providing strong genetic evidence for the "gut-skin axis" theory. GALE is identified as a novel therapeutic target with redefined methotrexate mechanism: molecular docking study unexpectedly found that GALE binding affinity of MTX was significantly higher than that of its classical target TYMS, suggesting that GALE may be an important but previously unrecognized target of MTX in the treatment of AD. Multi-omics integration framework reveals increased keratinocyte heterogeneity: integrating single-cell RNA sequencing and computational pharmacology provided a cellular and molecular basis for understanding the characteristics of chronicity and recurrence of the disease.

mSystemsVol. 11(1)
Shanghai Jiao Tong University (CN), Southwest Hospital (CN), Chengdu University of Traditional Chinese Medicine (CN)
Openalex Percentile: Top 38%
Dermatology and Skin Diseases
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