Identification of galangin as a therapeutic candidate for primary biliary cholangitis via systematic druggable genome-wide Mendelian randomization analysis and experimental validation

By integrating systematic druggable genome-wide MR analysis with experimental validation, this study identified 15 druggable genes associated with PBC. More importantly, it identified GAL as a therapeutic candidate for PBC, with its effects potentially mediated by the ADORA2A target. These findings provide novel therapeutic targets and drugs for PBC. Future research will focus on validating the functions of these druggable genes and elucidating the mechanistic pathway of the galangin-ADORA2A interaction, laying a more solid and comprehensive theoretical and practical foundation for PBC treatment.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2025-10-09
DOI
https://doi.org/10.3389/fphar.2025.1674693
Primary Topic
Liver Diseases and Immunity
Type
article
Field-Weighted Citation Impact
0.00

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article

Identification of galangin as a therapeutic candidate for primary biliary cholangitis via systematic druggable genome-wide Mendelian randomization analysis and experimental validation

Chuang Zhang, Hanyan Wang, Weirui Ren, Suxian Zhao et al.
Frontiers in Pharmacology
Liver Diseases and Immunity
article

Identification of galangin as a therapeutic candidate for primary biliary cholangitis via systematic druggable genome-wide Mendelian randomization analysis and experimental validation

Chuang Zhang, Hanyan Wang, Weirui Ren, Suxian Zhao, Zhijun Zhang, Junmin Wang, Huai‐Dong Song, X.P. Zhu
article en

Abstract

By integrating systematic druggable genome-wide MR analysis with experimental validation, this study identified 15 druggable genes associated with PBC. More importantly, it identified GAL as a therapeutic candidate for PBC, with its effects potentially mediated by the ADORA2A target. These findings provide novel therapeutic targets and drugs for PBC. Future research will focus on validating the functions of these druggable genes and elucidating the mechanistic pathway of the galangin-ADORA2A interaction, laying a more solid and comprehensive theoretical and practical foundation for PBC treatment.

Frontiers in PharmacologyVol. 16
Hebei Medical University (CN), Shijiazhuang University (CN), Third Hospital of Hebei Medical University (CN)
Hebei Medical University
Openalex Percentile: Top 62%
Liver Diseases and Immunity
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