Exploring the Molecular Mechanism of Hydroxychloroquine Against IgAN Through Network Pharmacology, MD Simulations and Experimental Assessment
Yuyuan Liu, Jinfang Hu, Jialing Wang, Yanzhe Wang, Gang Wu

TL;DR
This study explores how hydroxychloroquine treats IgA nephropathy by identifying key genes and proteins involved in inflammation and immune response.
Contribution
The study identifies PTGS2 as a key target of hydroxychloroquine in IgAN through network pharmacology and experimental validation.
Findings
Hydroxychloroquine targets 125 genes related to IgA nephropathy, including inflammation and immune pathways.
PTGS2 is overexpressed in IgAN patients and negatively correlates with kidney function.
Hydroxychloroquine reduces PTGS2 and profibrotic proteins in IgAN cell models.
Abstract
Hydroxychloroquine (HCQ) has recently been reported to be an effective treatment for IgA nephropathy (IgAN); however, the exact mechanism remains elusive. This study aimed to explore the molecular mechanisms of HCQ against IgAN. IgAN‐related genes and HCQ target sets were screened from online databases, and a section of them was identified as targets of HCQ against IgAN. In total, 1575 IgAN‐ related genes, 415 HCQ targets, and 125 targets of HCQ against IgAN were identified. The results of the enrichment analysis showed that the targets of HCQ against IgAN were related to inflammation and immune response related pathways. The PPI network and subnetworks identified prostaglandin‐endoperoxide synthase 2 (PTGS2) as the main seed gene. Molecular docking and molecular dynamic (MD) simulations revealed that HCQ could well bind to the PTGS2 protein. Furthermore, clinical data indicated that…
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Taxonomy
TopicsInflammatory mediators and NSAID effects · Pharmacogenetics and Drug Metabolism · Renal Diseases and Glomerulopathies
