# Identifying Therapeutic Targets for Bronchial Asthma: Systematic Druggable Genome‐Wide Mendelian Randomization

**Authors:** Haijiao Wang, Peng Zhang, Hongpeng Yu, Li Shi, Tan Wang

PMC · DOI: 10.1002/hsr2.71674 · Health Science Reports · 2026-01-21

## TL;DR

This study identifies six potential drug targets for bronchial asthma using genetic analysis, offering new insights for more effective treatments.

## Contribution

A systematic druggable genome-wide Mendelian randomization analysis to discover novel asthma therapeutic targets.

## Key findings

- Six druggable genes were identified as significantly associated with asthma.
- Most of the identified genes showed no side effects in phenome-wide analysis.

## Abstract

The treatment and prevention of bronchial asthma continue to present significant challenges. Mendelian randomization (MR) has been extensively employed to identify novel therapeutic targets. Consequently, we conducted a systematic MR analysis across the druggable genome to identify potential therapeutic targets for asthma.

Exploring new potential therapeutic targets for the treatment of asthma.

We obtained data on druggable genes and screened genes within lung expression quantitative trait loci (eQTL) and blood eQTL. Then, MR analysis and colocalization analysis were performed to identify genes highly associated with asthma. In addition, phenome‐wide analysis, enrichment analysis and protein–protein interaction network construction (PPI) have been carried out, providing valuable guidance for the development of more effective therapeutic targets.

Druggable genes were sourced from the Drug‐Gene Interaction Database (DGIdb) and supplemented by a compilation of druggable genes outlined in a review by Finan et al. The eQTL data sets are derived from eQTLGene and GTEx v8. We obtained asthma GWAS data sets from two large‐scale genotypic data sets, FinnGen, and UK Biobank. Finally, we identified six druggable genes significantly associated with asthma. Five druggable genes in whole blood (IRF1, OXER1, PSMA4, UNC13D and HLA‐DRB1) and one in lung tissue (CD226). These positive gene interactions were shown to be associated with asthma pathways by enrichment analysis. In the end, phenome‐wide analysis showed that most had no side effects.

This study identified six potential drug targets for the treatment of asthma. This discovery provides promising insights for more effective treatments for asthma, with the potential to reduce drug development costs.

## Linked entities

- **Genes:** IRF1 (interferon regulatory factor 1) [NCBI Gene 3659], OXER1 (oxoeicosanoid receptor 1) [NCBI Gene 165140], PSMA4 (proteasome 20S subunit alpha 4) [NCBI Gene 5685], UNC13D (unc-13 homolog D) [NCBI Gene 201294], HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123], CD226 (CD226 molecule) [NCBI Gene 10666]

## Full-text entities

- **Genes:** CD226 (CD226 molecule) [NCBI Gene 10666] {aka DNAM-1, DNAM1, PTA1, TLiSA1}, IRF1 (interferon regulatory factor 1) [NCBI Gene 3659] {aka IMD117, IRF-1, MAR}, PSMA4 (proteasome 20S subunit alpha 4) [NCBI Gene 5685] {aka HC9, HsT17706, PSC9}, HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, OXER1 (oxoeicosanoid receptor 1) [NCBI Gene 165140] {aka GPCR, GPR170, TG1019}, UNC13D (unc-13 homolog D) [NCBI Gene 201294] {aka HLH3, HPLH3, Munc13-4}
- **Diseases:** Bronchial Asthma (MESH:D001249)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12820719/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12820719/full.md

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Source: https://tomesphere.com/paper/PMC12820719