In silico transcriptome screens identify epidermal growth factor receptor inhibitors as therapeutics for noise-induced hearing loss.
Sarath VijayakumarJoseph A DiGuiseppiParinaz Jila DabestaniWilliam G RyanRene Vielman QuevedoYuju LiJack DiersShu TuJonathan FleegelCassidy NguyenLauren M RhodaAli Sajid ImamiAbdul-Rizaq Ali HamoudSándor LovasRobert E McCullumsmithMarisa ZallocchiJian ZuoPublished in: Science advances (2024)
Noise-induced hearing loss (NIHL) is a common sensorineural hearing impairment that lacks U.S. Food and Drug Administration-approved drugs. To fill the gap in effective screening models, we used an in silico transcriptome-based drug screening approach, identifying 22 biological pathways and 64 potential small molecule treatments for NIHL. Two of these, afatinib and zorifertinib [epidermal growth factor receptor (EGFR) inhibitors], showed efficacy in zebrafish and mouse models. Further tests with EGFR knockout mice and EGF-morpholino zebrafish confirmed their protective role against NIHL. Molecular studies in mice highlighted EGFR's crucial involvement in NIHL and the protective effect of zorifertinib. When given orally, zorifertinib was found in the perilymph with favorable pharmacokinetics. In addition, zorifertinib combined with AZD5438 (a cyclin-dependent kinase 2 inhibitor) synergistically prevented NIHL in zebrafish. Our results underscore the potential for in silico transcriptome-based drug screening in diseases lacking efficient models and suggest EGFR inhibitors as potential treatments for NIHL, meriting clinical trials.
Keyphrases
- epidermal growth factor receptor
- hearing loss
- tyrosine kinase
- advanced non small cell lung cancer
- small molecule
- drug administration
- genome wide
- clinical trial
- rna seq
- molecular docking
- drug induced
- single cell
- gene expression
- human health
- high glucose
- diabetic rats
- mouse model
- air pollution
- dna methylation
- type diabetes
- adverse drug
- randomized controlled trial
- risk assessment
- growth factor
- emergency department
- skeletal muscle
- protein protein
- single molecule
- high throughput
- cell proliferation
- oxidative stress
- signaling pathway
- insulin resistance
- electronic health record
- stress induced