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
- genome wide
- drug administration
- rna seq
- clinical trial
- drug induced
- molecular docking
- single cell
- gene expression
- human health
- high glucose
- diabetic rats
- air pollution
- mouse model
- small cell lung cancer
- type diabetes
- risk assessment
- high throughput
- growth factor
- climate change
- metabolic syndrome
- emergency department
- cell death
- cell proliferation
- insulin resistance
- study protocol
- signaling pathway
- case control