Science AdvancesNeurosciencePeer-reviewed journal article
In Silico Transcriptome-based Screens Identify Epidermal Growth Factor Receptor Inhibitors as Therapeutics for Noise-induced Hearing Loss
Sarath VijayakumariD, Joseph DiGuiseppiiD, Parinaz J. DabestaniiD, William G. RyaniD, René Vielman QuevedoiD, Yuju Li, Jack Diers, Shu Tu, Jonathan P. FleegeliD, Cassidy Nguyen, Lauren M. Rhoda, Ali Sajid ImamiiD, Abdul-Rizaq Ali HamoudiD, Sándor LovasiD, Robert Erne McCullumsmithiD, Marisa ZallocchiiD, Jian ZuoiD
Abstract
Noise-Induced Hearing Loss (NIHL) represents a widespread disease for which no therapeutics have been approved by the Food and Drug Administration (FDA). Addressing the conspicuous void of efficacious in vitro or animal models for high throughput pharmacological screening, we utilized an in silico transcriptome-oriented drug screening strategy, unveiling 22 biological pathways and 64 promising small molecule candidates for NIHL protection. Afatinib and zorifertinib, both inhibitors of the Epidermal Growth Factor Receptor (EGFR), were validated for their protective efficacy against NIHL in experimental zebrafish and murine models. This protective effect was further confirmed with EGFR conditional knockout mice and EGF knockdown zebrafish, both demonstrating protection against NIHL. Molecular analysis using Western blot and kinome signaling arrays on adult mouse cochlear lysates unveiled the intricate involvement of several signaling pathways, with particular emphasis on EGFR and its downstream pathways being modulated by noise exposure and Zorifertinib treatment. Administered orally, Zorifertinib was successfully detected in the perilymph fluid of the inner ear in mice with favorable pharmacokinetic attributes. Zorifertinib, in conjunction with AZD5438 - a potent inhibitor of cyclin dependent kinase 2 - produced synergistic protection against NIHL in the zebrafish model. Collectively, our findings underscore the potential application of in silico transcriptome-based drug screening for diseases bereft of efficient screening models and posit EGFR inhibitors as promising therapeutic agents warranting clinical exploration for combatting NIHL. HighlightsO_LIIn silico transcriptome-based drug screens identify pathways and drugs against NIHL. C_LIO_LIEGFR signaling is activated by noise but reduced by zorifertinib in mouse cochleae. C_LIO_LIAfatinib, zorifertinib and EGFR knockout protect against NIHL in mice and zebrafish. C_LIO_LIOrally delivered zorifertinib has inner ear PK and synergizes with a CDK2 inhibitor. C_LI
- organism: mouse
- organism: zebrafish
- assay: bulk RNA-seq
- research focus: drug response / drug discovery
- approach: statistical model
- Citations
- 12
- FWCI
- 3.34
- Field percentile
- top 7%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- In silico transcriptomics identifies FDA-approved drugs and biological pathways for protection against cisplatin-induced hearing loss
Pezhman Salehi, Marisa Zallocchi, … Jian Zuo·bioRxiv·Jan 26, 2022
- ERK1/2 Inhibition Alleviates Noise-Induced Hearing Loss While Tempering Down the Immune Response
Richard D. Lutze, Matthew A. Ingersoll, … Tal Teitz·International Journal of Molecular SciencesPeer-reviewed·Jun 7, 2024
- Resolving early cochlear inflammation prevents lasting damage from noise exposure
Lauren Barbush, Klim Fedorchuk, … Marisa Zallocchi·bioRxiv·Jul 17, 2026
- Oseltamivir (Tamiflu), a Commonly Prescribed Antiviral Drug, Mitigates Hearing Loss in Mice
Emma J. Sailor‐Longsworth, Richard D. Lutze, … Tal Teitz·Clinical and Translational MedicinePeer-reviewed·Aug 1, 2024
- Heat-shock pathway activation by TRC051384 protects spiral ganglion neurons from noise-induced hearing loss
Jintao Yu, Miguel A. Ramirez, … Jeffrey N. Savas·JCI InsightPeer-reviewed·Aug 25, 2026
- FDA-Approved MEK1/2 Inhibitor, Trametinib, Protects Mice from Cisplatin and Noise-Induced Hearing Loss
Richard D. Lutze, Matthew A. Ingersoll, … Tal Teitz·PharmaceuticalsPeer-reviewed·Jun 5, 2024