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计算机转录组筛选鉴定表皮生长因子受体抑制剂可作为治疗噪声性听力损失的药物。

In silico transcriptome screens identify epidermal growth factor receptor inhibitors as therapeutics for noise-induced hearing loss.

机构信息

Department of Biomedical Sciences, School of Medicine, Creighton University, Omaha, NE 68178, USA.

Department of Neurosciences, University of Toledo, Toledo, OH 43614, USA.

出版信息

Sci Adv. 2024 Jun 21;10(25):eadk2299. doi: 10.1126/sciadv.adk2299. Epub 2024 Jun 19.


DOI:10.1126/sciadv.adk2299
PMID:38896614
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11186505/
Abstract

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.

摘要

噪声性听力损失(NIHL)是一种常见的感觉神经性听力障碍,缺乏美国食品和药物管理局批准的药物。为了填补有效的筛选模型的空白,我们使用基于转录组的计算机药物筛选方法,确定了 22 种生物途径和 64 种潜在的用于 NIHL 的小分子治疗方法。其中两种,阿法替尼和佐利替尼[表皮生长因子受体(EGFR)抑制剂],在斑马鱼和小鼠模型中显示出疗效。对 EGFR 敲除小鼠和 EGF-Morpholino 斑马鱼的进一步测试证实了它们对 NIHL 的保护作用。在小鼠中的分子研究强调了 EGFR 在 NIHL 中的关键作用以及佐利替尼的保护作用。当口服给予时,佐利替尼在耳淋巴液中有良好的药代动力学。此外,佐利替尼与 AZD5438(细胞周期蛋白依赖性激酶 2 抑制剂)联合使用在斑马鱼中协同预防 NIHL。我们的结果强调了在缺乏有效模型的疾病中基于转录组的计算机药物筛选的潜力,并提出 EGFR 抑制剂作为 NIHL 的潜在治疗方法,值得进行临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/a42f3922d111/sciadv.adk2299-f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/b21b1f2924c2/sciadv.adk2299-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/6e5a669d7b51/sciadv.adk2299-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/695f7ae5009c/sciadv.adk2299-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/8c64b79ca900/sciadv.adk2299-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/9170fd2cd9d5/sciadv.adk2299-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/d2d995cef93f/sciadv.adk2299-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/f5217fe70658/sciadv.adk2299-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/53de11d081e2/sciadv.adk2299-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/e9e9555ebb05/sciadv.adk2299-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/a42f3922d111/sciadv.adk2299-f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/b21b1f2924c2/sciadv.adk2299-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/6e5a669d7b51/sciadv.adk2299-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/695f7ae5009c/sciadv.adk2299-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/8c64b79ca900/sciadv.adk2299-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/9170fd2cd9d5/sciadv.adk2299-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/d2d995cef93f/sciadv.adk2299-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/f5217fe70658/sciadv.adk2299-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/53de11d081e2/sciadv.adk2299-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/e9e9555ebb05/sciadv.adk2299-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bcb/11186505/a42f3922d111/sciadv.adk2299-f10.jpg

相似文献

[1]
In silico transcriptome screens identify epidermal growth factor receptor inhibitors as therapeutics for noise-induced hearing loss.

Sci Adv. 2024-6-21

[2]
In Silico Transcriptome-based Screens Identify Epidermal Growth Factor Receptor Inhibitors as Therapeutics for Noise-induced Hearing Loss.

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[3]
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[4]
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[10]
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引用本文的文献

[1]
GPR83 protects cochlear hair cells against ibrutinib-induced hearing loss through AKT signaling pathways.

Front Med (Lausanne). 2025-4-3

[2]
Paving the way for better ototoxicity assessments in cisplatin therapy using more reliable animal models.

Front Cell Neurosci. 2025-3-5

[3]
Occupational epidemiological characteristics of noise-induced hearing loss and the impact of combined exposure to noise and dust on workers' hearing-a retrospective study.

Front Public Health. 2024

[4]
Age-related hearing loss in older adults: etiology and rehabilitation strategies.

Front Neurosci. 2024-10-1

本文引用的文献

[1]
Hearing Loss Prevalence, Years Lived With Disability, and Hearing Aid Use in the United States From 1990 to 2019: Findings From the Global Burden of Disease Study.

Ear Hear.

[2]
Statins protect mice from high-decibel noise-induced hearing loss.

Biomed Pharmacother. 2023-7

[3]
Repurposing Drugs for the Treatment of COVID-19 and Its Cardiovascular Manifestations.

Circ Res. 2023-5-12

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Profiling mouse cochlear cell maturation using 10× Genomics single-cell transcriptomics.

Front Cell Neurosci. 2022-8-18

[5]
Drug Screening Approach Using L1000-Based Connectivity Map and Its Application to COVID-19.

Front Cardiovasc Med. 2022-3-24

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PLoS One. 2021

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Transl Psychiatry. 2021-11-16

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A cell-type-specific atlas of the inner ear transcriptional response to acoustic trauma.

Cell Rep. 2021-9-28

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Nucleic Acids Res. 2021-7-2

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Cell Death Dis. 2021-5-11

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