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基于转录组学的药物重用来治疗与年龄相关的听力损失

Transcriptome-Guided Identification of Drugs for Repurposing to Treat Age-Related Hearing Loss.

机构信息

Department of Otorhinolaryngology and Head and Neck Surgery, University Medical Center Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands.

Graduate School of Medical Sciences Research School of Behavioural and Cognitive Neurosciences, University of Groningen, 9713 AV Groningen, The Netherlands.

出版信息

Biomolecules. 2022 Mar 25;12(4):498. doi: 10.3390/biom12040498.

Abstract

Age-related hearing loss (ARHL) or presbycusis is a prevalent condition associated with social isolation, cognitive impairment, and dementia. Age-related changes in the cochlea, the auditory portion of the inner ear, are the primary cause of ARHL. Unfortunately, there are currently no pharmaceutical approaches to treat ARHL. To examine the biological processes underlying age-related changes in the cochlea and identify candidate drugs for rapid repurposing to treat ARHL, we utilized bulk RNA sequencing to obtain transcriptomes from the functional substructures of the cochlea-the sensorineural structures, including the organ of Corti and spiral ganglion neurons (OC/SGN) and the stria vascularis and spiral ligament (SV/SL)-in young (6-week-old) and old (2-year-old) C57BL/6 mice. Transcriptomic analyses revealed both overlapping and unique patterns of gene expression and gene enrichment between substructures and with ageing. Based on these age-related transcriptional changes, we queried the protein products of genes differentially expressed with ageing in DrugBank and identified 27 FDA/EMA-approved drugs that are suitable to be repurposed to treat ARHL. These drugs target the protein products of genes that are differentially expressed with ageing uniquely in either the OC/SGN or SV/SL and that interrelate diverse biological processes. Further transcriptomic analyses revealed that most genes differentially expressed with ageing in both substructures encode protein products that are promising drug target candidates but are, nevertheless, not yet linked to approved drugs. Thus, with this study, we apply a novel approach to characterize the druggable genetic landscape for ARHL and propose a list of drugs to test in pre-clinical studies as potential treatment options for ARHL.

摘要

年龄相关性听力损失(ARHL)或老年性聋是一种与社会隔离、认知障碍和痴呆相关的常见疾病。内耳听觉部分耳蜗的年龄相关性变化是 ARHL 的主要原因。不幸的是,目前尚无药物治疗 ARHL 的方法。为了研究耳蜗年龄相关性变化的生物学过程,并确定候选药物用于快速重新用于治疗 ARHL,我们利用批量 RNA 测序从耳蜗的功能亚结构-包括感觉神经元结构(OC/SGN)和血管纹和螺旋韧带(SV/SL)-获得年轻(6 周龄)和老年(2 岁)C57BL/6 小鼠的转录组。转录组分析显示,亚结构之间以及与年龄相关的基因表达和基因富集既有重叠又有独特的模式。基于这些与年龄相关的转录变化,我们在 DrugBank 中查询了与年龄相关的基因表达差异的蛋白质产物,并确定了 27 种 FDA/EMA 批准的药物可重新用于治疗 ARHL。这些药物针对的是在 OC/SGN 或 SV/SL 中与年龄相关的基因的蛋白质产物表达差异,并且与多种生物学过程相关。进一步的转录组分析表明,在这两个亚结构中与年龄相关的大多数基因差异表达都编码有希望成为药物靶点的蛋白质产物,但尚未与已批准的药物相关联。因此,通过这项研究,我们应用一种新方法来描述 ARHL 的可药物治疗遗传景观,并提出了一系列药物在临床前研究中作为 ARHL 的潜在治疗选择进行测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1711/9028743/5c7444f94d72/biomolecules-12-00498-g001.jpg

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