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Secreted Factors from Human Vestibular Schwannomas Can Cause Cochlear Damage

Author(s)
Dilwali, Sonam; Landegger, Lukas D.; Soares, Vitor Y. R.; Deschler, Daniel G.; Stankovic, Konstantina M.
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Abstract
Vestibular schwannomas (VSs) are the most common tumours of the cerebellopontine angle. Ninety-five percent of people with VS present with sensorineural hearing loss (SNHL); the mechanism of this SNHL is currently unknown. To establish the first model to study the role of VS-secreted factors in causing SNHL, murine cochlear explant cultures were treated with human tumour secretions from thirteen different unilateral, sporadic VSs of subjects demonstrating varied degrees of ipsilateral SNHL. The extent of cochlear explant damage due to secretion application roughly correlated with the subjects’ degree of SNHL. Secretions from tumours associated with most substantial SNHL resulted in most significant hair cell loss and neuronal fibre disorganization. Secretions from VSs associated with good hearing or from healthy human nerves led to either no effect or solely fibre disorganization. Our results are the first to demonstrate that secreted factors from VSs can lead to cochlear damage. Further, we identified tumour necrosis factor alpha (TNFα) as an ototoxic molecule and fibroblast growth factor 2 (FGF2) as an otoprotective molecule in VS secretions. Antibody-mediated TNFα neutralization in VS secretions partially prevented hair cell loss due to the secretions. Taken together, we have identified a new mechanism responsible for SNHL due to VSs.
Date issued
2015-12
URI
http://hdl.handle.net/1721.1/100829
Department
Harvard University--MIT Division of Health Sciences and Technology
Journal
Scientific Reports
Publisher
Nature Publishing Group
Citation
Dilwali, Sonam, Lukas D. Landegger, Vitor Y. R. Soares, Daniel G. Deschler, and Konstantina M. Stankovic. “Secreted Factors from Human Vestibular Schwannomas Can Cause Cochlear Damage.” Scientific Reports 5 (December 22, 2015): 18599.
Version: Final published version
ISSN
2045-2322

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