The Molecular Biology of Vestibular Schwannomas and Its Association with Hearing Loss: A Review

Author:

Celis-Aguilar Erika1,Lassaletta Luis2,Torres-Martín Miguel3,Rodrigues F. Yuri4,Nistal Manuel4,Castresana Javier S.5,Gavilan Javier2,Rey Juan A.4

Affiliation:

1. Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suarez, 14269 Ciudad de México, DF, Mexico

2. Department of Otolaryngology, “La Paz” University Hospital, 28046 Madrid, Spain

3. Unidad de Investigación, Laboratorio Oncogenetica Molecular, “La Paz” University Hospital, 28046 Madrid, Spain

4. Department of Pathology, “La Paz” University Hospital, 28046 Madrid, Spain

5. Brain Tumor Biology Unit, CIFA, University of Navarra School of Sciences, 31009 Pamplona, Spain

Abstract

Hearing loss is the most common symptom in patients with vestibular schwannoma (VS). In the past, compressive mechanisms caused by the tumoral mass and its growth have been regarded as the most likely causes of the hearing loss associated with VS. Interestingly, new evidence proposes molecular mechanisms as an explanation for such hearing loss. Among the molecular mechanisms proposed are methylation of TP73, negative expression of cyclin D1, expression of B7-H1, increased expression of the platelet-derived growth factor A, underexpression of PEX5L, RAD54B, and PSMAL, and overexpression of CEA. Many molecular mechanisms are involved in vestibular schwannoma development; we review some of these mechanisms with special emphasis on hearing loss associated with vestibular schwannoma.

Publisher

Hindawi Limited

Subject

Genetics (clinical),Genetics,Molecular Biology

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