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Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone

Adenomatous tumors in the middle ear and temporal bone are rare but highly morbid because they are difficult to detect prior to the development of audiovestibular dysfunction. Complete resection is often disfiguring and difficult because of location and the late stage at diagnosis, so identification...

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Autores principales: Kawabata, Shigeru, Christine Hollander, M, Munasinghe, Jeeva P., Brinster, Lauren R., Mercado-Matos, José R., Li, Jie, Regales, Lucia, Pao, William, Jänne, Pasi A., Wong, Kwok-Kin, Butman, John A., Lonser, Russell R., Hansen, Marlan R., Gurgel, Richard K., Vortmeyer, Alexander O., Dennis, Phillip A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484461/
https://www.ncbi.nlm.nih.gov/pubmed/26027747
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author Kawabata, Shigeru
Christine Hollander, M
Munasinghe, Jeeva P.
Brinster, Lauren R.
Mercado-Matos, José R.
Li, Jie
Regales, Lucia
Pao, William
Jänne, Pasi A.
Wong, Kwok-Kin
Butman, John A.
Lonser, Russell R.
Hansen, Marlan R.
Gurgel, Richard K.
Vortmeyer, Alexander O.
Dennis, Phillip A.
author_facet Kawabata, Shigeru
Christine Hollander, M
Munasinghe, Jeeva P.
Brinster, Lauren R.
Mercado-Matos, José R.
Li, Jie
Regales, Lucia
Pao, William
Jänne, Pasi A.
Wong, Kwok-Kin
Butman, John A.
Lonser, Russell R.
Hansen, Marlan R.
Gurgel, Richard K.
Vortmeyer, Alexander O.
Dennis, Phillip A.
author_sort Kawabata, Shigeru
collection PubMed
description Adenomatous tumors in the middle ear and temporal bone are rare but highly morbid because they are difficult to detect prior to the development of audiovestibular dysfunction. Complete resection is often disfiguring and difficult because of location and the late stage at diagnosis, so identification of molecular targets and effective therapies is needed. Here, we describe a new mouse model of aggressive papillary ear tumor that was serendipitously discovered during the generation of a mouse model for mutant EGFR-driven lung cancer. Although these mice did not develop lung tumors, 43% developed head tilt and circling behavior. Magnetic resonance imaging (MRI) scans showed bilateral ear tumors located in the tympanic cavity. These tumors expressed mutant EGFR as well as active downstream targets such as Akt, mTOR and ERK1/2. EGFR-directed therapies were highly effective in eradicating the tumors and correcting the vestibular defects, suggesting these tumors are addicted to EGFR. EGFR activation was also observed in human ear neoplasms, which provides clinical relevance for this mouse model and rationale to test EGFR-targeted therapies in these rare neoplasms.
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spelling pubmed-44844612015-07-10 Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone Kawabata, Shigeru Christine Hollander, M Munasinghe, Jeeva P. Brinster, Lauren R. Mercado-Matos, José R. Li, Jie Regales, Lucia Pao, William Jänne, Pasi A. Wong, Kwok-Kin Butman, John A. Lonser, Russell R. Hansen, Marlan R. Gurgel, Richard K. Vortmeyer, Alexander O. Dennis, Phillip A. Oncotarget Research Paper Adenomatous tumors in the middle ear and temporal bone are rare but highly morbid because they are difficult to detect prior to the development of audiovestibular dysfunction. Complete resection is often disfiguring and difficult because of location and the late stage at diagnosis, so identification of molecular targets and effective therapies is needed. Here, we describe a new mouse model of aggressive papillary ear tumor that was serendipitously discovered during the generation of a mouse model for mutant EGFR-driven lung cancer. Although these mice did not develop lung tumors, 43% developed head tilt and circling behavior. Magnetic resonance imaging (MRI) scans showed bilateral ear tumors located in the tympanic cavity. These tumors expressed mutant EGFR as well as active downstream targets such as Akt, mTOR and ERK1/2. EGFR-directed therapies were highly effective in eradicating the tumors and correcting the vestibular defects, suggesting these tumors are addicted to EGFR. EGFR activation was also observed in human ear neoplasms, which provides clinical relevance for this mouse model and rationale to test EGFR-targeted therapies in these rare neoplasms. Impact Journals LLC 2015-03-15 /pmc/articles/PMC4484461/ /pubmed/26027747 Text en Copyright: © 2015 Kawabata et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Kawabata, Shigeru
Christine Hollander, M
Munasinghe, Jeeva P.
Brinster, Lauren R.
Mercado-Matos, José R.
Li, Jie
Regales, Lucia
Pao, William
Jänne, Pasi A.
Wong, Kwok-Kin
Butman, John A.
Lonser, Russell R.
Hansen, Marlan R.
Gurgel, Richard K.
Vortmeyer, Alexander O.
Dennis, Phillip A.
Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone
title Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone
title_full Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone
title_fullStr Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone
title_full_unstemmed Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone
title_short Epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone
title_sort epidermal growth factor receptor as a novel molecular target for aggressive papillary tumors in the middle ear and temporal bone
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484461/
https://www.ncbi.nlm.nih.gov/pubmed/26027747
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