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Preclinical Models of Malignant Mesothelioma

Rodent models of malignant mesothelioma help facilitate the understanding of the biology of this highly lethal cancer and to develop and test new interventions. Introducing the same genetic lesions as found in human mesothelioma in mice results in tumors that show close resemblance with the human di...

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Autores principales: Testa, Joseph R., Berns, Anton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026500/
https://www.ncbi.nlm.nih.gov/pubmed/32117751
http://dx.doi.org/10.3389/fonc.2020.00101
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author Testa, Joseph R.
Berns, Anton
author_facet Testa, Joseph R.
Berns, Anton
author_sort Testa, Joseph R.
collection PubMed
description Rodent models of malignant mesothelioma help facilitate the understanding of the biology of this highly lethal cancer and to develop and test new interventions. Introducing the same genetic lesions as found in human mesothelioma in mice results in tumors that show close resemblance with the human disease counterpart. This includes the extensive inflammatory responses that characterize human malignant mesothelioma. The relatively fast development of mesothelioma in mice when the appropriate combination of lesions is introduced, with or without exposure to asbestos, make the autochthonous models particularly useful for testing new treatment strategies in an immunocompetent setting, whereas Patient-Derived Xenograft models are particularly useful to assess effects of inter- and intra-tumor heterogeneity and human-specific features of mesothelioma. It is to be expected that new insights obtained by studying these experimental systems will lead to new more effective treatments for this devastating disease.
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spelling pubmed-70265002020-02-28 Preclinical Models of Malignant Mesothelioma Testa, Joseph R. Berns, Anton Front Oncol Oncology Rodent models of malignant mesothelioma help facilitate the understanding of the biology of this highly lethal cancer and to develop and test new interventions. Introducing the same genetic lesions as found in human mesothelioma in mice results in tumors that show close resemblance with the human disease counterpart. This includes the extensive inflammatory responses that characterize human malignant mesothelioma. The relatively fast development of mesothelioma in mice when the appropriate combination of lesions is introduced, with or without exposure to asbestos, make the autochthonous models particularly useful for testing new treatment strategies in an immunocompetent setting, whereas Patient-Derived Xenograft models are particularly useful to assess effects of inter- and intra-tumor heterogeneity and human-specific features of mesothelioma. It is to be expected that new insights obtained by studying these experimental systems will lead to new more effective treatments for this devastating disease. Frontiers Media S.A. 2020-02-11 /pmc/articles/PMC7026500/ /pubmed/32117751 http://dx.doi.org/10.3389/fonc.2020.00101 Text en Copyright © 2020 Testa and Berns. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Testa, Joseph R.
Berns, Anton
Preclinical Models of Malignant Mesothelioma
title Preclinical Models of Malignant Mesothelioma
title_full Preclinical Models of Malignant Mesothelioma
title_fullStr Preclinical Models of Malignant Mesothelioma
title_full_unstemmed Preclinical Models of Malignant Mesothelioma
title_short Preclinical Models of Malignant Mesothelioma
title_sort preclinical models of malignant mesothelioma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026500/
https://www.ncbi.nlm.nih.gov/pubmed/32117751
http://dx.doi.org/10.3389/fonc.2020.00101
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