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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Main Authors: Joseph R. Testa, Anton Berns
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2020.00101/full
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spelling doaj-41ee6425526d4a5ab8670487c7f2bb4d2020-11-24T20:57:45ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2020-02-011010.3389/fonc.2020.00101505600Preclinical Models of Malignant MesotheliomaJoseph R. Testa0Anton Berns1Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, PA, United StatesDivision of Molecular Genetics, The Netherlands Cancer Institute, Amsterdam, NetherlandsRodent 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.https://www.frontiersin.org/article/10.3389/fonc.2020.00101/fullmalignant mesotheliomapreclinical rodent modelsin vivo asbestos carcinogenesisgenetic driver lesionsmesothelioma inflammatory phenotypeconditional tumor suppressor gene knockout/oncogene mouse models
collection DOAJ
language English
format Article
sources DOAJ
author Joseph R. Testa
Anton Berns
spellingShingle Joseph R. Testa
Anton Berns
Preclinical Models of Malignant Mesothelioma
Frontiers in Oncology
malignant mesothelioma
preclinical rodent models
in vivo asbestos carcinogenesis
genetic driver lesions
mesothelioma inflammatory phenotype
conditional tumor suppressor gene knockout/oncogene mouse models
author_facet Joseph R. Testa
Anton Berns
author_sort Joseph R. Testa
title Preclinical Models of Malignant Mesothelioma
title_short 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_sort preclinical models of malignant mesothelioma
publisher Frontiers Media S.A.
series Frontiers in Oncology
issn 2234-943X
publishDate 2020-02-01
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.
topic malignant mesothelioma
preclinical rodent models
in vivo asbestos carcinogenesis
genetic driver lesions
mesothelioma inflammatory phenotype
conditional tumor suppressor gene knockout/oncogene mouse models
url https://www.frontiersin.org/article/10.3389/fonc.2020.00101/full
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