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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Frontiers Media S.A.
2020-02-01
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Online Access: | https://www.frontiersin.org/article/10.3389/fonc.2020.00101/full |
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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 |
work_keys_str_mv |
AT josephrtesta preclinicalmodelsofmalignantmesothelioma AT antonberns preclinicalmodelsofmalignantmesothelioma |
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