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Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research
Rodent brain tumor models have been useful for developing effective therapies for glioblastomas (GBMs). In this review, we first discuss the 3 most commonly used rat brain tumor models, the C6, 9L, and F98 gliomas, which are all induced by repeated injections of nitrosourea to adult rats. The C6 gli...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113334/ https://www.ncbi.nlm.nih.gov/pubmed/35446393 http://dx.doi.org/10.1093/jnen/nlac021 |
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author | Sahu, Upasana Barth, Rolf F Otani, Yoshihiro McCormack, Ryan Kaur, Balveen |
author_facet | Sahu, Upasana Barth, Rolf F Otani, Yoshihiro McCormack, Ryan Kaur, Balveen |
author_sort | Sahu, Upasana |
collection | PubMed |
description | Rodent brain tumor models have been useful for developing effective therapies for glioblastomas (GBMs). In this review, we first discuss the 3 most commonly used rat brain tumor models, the C6, 9L, and F98 gliomas, which are all induced by repeated injections of nitrosourea to adult rats. The C6 glioma arose in an outbred Wistar rat and its potential to evoke an alloimmune response is a serious limitation. The 9L gliosarcoma arose in a Fischer rat and is strongly immunogenic, which must be taken into consideration when using it for therapy studies. The F98 glioma may be the best of the 3 but it does not fully recapitulate human GBMs because it is weakly immunogenic. Next, we discuss a number of mouse models. The first are human patient-derived xenograft gliomas in immunodeficient mice. These have failed to reproduce the tumor-host interactions and microenvironment of human GBMs. Genetically engineered mouse models recapitulate the molecular alterations of GBMs in an immunocompetent environment and “humanized” mouse models repopulate with human immune cells. While the latter are rarely isogenic, expensive to produce, and challenging to use, they represent an important advance. The advantages and limitations of each of these brain tumor models are discussed. This information will assist investigators in selecting the most appropriate model for the specific focus of their research. |
format | Online Article Text |
id | pubmed-9113334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91133342022-05-18 Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research Sahu, Upasana Barth, Rolf F Otani, Yoshihiro McCormack, Ryan Kaur, Balveen J Neuropathol Exp Neurol Invited Review Article Rodent brain tumor models have been useful for developing effective therapies for glioblastomas (GBMs). In this review, we first discuss the 3 most commonly used rat brain tumor models, the C6, 9L, and F98 gliomas, which are all induced by repeated injections of nitrosourea to adult rats. The C6 glioma arose in an outbred Wistar rat and its potential to evoke an alloimmune response is a serious limitation. The 9L gliosarcoma arose in a Fischer rat and is strongly immunogenic, which must be taken into consideration when using it for therapy studies. The F98 glioma may be the best of the 3 but it does not fully recapitulate human GBMs because it is weakly immunogenic. Next, we discuss a number of mouse models. The first are human patient-derived xenograft gliomas in immunodeficient mice. These have failed to reproduce the tumor-host interactions and microenvironment of human GBMs. Genetically engineered mouse models recapitulate the molecular alterations of GBMs in an immunocompetent environment and “humanized” mouse models repopulate with human immune cells. While the latter are rarely isogenic, expensive to produce, and challenging to use, they represent an important advance. The advantages and limitations of each of these brain tumor models are discussed. This information will assist investigators in selecting the most appropriate model for the specific focus of their research. Oxford University Press 2022-04-21 /pmc/articles/PMC9113334/ /pubmed/35446393 http://dx.doi.org/10.1093/jnen/nlac021 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Review Article Sahu, Upasana Barth, Rolf F Otani, Yoshihiro McCormack, Ryan Kaur, Balveen Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research |
title | Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research |
title_full | Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research |
title_fullStr | Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research |
title_full_unstemmed | Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research |
title_short | Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research |
title_sort | rat and mouse brain tumor models for experimental neuro-oncology research |
topic | Invited Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113334/ https://www.ncbi.nlm.nih.gov/pubmed/35446393 http://dx.doi.org/10.1093/jnen/nlac021 |
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