TY - JOUR
T1 - Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research
AU - Sahu, Upasana
AU - Barth, Rolf F.
AU - Otani, Yoshihiro
AU - McCormack, Ryan
AU - Kaur, Balveen
N1 - Funding Information:
BK received support from the National Cancer Institute, PO1 CA163205, and National Institute of Neurological Disorders and Stroke, R61 NS112410 and RO1 NS127473. RFB received support from the National Cancer Institute, 1RO1 CA098945-01, 1RO1 CA129326, and 1RO1 CA127935, Voices Against Brain Cancer, the Musella Foundation, and the Kevin Mullin Memorial Fund for Brain Tumor Research. RFB gratefully thanks David Carpenter for outstanding assistance in the preparation of this review.
Publisher Copyright:
© 2022 The Author(s) 2022. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc.
PY - 2022/5/1
Y1 - 2022/5/1
N2 - 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.
AB - 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.
KW - 9L
KW - C6
KW - F98 rat brain tumor models
KW - Genetically engineered and humanized mouse brain models
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U2 - 10.1093/jnen/nlac021
DO - 10.1093/jnen/nlac021
M3 - Review article
C2 - 35446393
AN - SCOPUS:85130646069
SN - 0002-9564
VL - 81
JO - Journal of Psychotherapy Practice and Research
JF - Journal of Psychotherapy Practice and Research
IS - 5
M1 - nlac021
ER -