Preclinical Models of Low-Grade Gliomas

Author:

Dasgupta Pushan1ORCID,Balasubramanyian Veerakumar2,de Groot John F.3,Majd Nazanin K.2

Affiliation:

1. Department of Neurology, Dell Medical School, University of Texas at Austin, Austin, TX 78712, USA

2. Department of Neuro-Oncology, UT MD Anderson Cancer Center, Houston, TX 77030, USA

3. Department of Neurosurgery, University of California San Francisco, San Francisco, CA 94143, USA

Abstract

Diffuse infiltrating low-grade glioma (LGG) is classified as WHO grade 2 astrocytoma with isocitrate dehydrogenase (IDH) mutation and oligodendroglioma with IDH1 mutation and 1p/19q codeletion. Despite their better prognosis compared with glioblastoma, LGGs invariably recur, leading to disability and premature death. There is an unmet need to discover new therapeutics for LGG, which necessitates preclinical models that closely resemble the human disease. Basic scientific efforts in the field of neuro-oncology are mostly focused on high-grade glioma, due to the ease of maintaining rapidly growing cell cultures and highly reproducible murine tumors. Development of preclinical models of LGG, on the other hand, has been difficult due to the slow-growing nature of these tumors as well as challenges involved in recapitulating the widespread genomic and epigenomic effects of IDH mutation. The most recent WHO classification of CNS tumors emphasizes the importance of the role of IDH mutation in the classification of gliomas, yet there are relatively few IDH-mutant preclinical models available. Here, we review the in vitro and in vivo preclinical models of LGG and discuss the mechanistic challenges involved in generating such models and potential strategies to overcome these hurdles.

Funder

Faculty Fund of N.K.M., Department of Neuro-Oncology, MD Anderson Cancer Center

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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