癌变
免疫疗法
生物
脑瘤
癌症
免疫系统
癌症研究
胶质瘤
胶质母细胞瘤
神经科学
免疫学
医学
生物信息学
病理
遗传学
作者
John Figg,Dongjiang Chen,Laura Falceto Font,Catherine Flores,Dan Jin
出处
期刊:Neuro-oncology
[Oxford University Press]
日期:2024-07-11
标识
DOI:10.1093/neuonc/noae131
摘要
Abstract Brain tumors, particularly glioblastoma (GBM), are devastating and challenging to treat, with a low 5-year survival rate of only 6.6%. Mouse models are established to understand tumorigenesis and develop new therapeutic strategies. Large-scale genomic studies have facilitated the identification of genetic alterations driving human brain tumor development and progression. Genetically engineered mouse models (GEMMs) with clinically relevant genetic alterations are widely used to investigate tumor origin. Additionally, syngeneic implantation models, utilizing cell lines derived from GEMMs or other sources, are popular for their consistent and relatively short latency period, addressing various brain cancer research questions. In recent years, the success of immunotherapy in specific cancer types has led to a surge in cancer immunology-related research which specifically necessitates the utilization of immunocompetent mouse models. In this review, we provide a comprehensive summary of GEMMs and syngeneic mouse models for adult brain tumors, emphasizing key features such as model origin, genetic alteration background, oncogenic mechanisms, and immune-related characteristics. Our review serves as a valuable resource for the brain tumor research community, aiding in the selection of appropriate models to study cancer immunology.
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