发布: 2017年07月20日第7卷第14期 DOI: 10.21769/BioProtoc.2404 浏览次数: 9878
评审: Emilie ViennoisKathrin SutterAnonymous reviewer(s)
Abstract
Glioblastoma (GBM) is the most common primary brain cancer in adults and has a poor prognosis. It is characterized by a high degree of cellular infiltration that leads to tumor recurrence, atypical hyperplasia, necrosis, and angiogenesis. Despite aggressive treatment modalities, current therapies are ineffective for GBM. Mouse GBM models not only provide a better understanding in the mechanisms of gliomagenesis, but also facilitate the drug discovery for treating this deadly cancer. A retroviral vector system that expresses PDGFBB (Platelet-derived growth factor BB) and inactivates PTEN (Phosphatase and tensin homolog) and P53 tumor suppressors provides a rapid and efficient induction of glioma in mice with full penetrance. In this protocol, we describe a simple and practical method for inducing GBM formation by retrovirus injection in the murine brain. This system gives a spatial and temporal control over the induction of glioma and allows the assessment of therapeutic effects with a bioluminescent reporter.
Keywords: Glioma (胶质瘤)Background
Glioblastoma (GBM) is the most aggressive malignant brain tumor and unfortunately is also almost always fatal. Despite advances in multiple therapeutic modalities, no effective therapy has been developed to cure GBM. The mechanisms underlying this disease remain poorly understood. Animal models have been a very important tool to define the GBM pathogenesis and test for gene or drug therapeutics. Several mouse models have been developed with the aim to produce a disease which mimics the human disease as closely as possible and exhibits similar molecular, genetic and histological character. The prominently used models are xenograft (Hingtgen et al., 2008) models where human tumor cell lines can be transplanted orthotopically in brain as well as ectopically in subcutaneous area in immunocompromised mice, providing an advantage of having a large tumor mass in a brief period. Genetically engineered mice models (GEMM) with specific gain-of oncogenic activities or loss of tumor suppressor pathways, which resemble perturbations in the most frequently dysregulated pathways in GBM, results in formation of gliomas in rodents. Genetic perturbations in GEMM models often include the gain-of-function mutations in oncogenic factors such as EGFR, PI-3K, and Ras (Holland et al., 2000; Zhu et al., 2009), and PDGF amplification (Assanah et al., 2006), as well as the loss-of-function in tumor suppressors such as NF1 (Zhu et al., 2005), TP53 (p53) (Zheng et al., 2008), Ink4a/ARF (Holland, 2001), PTEN (Holland et al., 1998 and 2000). The use of viral vectors (Ikawa et al., 2003; Hambardzumyan et al., 2009; Marumoto et al., 2009; Friedmann-Morvinski et al., 2012) such as retrovirus, lentivirus and adenovirus carrying oncogenes and/or targeting tumor suppressors has been a convenient and effective approach to induce brain tumor formation in rodents. There is a need for testing multiple different tumor models for therapeutics since different subtypes of gliomas have varied genetic profiles and clinical responses to drug treatment.
GBM have been classified into four subtypes depending upon their gene expression pattern and molecular signature, namely, Mesenchymal, Neural, Proneural and Classical tumors (Verhaak et al., 2010). The Proneural subtype of GBM predominantly involves mutations/loss in oncogene P53 and amplification of PDGFRα with loss of PTEN seen across all the subtypes (Verhaak et al., 2010; Lei et al., 2011). To closely imitate the human Proneural subtype, Lei et al. (2011) devised a GBM model by inducing PTEN and P53 deletion and PDGFBB overexpression in the progenitor cells of the white matter region of adult murine brain through retrovirus inoculation (Lei et al., 2011). We have successfully used this retrovirus-induced GBM model in mice ranging in age from day 2 to 3-month-old adult mice with remarkable reproducibility (Lu et al., 2016). This model develops gliomas with full penetrance within 3-4 weeks which in contrast to other GEMM models, which take a significantly longer time.
Materials and Reagents
Note: We use a two-vector system for retrovirus production. One is a retroviral vector carrying PDGFB-IRES-Cre, which overexpresses PDGFB and Cre, and another is a retroviral packaging plasmid, which provides gag, pol and env to produce VSV-G pseudotyped retrovirus. We use commercially available DNA transfection reagents for 293T HEK transfection to produce the retrovirus.
Equipment
Procedure
文章信息
版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Verma, R. K., Lu, F. and Lu, Q. R. (2017). Glioma Induction by Intracerebral Retrovirus Injection. Bio-protocol 7(14): e2404. DOI: 10.21769/BioProtoc.2404.
分类
癌症生物学 > 通用技术 > 动物模型
癌症生物学 > 肿瘤免疫学 > 动物模型
细胞生物学 > 组织分析 > 组织分离
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