Chadwick Emily J, Yang David P, Filbin Mariella G, Mazzola Emanuele, Sun Yu, Behar Oded, Pazyra-Murphy Maria F, Goumnerova Liliana, Ligon Keith L, Stiles Charles D, Segal Rosalind A
Department of Cancer Biology, Dana-Farber Cancer Institute.
Department of Pediatrics, Children's Hospital.
J Vis Exp. 2015 Nov 7(105):e53304. doi: 10.3791/53304.
Brain tumors are a major cause of cancer-related morbidity and mortality. Developing new therapeutics for these cancers is difficult, as many of these tumors are not easily grown in standard culture conditions. Neurosphere cultures under serum-free conditions and orthotopic xenografts have expanded the range of tumors that can be maintained. However, many types of brain tumors remain difficult to propagate or study. This is particularly true for pediatric brain tumors such as pilocytic astrocytomas and medulloblastomas. This protocol describes a system that allows primary human brain tumors to be grown in culture. This quantitative assay can be used to investigate the effect of microenvironment on tumor growth, and to test new drug therapies. This protocol describes a system where fluorescently labeled brain tumor cells are grown on an organotypic brain slice from a juvenile mouse. The response of tumor cells to drug treatments can be studied in this assay, by analyzing changes in the number of cells on the slice over time. In addition, this system can address the nature of the microenvironment that normally fosters growth of brain tumors. This brain tumor organotypic slice co-culture assay provides a propitious system for testing new drugs on human tumor cells within a brain microenvironment.
脑肿瘤是癌症相关发病和死亡的主要原因。开发针对这些癌症的新疗法很困难,因为许多此类肿瘤在标准培养条件下不易生长。无血清条件下的神经球培养和原位异种移植扩大了可维持的肿瘤范围。然而,许多类型的脑肿瘤仍然难以繁殖或研究。对于小儿脑肿瘤,如毛细胞型星形细胞瘤和髓母细胞瘤,尤其如此。本方案描述了一种能使原发性人脑肿瘤在培养中生长的系统。这种定量测定可用于研究微环境对肿瘤生长的影响,并测试新的药物疗法。本方案描述了一种系统,其中荧光标记的脑肿瘤细胞在幼年小鼠的器官型脑切片上生长。通过分析切片上细胞数量随时间的变化,可在该测定中研究肿瘤细胞对药物治疗的反应。此外,该系统可以揭示通常促进脑肿瘤生长的微环境的性质。这种脑肿瘤器官型切片共培养测定为在脑微环境中对人类肿瘤细胞测试新药提供了一个有利的系统。