Formation of Human Neuroblastoma in Mouse-Human Neural Crest Chimeras

被引:35
作者
Cohen, Malkiel A. [1 ]
Zhang, Shupei [1 ]
Sengupta, Satyaki [2 ]
Ma, Haiting [1 ]
Bell, George W. [1 ]
Horton, Brendan [3 ]
Sharma, Bandana [2 ]
George, Rani E. [2 ]
Spranger, Stefani [3 ,4 ]
Jaenisch, Rudolf [1 ,4 ]
机构
[1] Whitehead Inst Biomed Res, 9 Cambridge Ctr, Cambridge, MA 02142 USA
[2] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA 02215 USA
[3] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
[4] MIT, Dept Biol, 77 Massachusetts Ave, Cambridge, MA 02142 USA
关键词
STEM-CELLS; ACTIVATING MUTATIONS; COLORECTAL TUMORS; ALK KINASE; N-MYC; EXPRESSION; MODEL; IDENTIFICATION; MECHANISMS; INJECTION;
D O I
10.1016/j.stem.2020.02.001
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Neuroblastoma (NB), derived from the neural crest (NC), is the most common pediatric extracranial solid tumor. Here, we establish a platform that allows the study of human NBs in mouse-human NC chimeras. Chimeric mice were produced by injecting human NC cells carrying NB relevant oncogenes in utero into gastrulating mouse embryos. The mice developed tumors composed of a heterogenous cell population that resembled that seen in primary NBs of patients but were significantly different from homogeneous tumors formed in xenotransplantation models. The human tumors emerged in immunocompetent hosts and were extensively infiltrated by mouse cytotoxic T cells, reflecting a vigorous host anti-tumor immune response. However, the tumors blunted the immune response by inducing infiltration of regulatory T cells and expression of immune-suppressive molecules similar to escape mechanisms seen in human cancer patients. Thus, this experimental platform allows the study of human tumor initiation, progression, manifestation, and tumor-immune-system interactions in an animal model system.
引用
收藏
页码:579 / +
页数:20
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