| Literature DB >> 32142683 |
Malkiel A Cohen1, Shupei Zhang1, Satyaki Sengupta2, Haiting Ma1, George W Bell1, Brendan Horton3, Bandana Sharma2, Rani E George4, Stefani Spranger5, Rudolf Jaenisch6.
Abstract
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.Entities:
Keywords: cancer model; immune evasion; interspecies chimeras; neural crest; neuroblastoma; pluripotent stem cells
Mesh:
Year: 2020 PMID: 32142683 PMCID: PMC7663823 DOI: 10.1016/j.stem.2020.02.001
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633