The Zebrafish Xenograft Platform: Evolution of a Novel Cancer Model and Preclinical Screening Tool

被引:54
作者
Wertman, Jaime [1 ]
Veinotte, Chansey J. [2 ]
Dellaire, Graham [3 ]
Berman, Jason N. [1 ,2 ]
机构
[1] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 4R2, Canada
[2] IWK Hlth Ctr, Dept Pediat, Halifax, NS, Canada
[3] Dalhousie Univ, Dept Pathol, Halifax, NS, Canada
来源
CANCER AND ZEBRAFISH: MECHANISMS, TECHNIQUES, AND MODELS | 2016年 / 916卷
关键词
Zebrafish; Xenotransplant; Xenograft; Cancer; Model organism; IN-VIVO; METASTATIC BEHAVIOR; DRUG DISCOVERY; IMMUNE-SYSTEM; XENOTRANSPLANTATION; CELLS; MICE; ANGIOGENESIS; MELANOMA; TRANSPLANTATION;
D O I
10.1007/978-3-319-30654-4_13
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Animal xenografts of human cancers represent a key preclinical tool in the field of cancer research. While mouse xenografts have long been the gold standard, investigators have begun to use zebrafish (Danio rerio) xenotransplantation as a relatively rapid, robust and cost-effective in vivo model of human cancers. There are several important methodological considerations in the design of an informative and efficient zebrafish xenotransplantation experiment. Various transgenic fish strains have been created that facilitate microscopic observation, ranging from the completely transparent casper fish to the Tg(fli1:eGFP) fish that expresses fluorescent GFP protein in its vascular tissue. While human cancer cell lines have been used extensively in zebrafish xenotransplantation studies, several reports have also used primary patient samples as the donor material. The zebrafish is ideally suited for transplanting primary patient material by virtue of the relatively low number of cells required for each embryo (between 50 and 300 cells), the absence of an adaptive immune system in the early zebrafish embryo, and the short experimental time-frame (5-7 days). Following xenotransplantation into the fish, cells can be tracked using in vivo or ex vivo measures of cell proliferation and migration, facilitated by fluorescence or human-specific protein expression. Importantly, assays have
引用
收藏
页码:289 / 314
页数:26
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