Hooking the big one: the potential of zebrafish xenotransplantation to reform cancer drug screening in the genomic era

被引:129
作者
Veinotte, Chansey J. [1 ,2 ]
Dellaire, Graham [3 ]
Berman, Jason N. [1 ,2 ,3 ,4 ]
机构
[1] IWK Hlth Ctr, Dept Pediat, Halifax, NS B3K 6R8, Canada
[2] Dalhousie Univ, Fac Med, Life Sci Res Inst, Halifax, NS B3H 4R2, Canada
[3] Dalhousie Univ, Dept Pathol, Halifax, NS B3H 4R2, Canada
[4] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
Cancer; Drug screening; Microenvironment; Xenotransplantation; Zebrafish; CHEMICAL GENETIC SCREEN; IN-VIVO; SMALL MOLECULES; METASTATIC BEHAVIOR; TUMOR ANGIOGENESIS; TRANSGENIC MODEL; MOUSE MODELS; CELLS; ASSAY; XENOGRAFTS;
D O I
10.1242/dmm.015784
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The current preclinical pipeline for drug discovery can be cumbersome and costly, which limits the number of compounds that can effectively be transitioned to use as therapies. Chemical screens in zebrafish have uncovered new uses for existing drugs and identified promising new compounds from large libraries. Xenotransplantation of human cancer cells into zebrafish embryos builds on this work and enables direct evaluation of patient-derived tumor specimens in vivo in a rapid and cost-effective manner. The short time frame needed for xenotransplantation studies means that the zebrafish can serve as an early preclinical drug screening tool and can also help personalize cancer therapy by providing real-time data on the response of the human cells to treatment. In this Review, we summarize the use of zebrafish embryos in drug screening and highlight the potential for xenotransplantation approaches to be adopted as a preclinical tool to identify and prioritize therapies for further clinical evaluation. We also discuss some of the limitations of using zebrafish xenografts and the benefits of using them in concert with murine xenografts in drug optimization.
引用
收藏
页码:745 / 754
页数:10
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