Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Mayo Clinic Cancer Center.
Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Mayo Clinic Cancer Center;
J Vis Exp. 2021 Mar 14(169). doi: 10.3791/62416.
Zebrafish has emerged as an important animal model to study human diseases, especially cancer. Along with the robust transgenic and genome editing technologies applied in zebrafish modeling, the ease of maintenance, high-yield productivity, and powerful live imaging altogether make the zebrafish a valuable model system to study metastasis and cellular and molecular bases underlying this process in vivo. The first zebrafish neuroblastoma (NB) model of metastasis was developed by overexpressing two oncogenes, MYCN and LMO1, under control of the dopamine-beta-hydroxylase (dβh) promoter. Co-overexpressed MYCN and LMO1 led to the reduced latency and increased penetrance of neuroblastomagenesis, as well as accelerated distant metastasis of tumor cells. This new model reliably reiterates many key features of human metastatic NB, including involvement of clinically relevant and metastasis-associated genetic alterations; natural and spontaneous development of metastasis in vivo; and conserved sites of metastases. Therefore, the zebrafish model possesses unique advantages to dissect the complex process of tumor metastasis in vivo.
斑马鱼已成为研究人类疾病(尤其是癌症)的重要动物模型。随着在斑马鱼模型中应用的强大的转基因和基因组编辑技术,以及易于维持、高产、强大的活体成像,斑马鱼成为研究转移以及体内这一过程的细胞和分子基础的有价值的模型系统。通过多巴胺-β-羟化酶(dβh)启动子控制下过表达两个癌基因 MYCN 和 LMO1,首次建立了斑马鱼神经母细胞瘤(NB)转移模型。共过表达 MYCN 和 LMO1 导致神经母细胞瘤发生的潜伏期缩短、穿透性增加,以及肿瘤细胞的远处转移加速。该新型模型可靠地重复了许多人类转移性 NB 的关键特征,包括涉及临床相关和转移相关遗传改变;体内转移的自然和自发性发展;以及转移部位的保守性。因此,斑马鱼模型具有独特的优势,可以在体内解析肿瘤转移的复杂过程。