Wang Lei, Chen Huan, Fei Fei, He Xianfeng, Sun Shaoyang, Lv Kunpeng, Yu Bo, Long Jiang, Wang Xu
Department of Biochemistry and Molecular Biology, Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, School of Basic Medical Sciences, Fudan University.
National Human Genetic Resources Sharing Service Platform (2005DKA21300); Fudan University Shanghai Cancer Center.
J Vis Exp. 2019 Apr 30(146). doi: 10.3791/59507.
Patient-derived tumor xenograft (PDX) and cell-derived tumor xenograft (CDX) are important techniques for preclinical assessment, medication guidance and basic cancer researches. Generations of PDX models in traditional host mice are time-consuming and only working for a small proportion of samples. Recently, zebrafish PDX (zPDX) has emerged as a unique host system, with the characteristics of small-scale and high efficiency. Here, we describe an optimized methodology for generating a dual fluorescence-labeled tumor xenograft model for comparative chemotherapy assessment in zPDX models. Tumor cells and fibroblasts were enriched from freshly-harvested or frozen pancreatic cancer tissue at different culture conditions. Both cell groups were labeled by lentivirus expressing green or red fluorescent proteins, as well as an anti-apoptosis gene BCL2L1. The transfected cells were pre-mixed and co-injected into the 2 dpf larval zebrafish that were then bred in modified E3 medium at 32 °C. The xenograft models were treated by chemotherapy drugs and/or BCL2L1 inhibitor, and the viabilities of both tumor cells and fibroblasts were investigated simultaneously. In summary, this protocol allows researchers to quickly generate a large amount of zPDX models with a heterogeneous tumor microenvironment and provides a longer observation window and a more precise quantitation in assessing the efficiency of drug candidates.
患者来源的肿瘤异种移植(PDX)和细胞来源的肿瘤异种移植(CDX)是临床前评估、药物指导和基础癌症研究的重要技术。在传统宿主小鼠中建立多代PDX模型耗时且仅适用于一小部分样本。最近,斑马鱼PDX(zPDX)作为一种独特的宿主系统出现,具有小规模和高效率的特点。在此,我们描述了一种优化的方法,用于在zPDX模型中生成用于比较化疗评估的双荧光标记肿瘤异种移植模型。在不同培养条件下,从新鲜收获或冷冻的胰腺癌组织中富集肿瘤细胞和成纤维细胞。两组细胞均用表达绿色或红色荧光蛋白以及抗凋亡基因BCL2L1的慢病毒进行标记。将转染后的细胞预先混合并共同注射到2 dpf的斑马鱼幼体中,然后在32℃的改良E3培养基中饲养。用化疗药物和/或BCL2L1抑制剂处理异种移植模型,并同时研究肿瘤细胞和成纤维细胞的活力。总之,该方案使研究人员能够快速生成大量具有异质性肿瘤微环境的zPDX模型,并在评估候选药物效率时提供更长的观察窗口和更精确的定量。