Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California.
Curr Protoc. 2023 Feb;3(2):e665. doi: 10.1002/cpz1.665.
Research models in cancer have greatly evolved in the last decade, with the advent of several new methods both in vitro and in vivo. While in vivo models remain the gold standard for preclinical studies, these methods present a series of disadvantages such as a high cost and long periods of time to produce results compared with in vitro models. We have previously developed a method named Mosaic Analysis by Dual Recombinase-mediated cassette exchange (MADR) that generates autochthonous gliomas in immunocompetent mice through the transgenesis of personalized driver mutations, which highly mimic the spatial and temporal tumor development of their human counterparts. Due to the control of single-copy expression of transgenes, it allows for comparing the visualization of tumor cells and non-tumor cells. Here we describe a method to generate murine-derived glioma organoids (MGOs) and cell line cultures from these murine models by physical and enzymatic methods for in vitro downstream applications. Tumor cells can be readily distinguished from non-tumor cell populations, in both organoids and monolayer cell cultures, and isolated due to the use of personalized fluorescent reporter transgenes. © 2023 Wiley Periodicals LLC. Basic Protocol 1: Generation of 3D murine-derived glioma organoids Basic Protocol 2: Generation of 2D glioma monolayer cell lines.
在过去的十年中,癌症研究模型有了很大的发展,无论是在体外还是体内,都出现了几种新方法。虽然体内模型仍然是临床前研究的金标准,但与体外模型相比,这些方法存在一系列缺点,例如成本高、产生结果的时间长。我们之前开发了一种名为双重组酶介导的盒式交换马赛克分析(MADR)的方法,通过对个性化驱动突变的转基因,在免疫功能正常的小鼠中产生同源性神经胶质瘤,高度模拟了人类肿瘤的时空发展。由于转基因的单拷贝表达得到控制,因此可以比较肿瘤细胞和非肿瘤细胞的可视化。在这里,我们描述了一种通过物理和酶方法从这些小鼠模型中生成鼠源性神经胶质瘤类器官(MGOs)和细胞系培养物的方法,用于体外下游应用。由于使用了个性化的荧光报告转基因,肿瘤细胞可以很容易地与类器官和单层细胞培养物中的非肿瘤细胞群体区分开来,并进行分离。©2023 威利父子公司。基础方案 1:生成 3D 鼠源性神经胶质瘤类器官基础方案 2:生成 2D 神经胶质瘤单层细胞系。