Chang Wen-Hsin, Chin Andrew I, Chen Ching-Hsien
Division of Nephrology, Department of Internal Medicine, University of California, Davis, Davis, CA, USA; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, University of California, Davis, Davis, CA, USA; Comprehensive Cancer Center, University of California, Davis, Sacramento, CA, USA.
Division of Nephrology, Department of Internal Medicine, University of California, Davis, Davis, CA, USA.
STAR Protoc. 2025 Mar 21;6(1):103623. doi: 10.1016/j.xpro.2025.103623. Epub 2025 Feb 6.
Here, we present a protocol for a preclinical ex vivo platform combining experimental flexibility with preservation of the tumor microenvironment. We outline steps for isolating human peripheral blood mononuclear cells (PBMCs), preparing patient-derived precision-cut tumor slices (PCTSs), cryopreserving the samples, and setting up the co-culture system. We provide instructions for treatment applications, interactions, and analyzing therapy responses. By preserving tumor architecture and heterogeneity, this model is applicable for evaluating tumor characteristics, immune interactions, and treatment efficacy in translational cancer research.
在此,我们展示了一种临床前体外平台的方案,该平台将实验灵活性与肿瘤微环境的保存相结合。我们概述了分离人外周血单核细胞(PBMC)、制备患者来源的精密切割肿瘤切片(PCTS)、冷冻保存样本以及建立共培养系统的步骤。我们提供了治疗应用、相互作用和分析治疗反应的指导。通过保留肿瘤结构和异质性,该模型适用于评估转化癌症研究中的肿瘤特征、免疫相互作用和治疗效果。