Establishment of Gastric Cancer Patient-derived Xenograft Models and Primary Cell Lines

癌症 体内 癌细胞 癌症研究 医学 肿瘤微环境 癌细胞系 细胞培养 原发性肿瘤 生物 计算生物学 内科学 转移 遗传学 生物技术
作者
Jiahuan Lu,Yun Wang,Qi Meng,Zhao-Lei Zeng
出处
期刊:Journal of Visualized Experiments [MyJOVE]
卷期号: (149) 被引量:5
标识
DOI:10.3791/59871
摘要

The use of preclinical models to advance our understanding of tumor biology and investigate the efficacy of therapeutic agents is key to cancer research. Although there are many established gastric cancer cell lines and many conventional transgenic mouse models for preclinical research, the disadvantages of these in vitro and in vivo models limit their applications. Because the characteristics of these models have changed in culture, they no longer model tumor heterogeneity, and their responses have not been able to predict responses in humans. Thus, alternative models that better represent tumor heterogeneity are being developed. Patient-derived xenograft (PDX) models preserve the histologic appearance of cancer cells, retain intratumoral heterogeneity, and better reflect the relevant human components of the tumor microenvironment. However, it usually takes 4-8 months to develop a PDX model, which is longer than the expected survival of many gastric patients. For this reason, establishing primary cancer cell lines may be an effective complementary method for drug response studies. The current protocol describes methods to establish PDX models and primary cancer cell lines from surgical gastric cancer samples. These methods provide a useful tool for drug development and cancer biology research.

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