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

被引:6
作者
Lu, Jia-huan [1 ]
Wang, Yun [1 ]
Meng, Qi [1 ]
Zeng, Zhao-lei [1 ]
机构
[1] Sun Yat Sen Univ, Canc Ctr, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangzhou, Guangdong, Peoples R China
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2019年 / 149期
基金
中国国家自然科学基金;
关键词
Cancer Research; Issue; 149; primary tumor cell line; patient-derived xenograft; gastric cancer; heterogeneity; therapeutic strategy; tissue cryopreservation; ENGRAFTMENT; MOUSE; ERA;
D O I
10.3791/59871
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
收藏
页数:6
相关论文
共 21 条
[1]   Maintaining Tumor Heterogeneity in Patient-Derived Tumor Xenografts [J].
Cassidy, John W. ;
Caldas, Carlos ;
Bruna, Alejandra .
CANCER RESEARCH, 2015, 75 (15) :2963-2968
[2]   Evolution of Gastric Cancer Treatment: From the Golden Age of Surgery to an Era of Precision Medicine [J].
Choi, Yoon Young ;
Noh, Sung Hoon ;
Cheong, Jae-Ho .
YONSEI MEDICAL JOURNAL, 2015, 56 (05) :1177-1185
[3]   Advanced gastric cancer: what we know and what we still have to learn [J].
Coccolini, Federico ;
Montori, Giulia ;
Ceresoli, Marco ;
Cima, Simona ;
Valli, Maria Carla ;
Nita, Gabriela E. ;
Heyer, Arianna ;
Catena, Fausto ;
Ansaloni, Luca .
WORLD JOURNAL OF GASTROENTEROLOGY, 2016, 22 (03) :1139-1159
[4]   Multimodal treatment in locally advanced gastric cancer [J].
Goetze, Oliver Thorsten ;
Al-Batran, Salah-Eddin ;
Chevallay, Mickael ;
Moenig, Stefan Paul .
UPDATES IN SURGERY, 2018, 70 (02) :173-179
[5]   Multimodal Treatment of Locally Advanced Gastric Cancer: Will the West Meet the East? [J].
Graziosi, Luigina ;
Marino, Elisabetta ;
Donini, Annibale .
ANNALS OF SURGICAL ONCOLOGY, 2019, 26 (03) :918-918
[6]   NOD/SCID/γcnull mouse:: an excellent recipient mouse model for engraftment of human cells [J].
Ito, M ;
Hiramatsu, H ;
Kobayashi, K ;
Suzue, K ;
Kawahata, M ;
Hioki, K ;
Ueyama, Y ;
Koyanagi, Y ;
Sugamura, K ;
Tsuji, K ;
Heike, T ;
Nakahata, T .
BLOOD, 2002, 100 (09) :3175-3182
[7]  
Jemal A, 2011, CA-CANCER J CLIN, V61, P134, DOI [10.3322/caac.21492, 10.3322/caac.20115, 10.3322/caac.20107]
[8]   Current Update of Patient-Derived Xenograft Model for Translational Breast Cancer Research [J].
Kawaguchi, Tsutomu ;
Foster, Barbara A. ;
Young, Jessica ;
Takabe, Kazuaki .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 2017, 22 (02) :131-139
[9]   Current status and perspectives of patient-derived xenograft models in cancer research [J].
Lai, Yunxin ;
Wei, Xinru ;
Lin, Shouheng ;
Qin, Le ;
Cheng, Lin ;
Li, Peng .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2017, 10
[10]   Gastric Cancer in the Era of Precision Medicine [J].
Liu, Xi ;
Meltzer, Stephen J. .
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2017, 3 (03) :348-358