Rational Design of Mouse Models for Cancer Research

被引:57
作者
Landgraf, Marietta [1 ]
McGovern, Jacqui A. [1 ]
Friedl, Peter [2 ,3 ,4 ]
Hutmacher, Dietmar W. [1 ,5 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Ctr Regenerat Med, Brisbane, Qld, Australia
[2] Radboud Univ Nijmegen, Med Ctr, Dept Cell Biol, Post 283,POB 9101, NL-6500 HB Nijmegen, Netherlands
[3] Univ Texas MD Anderson Canc Ctr, Genitourinary Med Oncol Res, Houston, TX 77030 USA
[4] Canc Genom Ctr, Utrecht, Netherlands
[5] Georgia Inst Technol, George W Woodruff Sch Mech Engn, 801 Ferst Dr Northwest, Atlanta, GA 30332 USA
基金
欧洲研究理事会; 英国医学研究理事会;
关键词
SYNTHETIC BIOLOGY; HUMANIZED MICE; SYSTEMS BIOLOGY; BONE ORGAN; PATIENT; CELLS; MEDICINE; XENOGRAFTS; GENERATION; GENES;
D O I
10.1016/j.tibtech.2017.12.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The laboratory mouse is widely considered as a valid and affordable model organism to study human disease. Attempts to improve the relevance of murine models for the investigation of human pathologies led to the development of various genetically engineered, xenograft and humanized mouse models. Nevertheless, most preclinical studies in mice suffer from insufficient predictive value when compared with cancer biology and therapy response of human patients. We propose an innovative strategy to improve the predictive power of preclinical cancer models. Combining (i) genomic, tissue engineering and regenerative medicine approaches for rational design of mouse models with (ii) rapid prototyping and computational benchmarking against human clinical data will enable fast and nonbiased validation of newly generated models.
引用
收藏
页码:242 / 251
页数:10
相关论文
共 60 条
[1]   Preclinical intravital microscopy of the tumour-stroma interface: invasion, metastasis, and therapy response [J].
Alexander, Stephanie ;
Weigelin, Bettina ;
Winkler, Frank ;
Friedl, Peter .
CURRENT OPINION IN CELL BIOLOGY, 2013, 25 (05) :659-671
[2]  
[Anonymous], NAT BIOTECHNOL, V33, P671
[3]   Examining the utility of patient-derived xenograft mouse models [J].
Aparicio, Samuel ;
Hidalgo, Manuel ;
Kung, Andrew L. .
NATURE REVIEWS CANCER, 2015, 15 (05) :311-316
[4]  
Attarwala H, 2010, J Young Pharm, V2, P332, DOI 10.4103/0975-1483.66810
[5]   Periosteum tissue engineering in an orthotopic in vivo platform [J].
Baldwin, J. G. ;
Wagner, F. ;
Martine, L. C. ;
Holzapfel, B. M. ;
Theodoropoulos, C. ;
Bas, O. ;
Savi, F. M. ;
Werner, C. ;
De-Juan-Pardo, E. M. ;
Hutmacher, D. W. .
BIOMATERIALS, 2017, 121 :193-204
[6]   Putting tumours in context [J].
Bissell, MJ ;
Radisky, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :46-54
[7]   Overcoming Current Limitations in Humanized Mouse Research [J].
Brehm, Michael A. ;
Shultz, Leonard D. ;
Luban, Jeremy ;
Greiner, Dale L. .
JOURNAL OF INFECTIOUS DISEASES, 2013, 208 :S125-S130
[8]   Synthetic Biology in the Driving Seat of the Bioeconomy [J].
Bueso, Yensi Flores ;
Tangney, Mark .
TRENDS IN BIOTECHNOLOGY, 2017, 35 (05) :373-378
[9]   Synthetic biology in cell-based cancer immunotherapy [J].
Chakravarti, Deboki ;
Wong, Wilson W. .
TRENDS IN BIOTECHNOLOGY, 2015, 33 (08) :449-461
[10]  
Cho Andrew, 2009, Curr Protoc Cell Biol, VChapter 19, DOI 10.1002/0471143030.cb1911s42