Rapid validation of cancer genes in chimeras derived from established genetically engineered mouse models

被引:28
作者
Huijbers, Ivo J. [1 ,2 ]
Krimpenfort, Paul [1 ,2 ]
Berns, Anton [1 ,2 ,3 ]
Jonkers, Jos [4 ]
机构
[1] Netherlands Canc Inst, Div Mol Genet, NL-1066 CX Amsterdam, Netherlands
[2] Ctr Biomed Genet, Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[4] Netherlands Canc Inst, Div Mol Biol, NL-1066 CX Amsterdam, Netherlands
关键词
cancer; chimeras; embryonic stem cell; genetically engineered mouse model; non-germline models; recombinase mediated cassette exchange; EMBRYONIC STEM-CELLS; PANCREATIC DUCTAL ADENOCARCINOMA; SOMATIC INACTIVATION; RAT BLASTOCYSTS; K-RAS; MICE; P53; DIFFERENTIATION; PLURIPOTENCY; ACTIVATION;
D O I
10.1002/bies.201100018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent technological advances have opened the door for the fast and cost-effective generation of genetically engineered mouse models (GEMMs) to study cancer. We describe here a conceptually novel approach for the generation of chimeric GEMMs based on the controlled introduction of various genetic elements in embryonic stem cells (ESCs) that are derived from existing mouse strains with a predisposition for cancer. The isolation of GEMM-derived ESC lines is greatly facilitated by the availability of the newly defined culture media containing inhibitors that effectively preserve ESC pluripotency. The feasibility of the GEMM-ESC approach is discussed in light of current literature and placed into the context of existing models. This approach will allow for fast and flexible validation of candidate cancer genes and drug targets and will result in a repository of GEMM-ESC lines and corresponding vector collections that enable easy distribution and use of preclinical models to the wider scientific community.
引用
收藏
页码:701 / 710
页数:10
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