Genetically engineered mouse models for hereditary cancer syndromes

被引:1
|
作者
Biswas, Kajal [1 ]
Mohammed, Altaf
Sharan, Shyam K. [2 ]
Shoemaker, Robert H. [1 ,3 ]
机构
[1] NCI, Div Canc Prevent, Chemoprevent Agent Dev Res Grp, Rockville, MD USA
[2] NCI, NIH, Ctr Canc Res, Mouse Canc Genet Program, Frederick, MD USA
[3] 9609 Med Ctr Dr, Room 5E454, Rockville, MD 20850 USA
关键词
cancer genetics; disease model; genetically engineered mice; hereditary cancers; mouse models; DNA MISMATCH REPAIR; TUMOR SUSCEPTIBILITY; EMBRYONIC LETHALITY; DEFICIENCY SYNDROME; MICE DEFICIENT; OVARIAN-CANCER; MUTATION; BRCA1; BREAST; MSH6;
D O I
10.1111/cas.15737
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Advances in molecular diagnostics have led to improved diagnosis and molecular understanding of hereditary cancers in the clinic. Improving the management, treatment, and potential prevention of cancers in carriers of predisposing mutations requires preclinical experimental models that reflect the key pathogenic features of the specific syndrome associated with the mutations. Numerous genetically engineered mouse (GEM) models of hereditary cancer have been developed. In this review, we describe the models of Lynch syndrome and hereditary breast and ovarian cancer syndrome, the two most common hereditary cancer predisposition syndromes. We focus on Lynch syndrome models as illustrative of the potential for using mouse models to devise improved approaches to prevention of cancer in a high-risk population. GEM models are an invaluable tool for hereditary cancer models. Here, we review GEM models for some hereditary cancers and their potential use in cancer prevention studies.
引用
收藏
页码:1800 / 1815
页数:16
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