Mouse models for the discovery of colorectal cancer driver genes

被引:9
|
作者
Clark, Christopher R. [1 ]
Starr, Timothy K. [1 ]
机构
[1] Univ Minnesota, Dept Obstet Gynecol & Womens Hlth, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
Mouse models; Colorectal cancer; Cancer genes; Insertional mutagenesis; Transposable elements; MULTIPLE INTESTINAL NEOPLASIA; MISMATCH REPAIR GENES; SLEEPING-BEAUTY; MICROSATELLITE INSTABILITY; INSERTIONAL MUTAGENESIS; GERMLINE MUTATIONS; PROGNOSTIC IMPACT; IDENTIFIES GENES; MUTL HOMOLOG; HUMAN BREAST;
D O I
10.3748/wjg.v22.i2.815
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Colorectal cancer (CRC) constitutes a major public health problem as the third most commonly diagnosed and third most lethal malignancy worldwide. The prevalence and the physical accessibility to colorectal tumors have made CRC an ideal model for the study of tumor genetics. Early research efforts using patient derived CRC samples led to the discovery of several highly penetrant mutations (e.g., APC, KRAS, MMR genes) in both hereditary and sporadic CRC tumors. This knowledge has enabled researchers to develop genetically engineered and chemically induced tumor models of CRC, both of which have had a substantial impact on our understanding of the molecular basis of CRC. Despite these advances, the morbidity and mortality of CRC remains a cause for concern and highlight the need to uncover novel genetic drivers of CRC. This review focuses on mouse models of CRC with particular emphasis on a newly developed cancer gene discovery tool, the Sleeping Beauty transposon- based mutagenesis model of CRC.
引用
收藏
页码:815 / 822
页数:8
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