Genomic Perspective on Mouse Liver Cancer Models

被引:10
|
作者
Yim, Sun Young [1 ]
Lee, Ju-Seog [2 ]
机构
[1] Korea Univ, Dept Internal Med, Div Gastroenterol & Hepatol, Coll Med, Seoul 136701, South Korea
[2] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Dept Canc Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
mouse model; hepatocellular carcinoma; ctnnb1; arid1a; sv40; genomics; hippo pathway; genomic resemblance; WNT/BETA-CATENIN PATHWAY; GROWTH-FACTOR-ALPHA; HEPATOCELLULAR-CARCINOMA; C-MYC; TRANSGENIC MICE; BETA-CATENIN; MUTATIONAL LANDSCAPE; SOMATIC MUTATIONS; HIPPO PATHWAY; T-ANTIGEN;
D O I
10.3390/cancers11111648
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Selecting the most appropriate mouse model that best recapitulates human hepatocellular carcinoma (HCC) allows translation of preclinical mouse studies into clinical studies. In the era of cancer genomics, comprehensive and integrative analysis of the human HCC genome has allowed categorization of HCC according to molecular subtypes. Despite the variety of mouse models that are available for preclinical research, there is a lack of evidence for mouse models that closely resemble human HCC. Therefore, it is necessary to identify the accurate mouse models that represent human HCC based on molecular subtype as well as histologic aggressiveness. In this review, we summarize the mouse models integrated with human HCC genomic data to provide information regarding the models that recapitulates the distinct aspect of HCC biology and prognosis based on molecular subtypes.
引用
收藏
页数:14
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