医学
肝癌
癌症
癌症研究
生物信息学
计算生物学
内科学
生物
作者
Li He,Dean Tian,Peiyuan Li,Xingxing He
出处
期刊:Oncotarget
[Impact Journals LLC]
日期:2015-06-05
卷期号:6 (27): 23306-23322
被引量:129
标识
DOI:10.18632/oncotarget.4202
摘要
To clarify the pathogenesis of hepatocellular carcinoma (HCC) and investigate the effects of potential therapies, a number of mouse models have been developed. Subcutaneous xenograft models are widely used in the past decades. Yet, with the advent of in vivo imaging technology, investigators are more and more concerned with the orthotopic models nowadays. Genetically engineered mouse models (GEM) have greatly facilitated studies of gene function in HCC development. Recently, GEM of miR-122 and miR-221 provided new approaches for better understanding of the in vivo functions of microRNA in hepatocarcinogenesis. Chemically induced liver tumors in animals share many of the morphological, histogenic, and biochemical features of human HCC. Yet, the complicated and obscure genomic alternation restricts their applications. In this review, we highlight both the frequently used mouse models and some emerging ones with emphasis on their merits or defects, and give advises for investigators to chose a "best-fit" animal model in HCC research.
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