- Author:
Hye Lim JU
1
;
Simon Weonsang RO
Author Information
- Publication Type:Review
- Keywords: Hepatocellular carcinoma; Liver cancer animal model
- MeSH: Animals*; Carcinoma, Hepatocellular; Gene Expression; Hepatitis; Hepatocytes; Heterografts; Humans; Hydrodynamics; Liver Neoplasms*; Liver*; Mice; Models, Animal*; Models, Theoretical; Oncogenes; Population Characteristics; Research Personnel; Risk Factors; Signal Transduction
- From:Journal of Liver Cancer 2017;17(1):1-14
- CountryRepublic of Korea
- Language:Korean
- Abstract: Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide. HCC develops in various causes – Viral hepatitis infection, toxins, or other liver conditions - by activation of oncogenes and/or inactivation of tumor suppressors. Understanding of signal pathways and protein-protein interactions critical in tumor development may lead to novel treatment strategy. To evaluate the progression of HCC and effects of potential therapies, various animal models have been established. Experimental models of HCC provide valuable tools to investigate the risk factors, new treatment modalities and biologic characteristics. Subcutaneous xenograft models have been widely used in the past. However, with the advancement of in vivo imaging technology, investigators are more concerned with the orthotopic models nowadays. Genetically engineered mouse models have greatly facilitated studies of gene function in HCC development. Lately, a novel approach for stable gene expression in mouse hepatocytes by hydrodynamic injection has been developed. Each model has its own advantages and disadvantages. Therefore, selecting the optimal models based on study objectives is necessary. In this review, we highlight both the frequently used mouse models and some emerging ones with emphasis on their merits or defects, and give advices for investigators to choose a “best-fit” animal model in HCC research.