Mouse models for liver cancer

被引:128
作者
Bakiri, Latifa [1 ]
Wagner, Erwin F. [1 ]
机构
[1] Spanish Natl Canc Res Ctr, F BBVA Canc Cell Biol Programme, Genes Dev & Dis Grp, Madrid 28029, Spain
关键词
Liver cancer; Mouse models; Hepatocellular carcinoma models; NF-KAPPA-B; COMPARATIVE FUNCTIONAL GENOMICS; ACTIVATED RECEPTOR-GAMMA; P-GLYCOPROTEIN GENE; HEPATOCELLULAR-CARCINOMA; C-JUN; PEROXISOME-PROLIFERATOR; BETA-CATENIN; COMPENSATORY PROLIFERATION; MOLECULAR PATHOGENESIS;
D O I
10.1016/j.molonc.2013.01.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC), the most common form of primary liver cancer is the third leading cause of cancer-related cell death in human and the fifth in women worldwide. The incidence of HCC is increasing despite progress in identifying risk factors, understanding disease etiology and developing anti-viral strategies. Therapeutic options are limited and survival after diagnosis is poor. Therefore, better preventive, diagnostic and therapeutic tools are urgently needed, in particular given the increased contribution from systemic metabolic disease to HCC incidence worldwide. In the last three decades, technological advances have facilitated the generation of genetically engineered mouse models (GEMMs) to mimic the alterations frequently observed in human cancers or to conduct intervention studies and assess the relevance of candidate gene networks in tumor establishment, progression and maintenance. Because these studies allow molecular and cellular manipulations impossible to perform in patients, GEMMs have improved our understanding of this complex disease and represent a source of great potential for mechanism-based therapy development. In this review, we provide an overview of the current state of HCC modeling in the mouse, highlighting successes, current challenges and future opportunities. (c) 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 223
页数:18
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