Mouse models for liver cancer

被引:126
|
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
相关论文
共 50 条
  • [1] Genetically Engineered Mouse Models for Liver Cancer
    Cho, Kyungjoo
    Ro, Simon Weonsang
    Seo, Sang Hyun
    Jeon, Youjin
    Moon, Hyuk
    Kim, Do Young
    Kim, Seung Up
    CANCERS, 2020, 12 (01)
  • [2] Mouse models of colorectal cancer and liver metastases
    Heijstek, MW
    Kranenburg, O
    Rinkes, IHMB
    DIGESTIVE SURGERY, 2005, 22 (1-2) : 16 - 25
  • [3] Mouse models of liver cancer: Progress and recommendations
    He, Li
    Tian, De-An
    Li, Pei-Yuan
    He, Xing-Xing
    ONCOTARGET, 2015, 6 (27) : 23306 - 23322
  • [4] Genomic Perspective on Mouse Liver Cancer Models
    Yim, Sun Young
    Lee, Ju-Seog
    CANCERS, 2019, 11 (11)
  • [5] Mouse models of spontaneous liver and lung metastasis for colorectal cancer
    Luecke, Joeran
    Mercanoglu, Baris
    Zhang, Tao
    Zazara, Dimitra E.
    Zigmond, Ehud
    Seeger, Philipp
    Mann, Oliver
    Izbicki, Jakob R.
    Hackert, Thilo
    Huber, Samuel
    Giannou, Anastasios D.
    STAR PROTOCOLS, 2024, 5 (01):
  • [6] Molecular mechanisms of hepatocarcinogenesis in transgenic mouse models of liver cancer
    Calvisi, DF
    Thorgeirsson, SS
    TOXICOLOGIC PATHOLOGY, 2005, 33 (01) : 181 - 184
  • [7] Mouse models in liver cancer research:A review of current literature
    Martijn WH Leenders
    Maarten W Nijkamp
    Inne HM Borel Rinkes
    World Journal of Gastroenterology, 2008, 14 (45) : 6915 - 6923
  • [8] MOUSE MODELS FOR HUMAN LIVER CANCER STEM CELL SYNDROME
    Yao, Zhixing
    Li, Ying
    Jogunoori, Wilma S.
    Cao, Hong
    Yao, Wenguo
    Mishra, Bibhuti
    Mishra, Lopa
    HEPATOLOGY, 2009, 50 (04) : 1133A - 1133A
  • [9] Mouse models in liver cancer research: A review of current literature
    Leenders, Martijn W. H.
    Nijkamp, Maarten W.
    Rinkes, Inne H. M. Borel
    WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (45) : 6915 - 6923
  • [10] PDXliver: a database of liver cancer patient derived xenograft mouse models
    He, Sheng
    Hu, Bo
    Li, Chao
    Lin, Ping
    Tang, Wei-Guo
    Sun, Yun-Fan
    Feng, Fang-You-Min
    Guo, Wei
    Li, Jia
    Xu, Yang
    Yao, Qian-Lan
    Zhang, Xin
    Qiu, Shuang-Jian
    Zhou, Jian
    Fan, Jia
    Li, Yi-Xue
    Li, Hong
    Yang, Xin-Rong
    BMC CANCER, 2018, 18