Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/44207
Title: Transposon mouse models to elucidate the genetic mechanisms of hepatitis B viral induced hepatocellular carcinoma
Authors: Chiu, AP
Tschida, BR
Lo, LH
Moriarity, BS
Rowlands, DK
Largaespada, DA
Keng, VW 
Keywords: Forward and reverse genetic screens
Hepatitis B virus
Hepatocellular carcinoma
Sleeping beauty
Transposable elements
Issue Date: 2015
Publisher: WJG Press
Source: World journal of gastroenterology, 2015, v. 21, no. 42, p. 12157-12170 How to cite?
Journal: World journal of gastroenterology 
Abstract: The major type of human liver cancer is hepatocellular carcinoma (HCC), and there are currently many risk factors that contribute to this deadly disease. The majority of HCC occurrences are associated with chronic hepatitis viral infection, and hepatitis B viral (HBV) infection is currently a major health problem in Eastern Asia. Elucidating the genetic mechanisms associated with HBV-induced HCC has been difficult due to the heterogeneity and genetic complexity associated with this disease. A repertoire of animal models has been broadly used to study the pathophysiology and to develop potential treatment regimens for HBVassociated HCC. The use of these animal models has provided valuable genetic information and has been an important contributor to uncovering the factors involved in liver malignant transformation, invasion and metastasis. Recently, transposon-based mouse models are becoming more widely used in liver cancer research to interrogate the genome by forward genetics and also used to validate genes rapidly in a reverse genetic manner. Importantly, these transposon-based rapid reverse genetic mouse models could become crucial in testing potential therapeutic agents before proceeding to clinical trials in human. Therefore, this review will cover the use of transposon-based mouse models to address the problems of liver cancer, especially HBVassociated HCC occurrences in Asia.
URI: http://hdl.handle.net/10397/44207
ISSN: 1007-9327
EISSN: 2219-2840
DOI: 10.3748/wjg.v21.i42.12157
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