TY - JOUR
T1 - Transposon mouse models to elucidate the genetic mechanisms of hepatitis B viral induced hepatocellular carcinoma
AU - Chiu, Amy P.
AU - Tschida, Barbara R.
AU - Lo, Lilian H.
AU - Moriarity, Branden S.
AU - Rowlands, Dewi K.
AU - Largaespada, David A.
AU - Keng, Wee-Keong Vincent
PY - 2015/11/14
Y1 - 2015/11/14
N2 - 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.
AB - 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.
KW - Forward and reverse genetic screens
KW - Hepatitis B virus
KW - Hepatocellular carcinoma
KW - Sleeping Beauty
KW - Transposable elements
UR - http://www.scopus.com/inward/record.url?scp=84947460425&partnerID=8YFLogxK
U2 - 10.3748/wjg.v21.i42.12157
DO - 10.3748/wjg.v21.i42.12157
M3 - Review article
C2 - 26576100
SN - 1007-9327
VL - 21
SP - 12157
EP - 12170
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 42
ER -