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Mouse models of liver cancer: Progress and recommendations

To clarify the pathogenesis of hepatocellular carcinoma (HCC) and investigate the effects of potential therapies, a number of mouse models have been developed. Subcutaneous xenograft models are widely used in the past decades. Yet, with the advent of in vivo imaging technology, investigators are mor...

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Detalles Bibliográficos
Autores principales: He, Li, Tian, De-An, Li, Pei-Yuan, He, Xing-Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695120/
https://www.ncbi.nlm.nih.gov/pubmed/26259234
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author He, Li
Tian, De-An
Li, Pei-Yuan
He, Xing-Xing
author_facet He, Li
Tian, De-An
Li, Pei-Yuan
He, Xing-Xing
author_sort He, Li
collection PubMed
description To clarify the pathogenesis of hepatocellular carcinoma (HCC) and investigate the effects of potential therapies, a number of mouse models have been developed. Subcutaneous xenograft models are widely used in the past decades. Yet, with the advent of in vivo imaging technology, investigators are more and more concerned with the orthotopic models nowadays. Genetically engineered mouse models (GEM) have greatly facilitated studies of gene function in HCC development. Recently, GEM of miR-122 and miR-221 provided new approaches for better understanding of the in vivo functions of microRNA in hepatocarcinogenesis. Chemically induced liver tumors in animals share many of the morphological, histogenic, and biochemical features of human HCC. Yet, the complicated and obscure genomic alternation restricts their applications. In this review, we highlight both the frequently used mouse models and some emerging ones with emphasis on their merits or defects, and give advises for investigators to chose a “best-fit” animal model in HCC research.
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spelling pubmed-46951202016-01-26 Mouse models of liver cancer: Progress and recommendations He, Li Tian, De-An Li, Pei-Yuan He, Xing-Xing Oncotarget Review To clarify the pathogenesis of hepatocellular carcinoma (HCC) and investigate the effects of potential therapies, a number of mouse models have been developed. Subcutaneous xenograft models are widely used in the past decades. Yet, with the advent of in vivo imaging technology, investigators are more and more concerned with the orthotopic models nowadays. Genetically engineered mouse models (GEM) have greatly facilitated studies of gene function in HCC development. Recently, GEM of miR-122 and miR-221 provided new approaches for better understanding of the in vivo functions of microRNA in hepatocarcinogenesis. Chemically induced liver tumors in animals share many of the morphological, histogenic, and biochemical features of human HCC. Yet, the complicated and obscure genomic alternation restricts their applications. In this review, we highlight both the frequently used mouse models and some emerging ones with emphasis on their merits or defects, and give advises for investigators to chose a “best-fit” animal model in HCC research. Impact Journals LLC 2015-06-05 /pmc/articles/PMC4695120/ /pubmed/26259234 Text en Copyright: © 2015 He et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
He, Li
Tian, De-An
Li, Pei-Yuan
He, Xing-Xing
Mouse models of liver cancer: Progress and recommendations
title Mouse models of liver cancer: Progress and recommendations
title_full Mouse models of liver cancer: Progress and recommendations
title_fullStr Mouse models of liver cancer: Progress and recommendations
title_full_unstemmed Mouse models of liver cancer: Progress and recommendations
title_short Mouse models of liver cancer: Progress and recommendations
title_sort mouse models of liver cancer: progress and recommendations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695120/
https://www.ncbi.nlm.nih.gov/pubmed/26259234
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