Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in Mice

Epithelial cells in the biliary system can develop refractory types of cancers, which are often associated with inflammation caused by viruses, parasites, stones, and chemicals. Genomic studies have revealed recurrent genetic changes and deregulated signaling pathways in biliary tract cancer (BTC)....

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Main Authors: Masashi Izumiya, Shingo Kato, Yoshitaka Hippo
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/10/2292
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spelling doaj-730e70c172b44729b5c0d61bfc6881a22021-05-31T23:41:46ZengMDPI AGCancers2072-66942021-05-01132292229210.3390/cancers13102292Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in MiceMasashi Izumiya0Shingo Kato1Yoshitaka Hippo2Department of Gastroenterology, The University of Tokyo Hospital, Tokyo 113-8655, JapanDepartment of Clinical Cancer Genomics, Yokohama City University Hospital, Kanagawa 236-0004, JapanDepartment of Molecular Carcinogenesis, Chiba Cancer Center Research Institute, Chiba 260-8717, JapanEpithelial cells in the biliary system can develop refractory types of cancers, which are often associated with inflammation caused by viruses, parasites, stones, and chemicals. Genomic studies have revealed recurrent genetic changes and deregulated signaling pathways in biliary tract cancer (BTC). The causal roles have been at least partly clarified using various genetically engineered mice. Technical advances in Cre-LoxP technology, together with hydrodynamic tail injection, CRISPR/Cas9 technology, in vivo electroporation, and organoid culture have enabled more precise modeling of BTC. Organoid-based genetic modeling, combined with implantation in mice, has recently drawn attention as a means to accelerate the development of BTC models. Although each model may not perfectly mimic the disease, they can complement one another, or two different approaches can be integrated to establish a novel model. In addition, a comparison of the outcomes among these models with the same genotype provides mechanistic insights into the interplay between genetic alterations and the microenvironment in the pathogenesis of BTCs. Here, we review the current status of genetic models of BTCs in mice to provide information that facilitates the wise selection of models and to inform the future development of ideal disease models.https://www.mdpi.com/2072-6694/13/10/2292genetically engineered mousebiliary tract cancerorganoidorthotopic modelnude mousesyngeneic
collection DOAJ
language English
format Article
sources DOAJ
author Masashi Izumiya
Shingo Kato
Yoshitaka Hippo
spellingShingle Masashi Izumiya
Shingo Kato
Yoshitaka Hippo
Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in Mice
Cancers
genetically engineered mouse
biliary tract cancer
organoid
orthotopic model
nude mouse
syngeneic
author_facet Masashi Izumiya
Shingo Kato
Yoshitaka Hippo
author_sort Masashi Izumiya
title Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in Mice
title_short Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in Mice
title_full Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in Mice
title_fullStr Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in Mice
title_full_unstemmed Recent Advances in Implantation-Based Genetic Modeling of Biliary Carcinogenesis in Mice
title_sort recent advances in implantation-based genetic modeling of biliary carcinogenesis in mice
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2021-05-01
description Epithelial cells in the biliary system can develop refractory types of cancers, which are often associated with inflammation caused by viruses, parasites, stones, and chemicals. Genomic studies have revealed recurrent genetic changes and deregulated signaling pathways in biliary tract cancer (BTC). The causal roles have been at least partly clarified using various genetically engineered mice. Technical advances in Cre-LoxP technology, together with hydrodynamic tail injection, CRISPR/Cas9 technology, in vivo electroporation, and organoid culture have enabled more precise modeling of BTC. Organoid-based genetic modeling, combined with implantation in mice, has recently drawn attention as a means to accelerate the development of BTC models. Although each model may not perfectly mimic the disease, they can complement one another, or two different approaches can be integrated to establish a novel model. In addition, a comparison of the outcomes among these models with the same genotype provides mechanistic insights into the interplay between genetic alterations and the microenvironment in the pathogenesis of BTCs. Here, we review the current status of genetic models of BTCs in mice to provide information that facilitates the wise selection of models and to inform the future development of ideal disease models.
topic genetically engineered mouse
biliary tract cancer
organoid
orthotopic model
nude mouse
syngeneic
url https://www.mdpi.com/2072-6694/13/10/2292
work_keys_str_mv AT masashiizumiya recentadvancesinimplantationbasedgeneticmodelingofbiliarycarcinogenesisinmice
AT shingokato recentadvancesinimplantationbasedgeneticmodelingofbiliarycarcinogenesisinmice
AT yoshitakahippo recentadvancesinimplantationbasedgeneticmodelingofbiliarycarcinogenesisinmice
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