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TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis
Truncating mutations in the tumor suppressor gene adenomatous polyposis coli (APC) are the initiating step in the vast majority of sporadic colorectal cancers, and they underlie familial adenomatous polyposis (FAP) syndromes. Modeling of APC- driven tumor formation in the mouse has contributed subst...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468341/ https://www.ncbi.nlm.nih.gov/pubmed/26097888 |
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author | Van Nieuwenhuysen, Tom Naert, Thomas Tran, Hong Thi Van Imschoot, Griet Geurs, Sarah Sanders, Ellen Creytens, David Van Roy, Frans Vleminckx, Kris |
author_facet | Van Nieuwenhuysen, Tom Naert, Thomas Tran, Hong Thi Van Imschoot, Griet Geurs, Sarah Sanders, Ellen Creytens, David Van Roy, Frans Vleminckx, Kris |
author_sort | Van Nieuwenhuysen, Tom |
collection | PubMed |
description | Truncating mutations in the tumor suppressor gene adenomatous polyposis coli (APC) are the initiating step in the vast majority of sporadic colorectal cancers, and they underlie familial adenomatous polyposis (FAP) syndromes. Modeling of APC- driven tumor formation in the mouse has contributed substantially to our mechanistic understanding of the associated disease, but additional models are needed to explore therapeutic opportunities and overcome current limitations of mouse models. We report on a novel and penetrant genetic cancer model in Xenopus tropicalis, an aquatic tetrapod vertebrate with external development, diploid genome and short life cycle. Tadpoles and froglets derived from embryos injected with TAL effector nucleases targeting the apc gene rapidly developed intestinal hyperplasia and other neoplasms observed in FAP patients, including desmoid tumors and medulloblastomas. Bi-allelic apc mutations causing frame shifts were detected in the tumors, which displayed activation of the Wnt/β-catenin pathway and showed increased cellular proliferation. We further demonstrate that simultaneous double bi-allelic mutation of apc and a non-relevant gene is possible in the neoplasias, opening the door for identification and characterization of effector or modifier genes in tumors expressing truncated apc. Our results demonstrate the power of modeling human cancer in Xenopus tropicalis using mosaic TALEN-mediated bi-allelic gene disruption. |
format | Online Article Text |
id | pubmed-4468341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-44683412015-06-19 TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis Van Nieuwenhuysen, Tom Naert, Thomas Tran, Hong Thi Van Imschoot, Griet Geurs, Sarah Sanders, Ellen Creytens, David Van Roy, Frans Vleminckx, Kris Oncoscience Research Paper Truncating mutations in the tumor suppressor gene adenomatous polyposis coli (APC) are the initiating step in the vast majority of sporadic colorectal cancers, and they underlie familial adenomatous polyposis (FAP) syndromes. Modeling of APC- driven tumor formation in the mouse has contributed substantially to our mechanistic understanding of the associated disease, but additional models are needed to explore therapeutic opportunities and overcome current limitations of mouse models. We report on a novel and penetrant genetic cancer model in Xenopus tropicalis, an aquatic tetrapod vertebrate with external development, diploid genome and short life cycle. Tadpoles and froglets derived from embryos injected with TAL effector nucleases targeting the apc gene rapidly developed intestinal hyperplasia and other neoplasms observed in FAP patients, including desmoid tumors and medulloblastomas. Bi-allelic apc mutations causing frame shifts were detected in the tumors, which displayed activation of the Wnt/β-catenin pathway and showed increased cellular proliferation. We further demonstrate that simultaneous double bi-allelic mutation of apc and a non-relevant gene is possible in the neoplasias, opening the door for identification and characterization of effector or modifier genes in tumors expressing truncated apc. Our results demonstrate the power of modeling human cancer in Xenopus tropicalis using mosaic TALEN-mediated bi-allelic gene disruption. Impact Journals LLC 2015-05-19 /pmc/articles/PMC4468341/ /pubmed/26097888 Text en © 2015 Van Nieuwenhuysen 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 | Research Paper Van Nieuwenhuysen, Tom Naert, Thomas Tran, Hong Thi Van Imschoot, Griet Geurs, Sarah Sanders, Ellen Creytens, David Van Roy, Frans Vleminckx, Kris TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis |
title | TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis |
title_full | TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis |
title_fullStr | TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis |
title_full_unstemmed | TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis |
title_short | TALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis |
title_sort | talen-mediated apc mutation in xenopus tropicalis phenocopies familial adenomatous polyposis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468341/ https://www.ncbi.nlm.nih.gov/pubmed/26097888 |
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