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Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models
The study of pancreatic cancer has prompted the development of numerous mouse models that aim to recapitulate the phenotypic and mechanistic features of this deadly malignancy. This review accomplishes two tasks. First, it provides an overview of the models that have been used as representations of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255505/ https://www.ncbi.nlm.nih.gov/pubmed/25538623 http://dx.doi.org/10.3389/fphys.2014.00464 |
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author | DeCant, Brian T. Principe, Daniel R. Guerra, Carmen Pasca di Magliano, Marina Grippo, Paul J. |
author_facet | DeCant, Brian T. Principe, Daniel R. Guerra, Carmen Pasca di Magliano, Marina Grippo, Paul J. |
author_sort | DeCant, Brian T. |
collection | PubMed |
description | The study of pancreatic cancer has prompted the development of numerous mouse models that aim to recapitulate the phenotypic and mechanistic features of this deadly malignancy. This review accomplishes two tasks. First, it provides an overview of the models that have been used as representations of both the neoplastic and carcinoma phenotypes. Second, it presents new modeling schemes that ultimately will serve to more faithfully capture the temporal and spatial progression of the human disease, providing platforms for improved understanding of the role of non-epithelial compartments in disease etiology as well as evaluating therapeutic approaches. |
format | Online Article Text |
id | pubmed-4255505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42555052014-12-23 Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models DeCant, Brian T. Principe, Daniel R. Guerra, Carmen Pasca di Magliano, Marina Grippo, Paul J. Front Physiol Physiology The study of pancreatic cancer has prompted the development of numerous mouse models that aim to recapitulate the phenotypic and mechanistic features of this deadly malignancy. This review accomplishes two tasks. First, it provides an overview of the models that have been used as representations of both the neoplastic and carcinoma phenotypes. Second, it presents new modeling schemes that ultimately will serve to more faithfully capture the temporal and spatial progression of the human disease, providing platforms for improved understanding of the role of non-epithelial compartments in disease etiology as well as evaluating therapeutic approaches. Frontiers Media S.A. 2014-12-04 /pmc/articles/PMC4255505/ /pubmed/25538623 http://dx.doi.org/10.3389/fphys.2014.00464 Text en Copyright © 2014 DeCant, Prinicipe, Guerra, Pasca di Magliano and Grippo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology DeCant, Brian T. Principe, Daniel R. Guerra, Carmen Pasca di Magliano, Marina Grippo, Paul J. Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models |
title | Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models |
title_full | Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models |
title_fullStr | Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models |
title_full_unstemmed | Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models |
title_short | Utilizing past and present mouse systems to engineer more relevant pancreatic cancer models |
title_sort | utilizing past and present mouse systems to engineer more relevant pancreatic cancer models |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255505/ https://www.ncbi.nlm.nih.gov/pubmed/25538623 http://dx.doi.org/10.3389/fphys.2014.00464 |
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