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Cross‐species models of human melanoma
Although transformation of melanocytes to melanoma is rare, the rapid growth, systemic spread, as well as the chemoresistance of melanoma present significant challenges for patient care. Here we review animal models of melanoma, including murine, canine, equine, and zebrafish models, and detail the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832391/ https://www.ncbi.nlm.nih.gov/pubmed/26354726 http://dx.doi.org/10.1002/path.4632 |
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author | van der Weyden, Louise Patton, E Elizabeth Wood, Geoffrey A Foote, Alastair K Brenn, Thomas Arends, Mark J Adams, David J |
author_facet | van der Weyden, Louise Patton, E Elizabeth Wood, Geoffrey A Foote, Alastair K Brenn, Thomas Arends, Mark J Adams, David J |
author_sort | van der Weyden, Louise |
collection | PubMed |
description | Although transformation of melanocytes to melanoma is rare, the rapid growth, systemic spread, as well as the chemoresistance of melanoma present significant challenges for patient care. Here we review animal models of melanoma, including murine, canine, equine, and zebrafish models, and detail the immense contribution these models have made to our knowledge of human melanoma development, and to melanocyte biology. We also highlight the opportunities for cross‐species comparative genomic studies of melanoma to identify the key molecular events that drive this complex disease. © 2015 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. |
format | Online Article Text |
id | pubmed-4832391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48323912016-04-20 Cross‐species models of human melanoma van der Weyden, Louise Patton, E Elizabeth Wood, Geoffrey A Foote, Alastair K Brenn, Thomas Arends, Mark J Adams, David J J Pathol Invited Reviews Although transformation of melanocytes to melanoma is rare, the rapid growth, systemic spread, as well as the chemoresistance of melanoma present significant challenges for patient care. Here we review animal models of melanoma, including murine, canine, equine, and zebrafish models, and detail the immense contribution these models have made to our knowledge of human melanoma development, and to melanocyte biology. We also highlight the opportunities for cross‐species comparative genomic studies of melanoma to identify the key molecular events that drive this complex disease. © 2015 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. John Wiley & Sons, Ltd 2015-10-09 2016-01 /pmc/articles/PMC4832391/ /pubmed/26354726 http://dx.doi.org/10.1002/path.4632 Text en © 2015 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Reviews van der Weyden, Louise Patton, E Elizabeth Wood, Geoffrey A Foote, Alastair K Brenn, Thomas Arends, Mark J Adams, David J Cross‐species models of human melanoma |
title | Cross‐species models of human melanoma |
title_full | Cross‐species models of human melanoma |
title_fullStr | Cross‐species models of human melanoma |
title_full_unstemmed | Cross‐species models of human melanoma |
title_short | Cross‐species models of human melanoma |
title_sort | cross‐species models of human melanoma |
topic | Invited Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832391/ https://www.ncbi.nlm.nih.gov/pubmed/26354726 http://dx.doi.org/10.1002/path.4632 |
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