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Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers

Wildlife populations are under intense anthropogenic pressures, with the geographic range of many species shrinking, dramatic reductions in population numbers and undisturbed habitats, and biodiversity loss. It is postulated that we are in the midst of a sixth (Anthropocene) mass extinction event, t...

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Autores principales: Duffy, David J., Schnitzler, Christine, Karpinski, Lorraine, Thomas, Rachel, Whilde, Jenny, Eastman, Catherine, Yang, Calvin, Krstic, Aleksandar, Rollinson, Devon, Zirkelbach, Bette, Yetsko, Kelsey, Burkhalter, Brooke, Martindale, Mark Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123702/
https://www.ncbi.nlm.nih.gov/pubmed/30271945
http://dx.doi.org/10.1038/s42003-018-0059-x
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author Duffy, David J.
Schnitzler, Christine
Karpinski, Lorraine
Thomas, Rachel
Whilde, Jenny
Eastman, Catherine
Yang, Calvin
Krstic, Aleksandar
Rollinson, Devon
Zirkelbach, Bette
Yetsko, Kelsey
Burkhalter, Brooke
Martindale, Mark Q.
author_facet Duffy, David J.
Schnitzler, Christine
Karpinski, Lorraine
Thomas, Rachel
Whilde, Jenny
Eastman, Catherine
Yang, Calvin
Krstic, Aleksandar
Rollinson, Devon
Zirkelbach, Bette
Yetsko, Kelsey
Burkhalter, Brooke
Martindale, Mark Q.
author_sort Duffy, David J.
collection PubMed
description Wildlife populations are under intense anthropogenic pressures, with the geographic range of many species shrinking, dramatic reductions in population numbers and undisturbed habitats, and biodiversity loss. It is postulated that we are in the midst of a sixth (Anthropocene) mass extinction event, the first to be induced by human activity. Further, threatening vulnerable species is the increased rate of emerging diseases, another consequence of anthropogenic activities. Innovative approaches are required to help maintain healthy populations until the chronic underlying causes of these issues can be addressed. Fibropapillomatosis in sea turtles is one such wildlife disease. Here, we applied precision-medicine-based approaches to profile fibropapillomatosis tumors to better understand their biology, identify novel therapeutics, and gain insights into viral and environmental triggers for fibropapillomatosis. We show that fibropapillomatosis tumors share genetic vulnerabilities with human cancer types, revealing that they are amenable to treatment with human anti-cancer therapeutics.
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spelling pubmed-61237022018-09-28 Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers Duffy, David J. Schnitzler, Christine Karpinski, Lorraine Thomas, Rachel Whilde, Jenny Eastman, Catherine Yang, Calvin Krstic, Aleksandar Rollinson, Devon Zirkelbach, Bette Yetsko, Kelsey Burkhalter, Brooke Martindale, Mark Q. Commun Biol Article Wildlife populations are under intense anthropogenic pressures, with the geographic range of many species shrinking, dramatic reductions in population numbers and undisturbed habitats, and biodiversity loss. It is postulated that we are in the midst of a sixth (Anthropocene) mass extinction event, the first to be induced by human activity. Further, threatening vulnerable species is the increased rate of emerging diseases, another consequence of anthropogenic activities. Innovative approaches are required to help maintain healthy populations until the chronic underlying causes of these issues can be addressed. Fibropapillomatosis in sea turtles is one such wildlife disease. Here, we applied precision-medicine-based approaches to profile fibropapillomatosis tumors to better understand their biology, identify novel therapeutics, and gain insights into viral and environmental triggers for fibropapillomatosis. We show that fibropapillomatosis tumors share genetic vulnerabilities with human cancer types, revealing that they are amenable to treatment with human anti-cancer therapeutics. Nature Publishing Group UK 2018-06-07 /pmc/articles/PMC6123702/ /pubmed/30271945 http://dx.doi.org/10.1038/s42003-018-0059-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Duffy, David J.
Schnitzler, Christine
Karpinski, Lorraine
Thomas, Rachel
Whilde, Jenny
Eastman, Catherine
Yang, Calvin
Krstic, Aleksandar
Rollinson, Devon
Zirkelbach, Bette
Yetsko, Kelsey
Burkhalter, Brooke
Martindale, Mark Q.
Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers
title Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers
title_full Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers
title_fullStr Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers
title_full_unstemmed Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers
title_short Sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers
title_sort sea turtle fibropapilloma tumors share genomic drivers and therapeutic vulnerabilities with human cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123702/
https://www.ncbi.nlm.nih.gov/pubmed/30271945
http://dx.doi.org/10.1038/s42003-018-0059-x
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