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52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES

Central nervous system (CNS), notably brain, metastases are most prevalent in lung cancer (20–56% of patients), breast cancer (5–20%) and melanoma (7–16%). Lesions occur in both the brain parenchyma and the meninges. To mechanistically understand CNS metastasis formation and develop preventive and t...

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Autores principales: Valiente, Manuel, Van Swearingen, Amanda, Anders, Carey, Bairoch, Amos, Boire, Adrienne, Bos, Paula, Cittelly, Diana, Erez, Neta, Ferrarro, Gino, Fukumura, Dai, Gril, Brunilde, Herlyn, Meenhard, Holmen, Sheri, Jain, Rakesh, Joyce, Johanna, Lorger, Mihaela, Massague, Joan, Neman, Josh, Sibson, Nicola, Steeg, Patricia, Thorsen, Frits, Young, Leonie, Vareslija, Damir, Vultur, Adina, Weis-Garcia, Frances, Winkler, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401335/
http://dx.doi.org/10.1093/noajnl/vdaa073.040
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author Valiente, Manuel
Van Swearingen, Amanda
Anders, Carey
Bairoch, Amos
Boire, Adrienne
Bos, Paula
Cittelly, Diana
Erez, Neta
Ferrarro, Gino
Fukumura, Dai
Gril, Brunilde
Herlyn, Meenhard
Holmen, Sheri
Jain, Rakesh
Joyce, Johanna
Lorger, Mihaela
Massague, Joan
Neman, Josh
Sibson, Nicola
Steeg, Patricia
Thorsen, Frits
Young, Leonie
Vareslija, Damir
Vultur, Adina
Weis-Garcia, Frances
Winkler, Frank
author_facet Valiente, Manuel
Van Swearingen, Amanda
Anders, Carey
Bairoch, Amos
Boire, Adrienne
Bos, Paula
Cittelly, Diana
Erez, Neta
Ferrarro, Gino
Fukumura, Dai
Gril, Brunilde
Herlyn, Meenhard
Holmen, Sheri
Jain, Rakesh
Joyce, Johanna
Lorger, Mihaela
Massague, Joan
Neman, Josh
Sibson, Nicola
Steeg, Patricia
Thorsen, Frits
Young, Leonie
Vareslija, Damir
Vultur, Adina
Weis-Garcia, Frances
Winkler, Frank
author_sort Valiente, Manuel
collection PubMed
description Central nervous system (CNS), notably brain, metastases are most prevalent in lung cancer (20–56% of patients), breast cancer (5–20%) and melanoma (7–16%). Lesions occur in both the brain parenchyma and the meninges. To mechanistically understand CNS metastasis formation and develop preventive and therapeutic strategies, it is essential to use model systems that, as much as possible, faithfully recapitulate the clinical disease process. Furthermore, the complexities of brain metastases dictate that studies should utilize multiple model systems in various stages of brain metastases progression. To facilitate brain metastasis research, 19 laboratories around the world have compiled comprehensive information on their brain metastasis mouse models. Each lab has provided details on the cell lines that they have generated or characterized as being capable of forming metastatic colonies in the brain, as well as principle methodologies of brain metastasis research. This Brain Metastasis Cell Lines Panel (BrMPanel, https://apps.cnio.es/app/BrainMetastasis/CellLines) represents the first of its class and includes information about each cell line, how tropism to the brain was established, and the behavior of each model in vivo. The BrMPanel is composed of 60 cell lines, derived from patients (32 cell lines, 53%), mouse (27, 45%) or rat (1, 2%), and represent the three main cancer types that result in brain metastasis: breast cancer (38 cell lines, 63%), lung cancer (8, 13%) and melanoma (14, 23%). This resource is intended to assist investigators in choosing the most suitable model for research on brain metastasis, and is available to the entire scientific community. The ultimate goal of this effort is to facilitate research on this unmet clinical need, to improve models through a collaborative environment, and to promote the exchange of information on these valuable resources. We invite other collaborators to contribute their models to the BrMPanel to grow this resource.
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spelling pubmed-74013352020-08-06 52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES Valiente, Manuel Van Swearingen, Amanda Anders, Carey Bairoch, Amos Boire, Adrienne Bos, Paula Cittelly, Diana Erez, Neta Ferrarro, Gino Fukumura, Dai Gril, Brunilde Herlyn, Meenhard Holmen, Sheri Jain, Rakesh Joyce, Johanna Lorger, Mihaela Massague, Joan Neman, Josh Sibson, Nicola Steeg, Patricia Thorsen, Frits Young, Leonie Vareslija, Damir Vultur, Adina Weis-Garcia, Frances Winkler, Frank Neurooncol Adv Supplement Abstracts Central nervous system (CNS), notably brain, metastases are most prevalent in lung cancer (20–56% of patients), breast cancer (5–20%) and melanoma (7–16%). Lesions occur in both the brain parenchyma and the meninges. To mechanistically understand CNS metastasis formation and develop preventive and therapeutic strategies, it is essential to use model systems that, as much as possible, faithfully recapitulate the clinical disease process. Furthermore, the complexities of brain metastases dictate that studies should utilize multiple model systems in various stages of brain metastases progression. To facilitate brain metastasis research, 19 laboratories around the world have compiled comprehensive information on their brain metastasis mouse models. Each lab has provided details on the cell lines that they have generated or characterized as being capable of forming metastatic colonies in the brain, as well as principle methodologies of brain metastasis research. This Brain Metastasis Cell Lines Panel (BrMPanel, https://apps.cnio.es/app/BrainMetastasis/CellLines) represents the first of its class and includes information about each cell line, how tropism to the brain was established, and the behavior of each model in vivo. The BrMPanel is composed of 60 cell lines, derived from patients (32 cell lines, 53%), mouse (27, 45%) or rat (1, 2%), and represent the three main cancer types that result in brain metastasis: breast cancer (38 cell lines, 63%), lung cancer (8, 13%) and melanoma (14, 23%). This resource is intended to assist investigators in choosing the most suitable model for research on brain metastasis, and is available to the entire scientific community. The ultimate goal of this effort is to facilitate research on this unmet clinical need, to improve models through a collaborative environment, and to promote the exchange of information on these valuable resources. We invite other collaborators to contribute their models to the BrMPanel to grow this resource. Oxford University Press 2020-08-04 /pmc/articles/PMC7401335/ http://dx.doi.org/10.1093/noajnl/vdaa073.040 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Supplement Abstracts
Valiente, Manuel
Van Swearingen, Amanda
Anders, Carey
Bairoch, Amos
Boire, Adrienne
Bos, Paula
Cittelly, Diana
Erez, Neta
Ferrarro, Gino
Fukumura, Dai
Gril, Brunilde
Herlyn, Meenhard
Holmen, Sheri
Jain, Rakesh
Joyce, Johanna
Lorger, Mihaela
Massague, Joan
Neman, Josh
Sibson, Nicola
Steeg, Patricia
Thorsen, Frits
Young, Leonie
Vareslija, Damir
Vultur, Adina
Weis-Garcia, Frances
Winkler, Frank
52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES
title 52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES
title_full 52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES
title_fullStr 52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES
title_full_unstemmed 52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES
title_short 52. BrMPANEL: A PUBLIC RESOURCE OF ORGANOTROPIC CELL LINES
title_sort 52. brmpanel: a public resource of organotropic cell lines
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401335/
http://dx.doi.org/10.1093/noajnl/vdaa073.040
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