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Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish

Cancers contain a wide diversity of cell types that are defined by differentiation states, genetic mutations and altered epigenetic programmes that impart functional diversity to individual cells. Elevated tumour cell heterogeneity is linked with progression, therapy resistance and relapse. Yet, ima...

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Autores principales: Tang, Qin, Moore, John C., Ignatius, Myron S., Tenente, Inês M., Hayes, Madeline N., Garcia, Elaine G., Torres Yordán, Nora, Bourque, Caitlin, He, Shuning, Blackburn, Jessica S., Look, A. Thomas, Houvras, Yariv, Langenau, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735845/
https://www.ncbi.nlm.nih.gov/pubmed/26790525
http://dx.doi.org/10.1038/ncomms10358
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author Tang, Qin
Moore, John C.
Ignatius, Myron S.
Tenente, Inês M.
Hayes, Madeline N.
Garcia, Elaine G.
Torres Yordán, Nora
Bourque, Caitlin
He, Shuning
Blackburn, Jessica S.
Look, A. Thomas
Houvras, Yariv
Langenau, David M.
author_facet Tang, Qin
Moore, John C.
Ignatius, Myron S.
Tenente, Inês M.
Hayes, Madeline N.
Garcia, Elaine G.
Torres Yordán, Nora
Bourque, Caitlin
He, Shuning
Blackburn, Jessica S.
Look, A. Thomas
Houvras, Yariv
Langenau, David M.
author_sort Tang, Qin
collection PubMed
description Cancers contain a wide diversity of cell types that are defined by differentiation states, genetic mutations and altered epigenetic programmes that impart functional diversity to individual cells. Elevated tumour cell heterogeneity is linked with progression, therapy resistance and relapse. Yet, imaging of tumour cell heterogeneity and the hallmarks of cancer has been a technical and biological challenge. Here we develop optically clear immune-compromised rag2(E450fs) (casper) zebrafish for optimized cell transplantation and direct visualization of fluorescently labelled cancer cells at single-cell resolution. Tumour engraftment permits dynamic imaging of neovascularization, niche partitioning of tumour-propagating cells in embryonal rhabdomyosarcoma, emergence of clonal dominance in T-cell acute lymphoblastic leukaemia and tumour evolution resulting in elevated growth and metastasis in BRAF(V600E)-driven melanoma. Cell transplantation approaches using optically clear immune-compromised zebrafish provide unique opportunities to uncover biology underlying cancer and to dynamically visualize cancer processes at single-cell resolution in vivo.
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spelling pubmed-47358452016-03-04 Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish Tang, Qin Moore, John C. Ignatius, Myron S. Tenente, Inês M. Hayes, Madeline N. Garcia, Elaine G. Torres Yordán, Nora Bourque, Caitlin He, Shuning Blackburn, Jessica S. Look, A. Thomas Houvras, Yariv Langenau, David M. Nat Commun Article Cancers contain a wide diversity of cell types that are defined by differentiation states, genetic mutations and altered epigenetic programmes that impart functional diversity to individual cells. Elevated tumour cell heterogeneity is linked with progression, therapy resistance and relapse. Yet, imaging of tumour cell heterogeneity and the hallmarks of cancer has been a technical and biological challenge. Here we develop optically clear immune-compromised rag2(E450fs) (casper) zebrafish for optimized cell transplantation and direct visualization of fluorescently labelled cancer cells at single-cell resolution. Tumour engraftment permits dynamic imaging of neovascularization, niche partitioning of tumour-propagating cells in embryonal rhabdomyosarcoma, emergence of clonal dominance in T-cell acute lymphoblastic leukaemia and tumour evolution resulting in elevated growth and metastasis in BRAF(V600E)-driven melanoma. Cell transplantation approaches using optically clear immune-compromised zebrafish provide unique opportunities to uncover biology underlying cancer and to dynamically visualize cancer processes at single-cell resolution in vivo. Nature Publishing Group 2016-01-21 /pmc/articles/PMC4735845/ /pubmed/26790525 http://dx.doi.org/10.1038/ncomms10358 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tang, Qin
Moore, John C.
Ignatius, Myron S.
Tenente, Inês M.
Hayes, Madeline N.
Garcia, Elaine G.
Torres Yordán, Nora
Bourque, Caitlin
He, Shuning
Blackburn, Jessica S.
Look, A. Thomas
Houvras, Yariv
Langenau, David M.
Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish
title Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish
title_full Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish
title_fullStr Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish
title_full_unstemmed Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish
title_short Imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish
title_sort imaging tumour cell heterogeneity following cell transplantation into optically clear immune-deficient zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735845/
https://www.ncbi.nlm.nih.gov/pubmed/26790525
http://dx.doi.org/10.1038/ncomms10358
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