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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4735845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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