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Quantitative in vivo optical tomography of cancer progression & vasculature development in adult zebrafish

Quantitative in vivo optical tomography of cancer progression & vasculature development in adult zebrafish
Quantitative in vivo optical tomography of cancer progression & vasculature development in adult zebrafish

We describe a novel approach to study tumour progression and vasculature development in vivo via global 3-D fluorescence imaging of live non-pigmented adult zebrafish utilising angularly multiplexed optical projection tomography with compressive sensing (CS-OPT). This "mesoscopic" imaging method bridges a gap between established ~μm resolution 3-D fluorescence microscopy techniques and ~mm-resolved whole body planar imaging and diffuse tomography. Implementing angular multiplexing with CS-OPT, we demonstrate the in vivo global imaging of an inducible fluorescently labelled genetic model of liver cancer in adult non-pigmented zebrafish that also present fluorescently labelled vasculature. In this disease model, addition of a chemical inducer (doxycycline) drives expression of eGFP tagged oncogenic K-RASV12 in the liver of immune competent animals. We show that our novel in vivo global imaging methodology enables non-invasive quantitative imaging of the development of tumour and vasculature throughout the progression of the disease, which we have validated against established methods of pathology including immunohistochemistry. We have also demonstrated its potential for longitudinal imaging through a study of vascular development in the same zebrafish from early embryo to adulthood. We believe that this instrument, together with its associated analysis and data management tools, constitute a new platform for in vivo cancer studies and drug discovery in zebrafish disease models.

Animals, Animals, Genetically Modified, Disease Models, Animal, Disease Progression, Imaging, Three-Dimensional, Liver Neoplasms, Neovascularization, Pathologic, Tomography, Optical, Zebrafish, Journal Article
1949-2553
43939-43948
Kumar, Sunil
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Lockwood, Nicola
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Ramel, Marie-Christine
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Correia, Teresa
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Ellis, Matthew
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Alexandrov, Yuriy
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Andrews, Natalie
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Patel, Rachel
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Bugeon, Laurence
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Dallman, Margaret J
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Brandner, Sebastian
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Arridge, Simon
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Katan, Matilda
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McGinty, James
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Frankel, Paul
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French, Paul M W
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Kumar, Sunil
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Lockwood, Nicola
877cbbbc-68e3-4796-b828-56045ebe3070
Ramel, Marie-Christine
01c51f5b-04c1-43da-a12f-633f5493b3be
Correia, Teresa
ae436281-142d-44f0-bbfd-2038091beb91
Ellis, Matthew
afbca752-ced4-40dd-b0af-d9ecffbd5b63
Alexandrov, Yuriy
d47b8bbf-bf0d-40e4-a629-26e6f60d805a
Andrews, Natalie
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Patel, Rachel
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Bugeon, Laurence
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Dallman, Margaret J
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Brandner, Sebastian
f64b2397-fa45-4378-bf5a-1c6bbb14f18e
Arridge, Simon
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Katan, Matilda
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McGinty, James
1773dc55-78be-4ca0-bba5-db4c7a8cbf64
Frankel, Paul
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French, Paul M W
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Kumar, Sunil, Lockwood, Nicola, Ramel, Marie-Christine, Correia, Teresa, Ellis, Matthew, Alexandrov, Yuriy, Andrews, Natalie, Patel, Rachel, Bugeon, Laurence, Dallman, Margaret J, Brandner, Sebastian, Arridge, Simon, Katan, Matilda, McGinty, James, Frankel, Paul and French, Paul M W (2016) Quantitative in vivo optical tomography of cancer progression & vasculature development in adult zebrafish. Oncotarget, 7 (28), 43939-43948. (doi:10.18632/oncotarget.9756).

Record type: Article

Abstract

We describe a novel approach to study tumour progression and vasculature development in vivo via global 3-D fluorescence imaging of live non-pigmented adult zebrafish utilising angularly multiplexed optical projection tomography with compressive sensing (CS-OPT). This "mesoscopic" imaging method bridges a gap between established ~μm resolution 3-D fluorescence microscopy techniques and ~mm-resolved whole body planar imaging and diffuse tomography. Implementing angular multiplexing with CS-OPT, we demonstrate the in vivo global imaging of an inducible fluorescently labelled genetic model of liver cancer in adult non-pigmented zebrafish that also present fluorescently labelled vasculature. In this disease model, addition of a chemical inducer (doxycycline) drives expression of eGFP tagged oncogenic K-RASV12 in the liver of immune competent animals. We show that our novel in vivo global imaging methodology enables non-invasive quantitative imaging of the development of tumour and vasculature throughout the progression of the disease, which we have validated against established methods of pathology including immunohistochemistry. We have also demonstrated its potential for longitudinal imaging through a study of vascular development in the same zebrafish from early embryo to adulthood. We believe that this instrument, together with its associated analysis and data management tools, constitute a new platform for in vivo cancer studies and drug discovery in zebrafish disease models.

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e-pub ahead of print date: 1 June 2016
Published date: 12 July 2016
Keywords: Animals, Animals, Genetically Modified, Disease Models, Animal, Disease Progression, Imaging, Three-Dimensional, Liver Neoplasms, Neovascularization, Pathologic, Tomography, Optical, Zebrafish, Journal Article

Identifiers

Local EPrints ID: 428108
URI: http://eprints.soton.ac.uk/id/eprint/428108
ISSN: 1949-2553
PURE UUID: 91a93eca-4cf9-46d7-96a4-ff8f3934b775

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Date deposited: 11 Feb 2019 17:30
Last modified: 16 Mar 2024 00:08

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Contributors

Author: Sunil Kumar
Author: Nicola Lockwood
Author: Marie-Christine Ramel
Author: Teresa Correia
Author: Matthew Ellis
Author: Yuriy Alexandrov
Author: Natalie Andrews
Author: Rachel Patel
Author: Laurence Bugeon
Author: Margaret J Dallman
Author: Sebastian Brandner
Author: Simon Arridge
Author: Matilda Katan
Author: James McGinty
Author: Paul Frankel
Author: Paul M W French

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