Imperial College London

ProfessorPaulFrench

Faculty of Natural SciencesDepartment of Physics

Professor of Physics and Vice Dean (Research) - FoNS
 
 
 
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Contact

 

+44 (0)20 7594 7706paul.french Website

 
 
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Assistant

 

Ms Judith Baylis +44 (0)20 7594 7713

 
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Location

 

609Blackett LaboratorySouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Kumar:2016:10.18632/oncotarget.9756,
author = {Kumar, S and Lockward, N and Ramel, M-C and Correia, T and Ellis, M and Alexandrov, Y and Andrews, N and Patel, R and Bugeon, L and Dallman, M and Brandner, S and Arridge, S and Katan, M and McGinty, J and Frankel, P and French, PMW},
doi = {10.18632/oncotarget.9756},
journal = {Oncotarget},
pages = {43939--43948},
title = {Quantitative in vivo optical tomography of cancer progression & vasculature development in adult zebrafish},
url = {http://dx.doi.org/10.18632/oncotarget.9756},
volume = {7},
year = {2016}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - 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.
AU - Kumar,S
AU - Lockward,N
AU - Ramel,M-C
AU - Correia,T
AU - Ellis,M
AU - Alexandrov,Y
AU - Andrews,N
AU - Patel,R
AU - Bugeon,L
AU - Dallman,M
AU - Brandner,S
AU - Arridge,S
AU - Katan,M
AU - McGinty,J
AU - Frankel,P
AU - French,PMW
DO - 10.18632/oncotarget.9756
EP - 43948
PY - 2016///
SN - 1949-2553
SP - 43939
TI - Quantitative in vivo optical tomography of cancer progression & vasculature development in adult zebrafish
T2 - Oncotarget
UR - http://dx.doi.org/10.18632/oncotarget.9756
UR - http://hdl.handle.net/10044/1/33325
VL - 7
ER -