Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic Tomography

PURPOSE: Here we demonstrate the potential of multispectral optoacoustic tomography (MSOT), a new non-invasive structural and functional imaging modality, to track the growth and changes in blood oxygen saturation (sO2) in orthotopic glioblastoma (GBMs) and the surrounding brain tissues upon adminis...

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Main Authors: Ghayathri Balasundaram, Lu Ding, Xiuting Li, Amalina Binte Ebrahim Attia, Xose Luis Dean-Ben, Chris Jun Hui Ho, Prashant Chandrasekharan, Hui Chien Tay, Hann Qian Lim, Chee Bing Ong, Ralph P. Mason, Daniel Razansky, Malini Olivo
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Translational Oncology
Online Access:http://www.sciencedirect.com/science/article/pii/S1936523318301591
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language English
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author Ghayathri Balasundaram
Lu Ding
Xiuting Li
Amalina Binte Ebrahim Attia
Xose Luis Dean-Ben
Chris Jun Hui Ho
Prashant Chandrasekharan
Hui Chien Tay
Hann Qian Lim
Chee Bing Ong
Ralph P. Mason
Daniel Razansky
Malini Olivo
spellingShingle Ghayathri Balasundaram
Lu Ding
Xiuting Li
Amalina Binte Ebrahim Attia
Xose Luis Dean-Ben
Chris Jun Hui Ho
Prashant Chandrasekharan
Hui Chien Tay
Hann Qian Lim
Chee Bing Ong
Ralph P. Mason
Daniel Razansky
Malini Olivo
Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic Tomography
Translational Oncology
author_facet Ghayathri Balasundaram
Lu Ding
Xiuting Li
Amalina Binte Ebrahim Attia
Xose Luis Dean-Ben
Chris Jun Hui Ho
Prashant Chandrasekharan
Hui Chien Tay
Hann Qian Lim
Chee Bing Ong
Ralph P. Mason
Daniel Razansky
Malini Olivo
author_sort Ghayathri Balasundaram
title Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic Tomography
title_short Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic Tomography
title_full Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic Tomography
title_fullStr Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic Tomography
title_full_unstemmed Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic Tomography
title_sort noninvasive anatomical and functional imaging of orthotopic glioblastoma development and therapy using multispectral optoacoustic tomography
publisher Elsevier
series Translational Oncology
issn 1936-5233
publishDate 2018-10-01
description PURPOSE: Here we demonstrate the potential of multispectral optoacoustic tomography (MSOT), a new non-invasive structural and functional imaging modality, to track the growth and changes in blood oxygen saturation (sO2) in orthotopic glioblastoma (GBMs) and the surrounding brain tissues upon administration of a vascular disruptive agent (VDA). METHODS: Nude mice injected with U87MG tumor cells were longitudinally monitored for the development of orthotopic GBMs up to 15 days and observed for changes in sO2 upon administration of combretastatin A4 phosphate (CA4P, 30 mg/kg), an FDA approved VDA for treating solid tumors. We employed a newly-developed non-negative constrained approach for combined MSOT image reconstruction and unmixing in order to quantitatively map sO2 in whole mouse brains. RESULTS: Upon longitudinal monitoring, tumors could be detected in mouse brains using single-wavelength data as early as 6 days post tumor cell inoculation. Fifteen days post-inoculation, tumors had higher sO2 of 63 ± 11% (n = 5, P < .05) against 48 ± 7% in the corresponding contralateral brain, indicating their hyperoxic status. In a different set of animals, 42 days post-inoculation, tumors had lower sO2 of 42 ± 5% against 49 ± 4% (n = 3, P < .05) in the contralateral side, indicating their hypoxic status. Upon CA4P administration, sO2 in 15 days post-inoculation tumors dropped from 61 ± 9% to 36 ± 1% (n = 4, P < .01) within one hour, then reverted to pre CA4P treatment values (63 ± 6%) and remained constant until the last observation time point of 6 hours. CONCLUSION: With the help of advanced post processing algorithms, MSOT was capable of monitoring the tumor growth and assessing hemodynamic changes upon administration of VDAs in orthotopic GBMs.
url http://www.sciencedirect.com/science/article/pii/S1936523318301591
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spelling doaj-3702cdc6201646e2aded24da666daf772020-11-24T21:05:22ZengElsevierTranslational Oncology1936-52332018-10-0111512511258Noninvasive Anatomical and Functional Imaging of Orthotopic Glioblastoma Development and Therapy using Multispectral Optoacoustic TomographyGhayathri Balasundaram0Lu Ding1Xiuting Li2Amalina Binte Ebrahim Attia3Xose Luis Dean-Ben4Chris Jun Hui Ho5Prashant Chandrasekharan6Hui Chien Tay7Hann Qian Lim8Chee Bing Ong9Ralph P. Mason10Daniel Razansky11Malini Olivo12Laboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667Institute for Biological and Medical Imaging, Technical University of Munich and Helmholtz Center Munich, Munich, GermanyLaboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667Laboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667Institute for Biological and Medical Imaging, Technical University of Munich and Helmholtz Center Munich, Munich, GermanyLaboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667Laboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667Laboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667Laboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667Advanced Molecular Pathology Lab (AMPL), Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), 61 Biopolis Drive, Proteos building, Singapore 138673Department of Radiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USAInstitute for Biological and Medical Imaging, Technical University of Munich and Helmholtz Center Munich, Munich, Germany; Address all correspondence to: Daniel Razansky or Malini Olivo.Laboratory of Bio-optical Imaging, Singapore Bioimaging Consortium, Agency for Science Technology and Research (A*STAR), 11 Biopolis Way, #02-02 Helios, Singapore 138667; Address all correspondence to: Daniel Razansky or Malini Olivo.PURPOSE: Here we demonstrate the potential of multispectral optoacoustic tomography (MSOT), a new non-invasive structural and functional imaging modality, to track the growth and changes in blood oxygen saturation (sO2) in orthotopic glioblastoma (GBMs) and the surrounding brain tissues upon administration of a vascular disruptive agent (VDA). METHODS: Nude mice injected with U87MG tumor cells were longitudinally monitored for the development of orthotopic GBMs up to 15 days and observed for changes in sO2 upon administration of combretastatin A4 phosphate (CA4P, 30 mg/kg), an FDA approved VDA for treating solid tumors. We employed a newly-developed non-negative constrained approach for combined MSOT image reconstruction and unmixing in order to quantitatively map sO2 in whole mouse brains. RESULTS: Upon longitudinal monitoring, tumors could be detected in mouse brains using single-wavelength data as early as 6 days post tumor cell inoculation. Fifteen days post-inoculation, tumors had higher sO2 of 63 ± 11% (n = 5, P < .05) against 48 ± 7% in the corresponding contralateral brain, indicating their hyperoxic status. In a different set of animals, 42 days post-inoculation, tumors had lower sO2 of 42 ± 5% against 49 ± 4% (n = 3, P < .05) in the contralateral side, indicating their hypoxic status. Upon CA4P administration, sO2 in 15 days post-inoculation tumors dropped from 61 ± 9% to 36 ± 1% (n = 4, P < .01) within one hour, then reverted to pre CA4P treatment values (63 ± 6%) and remained constant until the last observation time point of 6 hours. CONCLUSION: With the help of advanced post processing algorithms, MSOT was capable of monitoring the tumor growth and assessing hemodynamic changes upon administration of VDAs in orthotopic GBMs.http://www.sciencedirect.com/science/article/pii/S1936523318301591