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Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence

BACKGROUND: Research using orthotopic and transgenic models of cancer requires imaging methods to non-invasively quantify tumour burden. As the choice of appropriate imaging modality is wide-ranging, this study aimed to compare low-field (1T) magnetic resonance imaging (MRI), a novel and relatively...

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Autores principales: Ramasawmy, Rajiv, Johnson, S. Peter, Roberts, Thomas A., Stuckey, Daniel J., David, Anna L., Pedley, R. Barbara, Lythgoe, Mark F., Siow, Bernard, Walker-Samuel, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880291/
https://www.ncbi.nlm.nih.gov/pubmed/27223614
http://dx.doi.org/10.1371/journal.pone.0156162
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author Ramasawmy, Rajiv
Johnson, S. Peter
Roberts, Thomas A.
Stuckey, Daniel J.
David, Anna L.
Pedley, R. Barbara
Lythgoe, Mark F.
Siow, Bernard
Walker-Samuel, Simon
author_facet Ramasawmy, Rajiv
Johnson, S. Peter
Roberts, Thomas A.
Stuckey, Daniel J.
David, Anna L.
Pedley, R. Barbara
Lythgoe, Mark F.
Siow, Bernard
Walker-Samuel, Simon
author_sort Ramasawmy, Rajiv
collection PubMed
description BACKGROUND: Research using orthotopic and transgenic models of cancer requires imaging methods to non-invasively quantify tumour burden. As the choice of appropriate imaging modality is wide-ranging, this study aimed to compare low-field (1T) magnetic resonance imaging (MRI), a novel and relatively low-cost system, against established preclinical techniques: bioluminescence imaging (BLI), ultrasound imaging (US), and high-field (9.4T) MRI. METHODS: A model of colorectal metastasis to the liver was established in eight mice, which were imaged with each modality over four weeks post-implantation. Tumour burden was assessed from manually segmented regions. RESULTS: All four imaging systems provided sufficient contrast to detect tumours in all of the mice after two weeks. No significant difference was detected between tumour doubling times estimated by low-field MRI, ultrasound imaging or high-field MRI. A strong correlation was measured between high-field MRI estimates of tumour burden and all the other modalities (p < 0.001, Pearson). CONCLUSION: These results suggest that both low-field MRI and ultrasound imaging are accurate modalities for characterising the growth of preclinical tumour models.
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spelling pubmed-48802912016-06-09 Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence Ramasawmy, Rajiv Johnson, S. Peter Roberts, Thomas A. Stuckey, Daniel J. David, Anna L. Pedley, R. Barbara Lythgoe, Mark F. Siow, Bernard Walker-Samuel, Simon PLoS One Research Article BACKGROUND: Research using orthotopic and transgenic models of cancer requires imaging methods to non-invasively quantify tumour burden. As the choice of appropriate imaging modality is wide-ranging, this study aimed to compare low-field (1T) magnetic resonance imaging (MRI), a novel and relatively low-cost system, against established preclinical techniques: bioluminescence imaging (BLI), ultrasound imaging (US), and high-field (9.4T) MRI. METHODS: A model of colorectal metastasis to the liver was established in eight mice, which were imaged with each modality over four weeks post-implantation. Tumour burden was assessed from manually segmented regions. RESULTS: All four imaging systems provided sufficient contrast to detect tumours in all of the mice after two weeks. No significant difference was detected between tumour doubling times estimated by low-field MRI, ultrasound imaging or high-field MRI. A strong correlation was measured between high-field MRI estimates of tumour burden and all the other modalities (p < 0.001, Pearson). CONCLUSION: These results suggest that both low-field MRI and ultrasound imaging are accurate modalities for characterising the growth of preclinical tumour models. Public Library of Science 2016-05-25 /pmc/articles/PMC4880291/ /pubmed/27223614 http://dx.doi.org/10.1371/journal.pone.0156162 Text en © 2016 Ramasawmy et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ramasawmy, Rajiv
Johnson, S. Peter
Roberts, Thomas A.
Stuckey, Daniel J.
David, Anna L.
Pedley, R. Barbara
Lythgoe, Mark F.
Siow, Bernard
Walker-Samuel, Simon
Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence
title Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence
title_full Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence
title_fullStr Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence
title_full_unstemmed Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence
title_short Monitoring the Growth of an Orthotopic Tumour Xenograft Model: Multi-Modal Imaging Assessment with Benchtop MRI (1T), High-Field MRI (9.4T), Ultrasound and Bioluminescence
title_sort monitoring the growth of an orthotopic tumour xenograft model: multi-modal imaging assessment with benchtop mri (1t), high-field mri (9.4t), ultrasound and bioluminescence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880291/
https://www.ncbi.nlm.nih.gov/pubmed/27223614
http://dx.doi.org/10.1371/journal.pone.0156162
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