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Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours

Stem cells have been utilised as anti-cancer agents due to their ability to home to and integrate within tumours. Methods to augment stem cell homing to tumours are being investigated with the goal of enhancing treatment efficacy. However, it is currently not possible to evaluate both cell localisat...

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Autores principales: Zaw Thin, May, Allan, Helen, Bofinger, Robin, Kostelec, Tomas D., Guillaume, Simon, Connell, John J., Patrick, P. Stephen, Hailes, Helen C., Tabor, Alethea B., Lythgoe, Mark F., Stuckey, Daniel J., Kalber, Tammy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586303/
https://www.ncbi.nlm.nih.gov/pubmed/32749427
http://dx.doi.org/10.1039/d0nr03237a
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author Zaw Thin, May
Allan, Helen
Bofinger, Robin
Kostelec, Tomas D.
Guillaume, Simon
Connell, John J.
Patrick, P. Stephen
Hailes, Helen C.
Tabor, Alethea B.
Lythgoe, Mark F.
Stuckey, Daniel J.
Kalber, Tammy L.
author_facet Zaw Thin, May
Allan, Helen
Bofinger, Robin
Kostelec, Tomas D.
Guillaume, Simon
Connell, John J.
Patrick, P. Stephen
Hailes, Helen C.
Tabor, Alethea B.
Lythgoe, Mark F.
Stuckey, Daniel J.
Kalber, Tammy L.
author_sort Zaw Thin, May
collection PubMed
description Stem cells have been utilised as anti-cancer agents due to their ability to home to and integrate within tumours. Methods to augment stem cell homing to tumours are being investigated with the goal of enhancing treatment efficacy. However, it is currently not possible to evaluate both cell localisation and cell viability after engraftment, hindering optimisation of therapy. In this study, luciferase-expressing human adipocyte-derived stem cells (ADSCs) were incubated with Indium-111 radiolabelled iron oxide nanoparticles to produce cells with tri-modal imaging capabilities. ADSCs were administered intravenously (IV) or intracardially (IC) to mice bearing orthotopic breast tumours. Cell fate was monitored using bioluminescence imaging (BLI) as a measure of cell viability, magnetic resonance imaging (MRI) for cell localisation and single photon emission computer tomography (SPECT) for cell quantification. Serial monitoring with multi-modal imaging showed the presence of viable ADSCs within tumours as early as 1-hour post IC injection and the percentage of ADSCs within tumours to be 2-fold higher after IC than IV. Finally, histological analysis was used to validate engraftment of ADSC within tumour tissue. These findings demonstrate that multi-modal imaging can be used to evaluate the efficiency of stem cell delivery to tumours and that IC cell administration is more effective for tumour targeting.
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spelling pubmed-75863032020-11-02 Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours Zaw Thin, May Allan, Helen Bofinger, Robin Kostelec, Tomas D. Guillaume, Simon Connell, John J. Patrick, P. Stephen Hailes, Helen C. Tabor, Alethea B. Lythgoe, Mark F. Stuckey, Daniel J. Kalber, Tammy L. Nanoscale Chemistry Stem cells have been utilised as anti-cancer agents due to their ability to home to and integrate within tumours. Methods to augment stem cell homing to tumours are being investigated with the goal of enhancing treatment efficacy. However, it is currently not possible to evaluate both cell localisation and cell viability after engraftment, hindering optimisation of therapy. In this study, luciferase-expressing human adipocyte-derived stem cells (ADSCs) were incubated with Indium-111 radiolabelled iron oxide nanoparticles to produce cells with tri-modal imaging capabilities. ADSCs were administered intravenously (IV) or intracardially (IC) to mice bearing orthotopic breast tumours. Cell fate was monitored using bioluminescence imaging (BLI) as a measure of cell viability, magnetic resonance imaging (MRI) for cell localisation and single photon emission computer tomography (SPECT) for cell quantification. Serial monitoring with multi-modal imaging showed the presence of viable ADSCs within tumours as early as 1-hour post IC injection and the percentage of ADSCs within tumours to be 2-fold higher after IC than IV. Finally, histological analysis was used to validate engraftment of ADSC within tumour tissue. These findings demonstrate that multi-modal imaging can be used to evaluate the efficiency of stem cell delivery to tumours and that IC cell administration is more effective for tumour targeting. Royal Society of Chemistry 2020-08-21 2020-08-04 /pmc/articles/PMC7586303/ /pubmed/32749427 http://dx.doi.org/10.1039/d0nr03237a Text en This journal is © The Royal Society of Chemistry 2020 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Zaw Thin, May
Allan, Helen
Bofinger, Robin
Kostelec, Tomas D.
Guillaume, Simon
Connell, John J.
Patrick, P. Stephen
Hailes, Helen C.
Tabor, Alethea B.
Lythgoe, Mark F.
Stuckey, Daniel J.
Kalber, Tammy L.
Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours
title Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours
title_full Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours
title_fullStr Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours
title_full_unstemmed Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours
title_short Multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours
title_sort multi-modal imaging probe for assessing the efficiency of stem cell delivery to orthotopic breast tumours
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586303/
https://www.ncbi.nlm.nih.gov/pubmed/32749427
http://dx.doi.org/10.1039/d0nr03237a
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