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Sauerwein, Wolfgang A. G. Neutron Therapy Research Center, Okayama University
Sancey, Lucie UGA/Inserm U 1209/CNRS UMR 5309 Joint Research Center, Institute for Advanced Biosciences
Hey-Hawkins, Evamarie Deutsche Gesellschaft für Bor-Neutroneneinfangtherapie DGBNCT e.V.
Kellert, Martin Institute of Inorganic Chemistry, Department of Chemistry and Mineralogy, University Leipzig
Panza, Luigi Deutsche Gesellschaft für Bor-Neutroneneinfangtherapie DGBNCT e.V.
Imperio, Daniela Deutsche Gesellschaft für Bor-Neutroneneinfangtherapie DGBNCT e.V.
Balcerzyk, Marcin Departamento de Fisiología Medica y Biofísica, Universidad de Sevilla
Rizzo, Giovanna Institute for Biomedical Technologies (ITB-CNR)
Scalco, Elisa Institute for Biomedical Technologies (ITB-CNR)
Herrmann, Ken Department for Nuclear Medicine, University Hospital Essen
Mauri, Pierluigi Deutsche Gesellschaft für Bor-Neutroneneinfangtherapie DGBNCT e.V.
De Palma, Antonella Proteomics and Metabolomics Laboratory, ELIXIR Infrastructure, National Research Council (ITB-CNR)
Wittig, Andrea Deutsche Gesellschaft für Bor-Neutroneneinfangtherapie DGBNCT e.V.
Abstract
Boron neutron capture therapy (BNCT) has the potential to specifically destroy tumor cells without damaging the tissues infiltrated by the tumor. BNCT is a binary treatment method based on the combination of two agents that have no effect when applied individually: B-10 and thermal neutrons. Exclusively, the combination of both produces an effect, whose extent depends on the amount of B-10 in the tumor but also on the organs at risk. It is not yet possible to determine the B-10 concentration in a specific tissue using non-invasive methods. At present, it is only possible to measure the B-10 concentration in blood and to estimate the boron concentration in tissues based on the assumption that there is a fixed uptake of B-10 from the blood into tissues. On this imprecise assumption, BNCT can hardly be developed further. A therapeutic approach, combining the boron carrier for therapeutic purposes with an imaging tool, might allow us to determine the B-10 concentration in a specific tissue using a non-invasive method. This review provides an overview of the current clinical protocols and preclinical experiments and results on how innovative drug development for boron delivery systems can also incorporate concurrent imaging. The last section focuses on the importance of proteomics for further optimization of BNCT, a highly precise and personalized therapeutic approach.
Keywords
BNCT
radiation oncology
small molecules
BSH
BPA
PET
quantitative MRI
image registration
cell-penetrating peptides CPP
proteomics
Published Date
2021-04-10
Publication Title
Life-Basel
Volume
volume11
Issue
issue4
Publisher
MDPI
Start Page
330
ISSN
2075-1729
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
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publisher
PubMed ID
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Related Url
isVersionOf https://doi.org/10.3390/life11040330
License
https://creativecommons.org/licenses/by/4.0/