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Estimating oxygen distribution from vasculature in three-dimensional tumour tissue
Regions of tissue which are well oxygenated respond better to radiotherapy than hypoxic regions by up to a factor of three. If these volumes could be accurately estimated, then it might be possible to selectively boost dose to radio-resistant regions, a concept known as dose-painting. While imaging...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4843681/ https://www.ncbi.nlm.nih.gov/pubmed/26935806 http://dx.doi.org/10.1098/rsif.2016.0070 |
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author | Grimes, David Robert Kannan, Pavitra Warren, Daniel R. Markelc, Bostjan Bates, Russell Muschel, Ruth Partridge, Mike |
author_facet | Grimes, David Robert Kannan, Pavitra Warren, Daniel R. Markelc, Bostjan Bates, Russell Muschel, Ruth Partridge, Mike |
author_sort | Grimes, David Robert |
collection | PubMed |
description | Regions of tissue which are well oxygenated respond better to radiotherapy than hypoxic regions by up to a factor of three. If these volumes could be accurately estimated, then it might be possible to selectively boost dose to radio-resistant regions, a concept known as dose-painting. While imaging modalities such as (18)F-fluoromisonidazole positron emission tomography (PET) allow identification of hypoxic regions, they are intrinsically limited by the physics of such systems to the millimetre domain, whereas tumour oxygenation is known to vary over a micrometre scale. Mathematical modelling of microscopic tumour oxygen distribution therefore has the potential to complement and enhance macroscopic information derived from PET. In this work, we develop a general method of estimating oxygen distribution in three dimensions from a source vessel map. The method is applied analytically to line sources and quasi-linear idealized line source maps, and also applied to full three-dimensional vessel distributions through a kernel method and compared with oxygen distribution in tumour sections. The model outlined is flexible and stable, and can readily be applied to estimating likely microscopic oxygen distribution from any source geometry. We also investigate the problem of reconstructing three-dimensional oxygen maps from histological and confocal two-dimensional sections, concluding that two-dimensional histological sections are generally inadequate representations of the three-dimensional oxygen distribution. |
format | Online Article Text |
id | pubmed-4843681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48436812016-04-26 Estimating oxygen distribution from vasculature in three-dimensional tumour tissue Grimes, David Robert Kannan, Pavitra Warren, Daniel R. Markelc, Bostjan Bates, Russell Muschel, Ruth Partridge, Mike J R Soc Interface Life Sciences–Physics interface Regions of tissue which are well oxygenated respond better to radiotherapy than hypoxic regions by up to a factor of three. If these volumes could be accurately estimated, then it might be possible to selectively boost dose to radio-resistant regions, a concept known as dose-painting. While imaging modalities such as (18)F-fluoromisonidazole positron emission tomography (PET) allow identification of hypoxic regions, they are intrinsically limited by the physics of such systems to the millimetre domain, whereas tumour oxygenation is known to vary over a micrometre scale. Mathematical modelling of microscopic tumour oxygen distribution therefore has the potential to complement and enhance macroscopic information derived from PET. In this work, we develop a general method of estimating oxygen distribution in three dimensions from a source vessel map. The method is applied analytically to line sources and quasi-linear idealized line source maps, and also applied to full three-dimensional vessel distributions through a kernel method and compared with oxygen distribution in tumour sections. The model outlined is flexible and stable, and can readily be applied to estimating likely microscopic oxygen distribution from any source geometry. We also investigate the problem of reconstructing three-dimensional oxygen maps from histological and confocal two-dimensional sections, concluding that two-dimensional histological sections are generally inadequate representations of the three-dimensional oxygen distribution. The Royal Society 2016-03 /pmc/articles/PMC4843681/ /pubmed/26935806 http://dx.doi.org/10.1098/rsif.2016.0070 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Physics interface Grimes, David Robert Kannan, Pavitra Warren, Daniel R. Markelc, Bostjan Bates, Russell Muschel, Ruth Partridge, Mike Estimating oxygen distribution from vasculature in three-dimensional tumour tissue |
title | Estimating oxygen distribution from vasculature in three-dimensional tumour tissue |
title_full | Estimating oxygen distribution from vasculature in three-dimensional tumour tissue |
title_fullStr | Estimating oxygen distribution from vasculature in three-dimensional tumour tissue |
title_full_unstemmed | Estimating oxygen distribution from vasculature in three-dimensional tumour tissue |
title_short | Estimating oxygen distribution from vasculature in three-dimensional tumour tissue |
title_sort | estimating oxygen distribution from vasculature in three-dimensional tumour tissue |
topic | Life Sciences–Physics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4843681/ https://www.ncbi.nlm.nih.gov/pubmed/26935806 http://dx.doi.org/10.1098/rsif.2016.0070 |
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