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Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis
A number of laboratories are utilising both hypoxia and perfusion markers to spatially quantify tumour oxygenation and vascular distributions, and scientists are increasingly turning to automated image analysis methods to quantify such interrelationships. In these studies, the presence of regions of...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375413/ https://www.ncbi.nlm.nih.gov/pubmed/12087474 http://dx.doi.org/10.1038/sj.bjc.6600343 |
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author | Fenton, B M Paoni, S F Beauchamp, B K Ding, I |
author_facet | Fenton, B M Paoni, S F Beauchamp, B K Ding, I |
author_sort | Fenton, B M |
collection | PubMed |
description | A number of laboratories are utilising both hypoxia and perfusion markers to spatially quantify tumour oxygenation and vascular distributions, and scientists are increasingly turning to automated image analysis methods to quantify such interrelationships. In these studies, the presence of regions of necrosis in the immunohistochemical sections remains a potentially significant source of error. In the present work, frozen MCa-4 mammary tumour sections were used to obtain a series of corresponding image montages. Total vessels were identified using CD31 staining, perfused vessels by DiOC(7) staining, hypoxia by EF5/Cy3 uptake, and necrosis by haematoxylin and eosin staining. Our goal was to utilise image analysis techniques to spatially quantitate hypoxic marker binding as a function of distance from the nearest blood vessel. Several refinements to previous imaging methods are described: (1) hypoxia marker images are quantified in terms of their intensity levels, thus providing an analysis of the gradients in hypoxia with increasing distances from blood vessels, (2) zonal imaging masks are derived, which permit spatial sampling of images at precisely defined distances from blood vessels, as well as the omission of necrotic artifacts, (3) thresholding techniques are applied to omit holes in the tissue sections, and (4) distance mapping is utilised to define vascular spacing. British Journal of Cancer (2002) 86, 1831–1836. doi:10.1038/sj.bjc.6600343 www.bjcancer.com © 2002 Cancer Research UK |
format | Text |
id | pubmed-2375413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23754132009-09-10 Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis Fenton, B M Paoni, S F Beauchamp, B K Ding, I Br J Cancer Experimental Therapeutics A number of laboratories are utilising both hypoxia and perfusion markers to spatially quantify tumour oxygenation and vascular distributions, and scientists are increasingly turning to automated image analysis methods to quantify such interrelationships. In these studies, the presence of regions of necrosis in the immunohistochemical sections remains a potentially significant source of error. In the present work, frozen MCa-4 mammary tumour sections were used to obtain a series of corresponding image montages. Total vessels were identified using CD31 staining, perfused vessels by DiOC(7) staining, hypoxia by EF5/Cy3 uptake, and necrosis by haematoxylin and eosin staining. Our goal was to utilise image analysis techniques to spatially quantitate hypoxic marker binding as a function of distance from the nearest blood vessel. Several refinements to previous imaging methods are described: (1) hypoxia marker images are quantified in terms of their intensity levels, thus providing an analysis of the gradients in hypoxia with increasing distances from blood vessels, (2) zonal imaging masks are derived, which permit spatial sampling of images at precisely defined distances from blood vessels, as well as the omission of necrotic artifacts, (3) thresholding techniques are applied to omit holes in the tissue sections, and (4) distance mapping is utilised to define vascular spacing. British Journal of Cancer (2002) 86, 1831–1836. doi:10.1038/sj.bjc.6600343 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-06-05 /pmc/articles/PMC2375413/ /pubmed/12087474 http://dx.doi.org/10.1038/sj.bjc.6600343 Text en Copyright © 2002 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Experimental Therapeutics Fenton, B M Paoni, S F Beauchamp, B K Ding, I Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis |
title | Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis |
title_full | Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis |
title_fullStr | Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis |
title_full_unstemmed | Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis |
title_short | Zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis |
title_sort | zonal image analysis of tumour vascular perfusion, hypoxia, and necrosis |
topic | Experimental Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375413/ https://www.ncbi.nlm.nih.gov/pubmed/12087474 http://dx.doi.org/10.1038/sj.bjc.6600343 |
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