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Evidence for a weak angiogenic response to human colorectal cancers.
Many previous qualitative studies have shown that tumours are less vascular in the centre, and that host tissues become more vascular in close proximity to tumours. However, quantitative findings presented here for human colorectal cancer reveal some significant differences. Sections from 20 colorec...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033771/ https://www.ncbi.nlm.nih.gov/pubmed/7537517 |
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author | Pritchard, A. J. Chatterjee, T. Wilkinson, M. Powe, D. G. Gray, T. Hewitt, R. E. |
author_facet | Pritchard, A. J. Chatterjee, T. Wilkinson, M. Powe, D. G. Gray, T. Hewitt, R. E. |
author_sort | Pritchard, A. J. |
collection | PubMed |
description | Many previous qualitative studies have shown that tumours are less vascular in the centre, and that host tissues become more vascular in close proximity to tumours. However, quantitative findings presented here for human colorectal cancer reveal some significant differences. Sections from 20 colorectal carcinomas (ten moderately and ten poorly differentiated) were immunostained with the QB/end/10 monoclonal to demonstrate blood vessels. These were measured by interactive morphometry and vascular volume density, surface density (Sv) and length density were recorded. In poorly differentiated carcinomas, the tumour centre was significantly less vascular than the periphery for all three parameters (P = 0.008 for Sv). However, no significant difference was seen for moderately differentiated tumours, which constitute the majority of colorectal cancers. Surrounding host tissues did not show a general increase in vascular density close to tumours. Furthermore, when total viable tissue was considered, the vascular density of carcinomas was not markedly different from normal mucosa. In the centre of moderately differentiated carcinomas for example, the mean value for Sv was only 1.4 times higher than the mean value for normal mucosa. These findings suggest that colorectal cancers may elicit a relatively weak angiogenic response, consistent with their exceptionally slow growth rate. IMAGES: |
format | Text |
id | pubmed-2033771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20337712009-09-10 Evidence for a weak angiogenic response to human colorectal cancers. Pritchard, A. J. Chatterjee, T. Wilkinson, M. Powe, D. G. Gray, T. Hewitt, R. E. Br J Cancer Research Article Many previous qualitative studies have shown that tumours are less vascular in the centre, and that host tissues become more vascular in close proximity to tumours. However, quantitative findings presented here for human colorectal cancer reveal some significant differences. Sections from 20 colorectal carcinomas (ten moderately and ten poorly differentiated) were immunostained with the QB/end/10 monoclonal to demonstrate blood vessels. These were measured by interactive morphometry and vascular volume density, surface density (Sv) and length density were recorded. In poorly differentiated carcinomas, the tumour centre was significantly less vascular than the periphery for all three parameters (P = 0.008 for Sv). However, no significant difference was seen for moderately differentiated tumours, which constitute the majority of colorectal cancers. Surrounding host tissues did not show a general increase in vascular density close to tumours. Furthermore, when total viable tissue was considered, the vascular density of carcinomas was not markedly different from normal mucosa. In the centre of moderately differentiated carcinomas for example, the mean value for Sv was only 1.4 times higher than the mean value for normal mucosa. These findings suggest that colorectal cancers may elicit a relatively weak angiogenic response, consistent with their exceptionally slow growth rate. IMAGES: Nature Publishing Group 1995-05 /pmc/articles/PMC2033771/ /pubmed/7537517 Text en 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 | Research Article Pritchard, A. J. Chatterjee, T. Wilkinson, M. Powe, D. G. Gray, T. Hewitt, R. E. Evidence for a weak angiogenic response to human colorectal cancers. |
title | Evidence for a weak angiogenic response to human colorectal cancers. |
title_full | Evidence for a weak angiogenic response to human colorectal cancers. |
title_fullStr | Evidence for a weak angiogenic response to human colorectal cancers. |
title_full_unstemmed | Evidence for a weak angiogenic response to human colorectal cancers. |
title_short | Evidence for a weak angiogenic response to human colorectal cancers. |
title_sort | evidence for a weak angiogenic response to human colorectal cancers. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033771/ https://www.ncbi.nlm.nih.gov/pubmed/7537517 |
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