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Angiogenic switch occurs late in squamous cell carcinomas of human skin
Angiogenesis is a crucial event in carcinogenesis and its onset has been associated with premalignant tumour stages. In order to elucidate the significance of angiogenesis in different stages of epithelial skin tumours, we analysed the vessel density in ten normal skin samples, 14 actinic keratosis...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363323/ https://www.ncbi.nlm.nih.gov/pubmed/10682671 http://dx.doi.org/10.1054/bjoc.1999.0969 |
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author | Strieth, S Hartschuh, W Pilz, L Fusenig, N E |
author_facet | Strieth, S Hartschuh, W Pilz, L Fusenig, N E |
author_sort | Strieth, S |
collection | PubMed |
description | Angiogenesis is a crucial event in carcinogenesis and its onset has been associated with premalignant tumour stages. In order to elucidate the significance of angiogenesis in different stages of epithelial skin tumours, we analysed the vessel density in ten normal skin samples, 14 actinic keratosis (AK), 12 hypertrophic AKs, and in nine early- and 16 late-stage squamous cell carcinomas (SCCs). Mean vascular density was quantitated by counting the number of CD 31-immunostained blood vessels and by morphometric assessment of stained vessel area by computer-assisted image analysis. The results from both methods were well correlated. Mean vascular density was similar in normal dermis and in AK, and only slightly elevated in hypertrophic AKs and early SCC stages (tumour thickness < 2 mm). Only late-stage SCCs infiltrating the subcutis exhibited a significant increase in vascularization. Vessel density was independent of tumour localization, degree of proliferation and inflammatory cell infiltration. Furthermore, tumour vascularization was not correlated with the expression of vascular endothelial growth factor, a major angiogenic factor, as revealed by in situ hybridization and immunohistochemistry. The restriction of enhanced vascularization to increased tumour thickness may be a major reason for the rather low metastatic spread of cutaneous SCCs. © 2000 CancerResearch Campaign |
format | Text |
id | pubmed-2363323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23633232009-09-10 Angiogenic switch occurs late in squamous cell carcinomas of human skin Strieth, S Hartschuh, W Pilz, L Fusenig, N E Br J Cancer Regular Article Angiogenesis is a crucial event in carcinogenesis and its onset has been associated with premalignant tumour stages. In order to elucidate the significance of angiogenesis in different stages of epithelial skin tumours, we analysed the vessel density in ten normal skin samples, 14 actinic keratosis (AK), 12 hypertrophic AKs, and in nine early- and 16 late-stage squamous cell carcinomas (SCCs). Mean vascular density was quantitated by counting the number of CD 31-immunostained blood vessels and by morphometric assessment of stained vessel area by computer-assisted image analysis. The results from both methods were well correlated. Mean vascular density was similar in normal dermis and in AK, and only slightly elevated in hypertrophic AKs and early SCC stages (tumour thickness < 2 mm). Only late-stage SCCs infiltrating the subcutis exhibited a significant increase in vascularization. Vessel density was independent of tumour localization, degree of proliferation and inflammatory cell infiltration. Furthermore, tumour vascularization was not correlated with the expression of vascular endothelial growth factor, a major angiogenic factor, as revealed by in situ hybridization and immunohistochemistry. The restriction of enhanced vascularization to increased tumour thickness may be a major reason for the rather low metastatic spread of cutaneous SCCs. © 2000 CancerResearch Campaign Nature Publishing Group 2000-02 2000-01-18 /pmc/articles/PMC2363323/ /pubmed/10682671 http://dx.doi.org/10.1054/bjoc.1999.0969 Text en Copyright © 2000 Cancer Research Campaign 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 | Regular Article Strieth, S Hartschuh, W Pilz, L Fusenig, N E Angiogenic switch occurs late in squamous cell carcinomas of human skin |
title | Angiogenic switch occurs late in squamous cell carcinomas of human skin |
title_full | Angiogenic switch occurs late in squamous cell carcinomas of human skin |
title_fullStr | Angiogenic switch occurs late in squamous cell carcinomas of human skin |
title_full_unstemmed | Angiogenic switch occurs late in squamous cell carcinomas of human skin |
title_short | Angiogenic switch occurs late in squamous cell carcinomas of human skin |
title_sort | angiogenic switch occurs late in squamous cell carcinomas of human skin |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363323/ https://www.ncbi.nlm.nih.gov/pubmed/10682671 http://dx.doi.org/10.1054/bjoc.1999.0969 |
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