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Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment

Assessment of microvessel density by immunohistochemical staining is subject to a considerable inter-observer variation, and this has led to variability in correlation between microvessel density and clinical outcome in different studies. In order to improve the method of microvessel density measure...

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Autores principales: Baeten, C I M, Wagstaff, J, Verhoeven, I C L, Hillen, H F P, Griffioen, A W
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364230/
https://www.ncbi.nlm.nih.gov/pubmed/12177806
http://dx.doi.org/10.1038/sj.bjc.6600457
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author Baeten, C I M
Wagstaff, J
Verhoeven, I C L
Hillen, H F P
Griffioen, A W
author_facet Baeten, C I M
Wagstaff, J
Verhoeven, I C L
Hillen, H F P
Griffioen, A W
author_sort Baeten, C I M
collection PubMed
description Assessment of microvessel density by immunohistochemical staining is subject to a considerable inter-observer variation, and this has led to variability in correlation between microvessel density and clinical outcome in different studies. In order to improve the method of microvessel density measurement in tumour biopsies, we have developed a rapid, objective and quantitative method using flow cytometry on frozen tissues. Frozen tissue sections of archival tumour material were enzymatically digested. The single-cell suspension was stained for CD31 and CD34 for flow cytometry. The number of endothelial cells was quantified using light scatter- and fluorescence-characteristics. Tumour endothelial cells were detectable in a single cell suspension, and the percentage of endothelial cells detected in 32 colon carcinomas correlated highly (r=0.84, P<0.001) with the immunohistochemical assessment of microvessel density. Flow cytometric endothelial cells quantification was found to be more sensitive especially at lower levels of immunohistochemical microvessel density measurement. The current method was found to be applicable for various tumour types and has the major advantage that it provides a retrospective and quantitative approach to the angiogenic potential of tumours. British Journal of Cancer (2002) 87, 344–347. doi:10.1038/sj.bjc.6600457 www.bjcancer.com © 2002 Cancer Research UK
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spelling pubmed-23642302009-09-10 Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment Baeten, C I M Wagstaff, J Verhoeven, I C L Hillen, H F P Griffioen, A W Br J Cancer Molecular and Cellular Pathology Assessment of microvessel density by immunohistochemical staining is subject to a considerable inter-observer variation, and this has led to variability in correlation between microvessel density and clinical outcome in different studies. In order to improve the method of microvessel density measurement in tumour biopsies, we have developed a rapid, objective and quantitative method using flow cytometry on frozen tissues. Frozen tissue sections of archival tumour material were enzymatically digested. The single-cell suspension was stained for CD31 and CD34 for flow cytometry. The number of endothelial cells was quantified using light scatter- and fluorescence-characteristics. Tumour endothelial cells were detectable in a single cell suspension, and the percentage of endothelial cells detected in 32 colon carcinomas correlated highly (r=0.84, P<0.001) with the immunohistochemical assessment of microvessel density. Flow cytometric endothelial cells quantification was found to be more sensitive especially at lower levels of immunohistochemical microvessel density measurement. The current method was found to be applicable for various tumour types and has the major advantage that it provides a retrospective and quantitative approach to the angiogenic potential of tumours. British Journal of Cancer (2002) 87, 344–347. doi:10.1038/sj.bjc.6600457 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-07-29 2002-08-01 /pmc/articles/PMC2364230/ /pubmed/12177806 http://dx.doi.org/10.1038/sj.bjc.6600457 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 Molecular and Cellular Pathology
Baeten, C I M
Wagstaff, J
Verhoeven, I C L
Hillen, H F P
Griffioen, A W
Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment
title Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment
title_full Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment
title_fullStr Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment
title_full_unstemmed Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment
title_short Flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment
title_sort flow cytometric quantification of tumour endothelial cells; an objective alternative for microvessel density assessment
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364230/
https://www.ncbi.nlm.nih.gov/pubmed/12177806
http://dx.doi.org/10.1038/sj.bjc.6600457
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