Cargando…
Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts.
A method is presented in this report for concurrent analysis of vascular architecture, blood perfusion and proliferation characteristics in whole-tumour cross-sections of human larynx carcinoma and glioblastoma xenografts. Tumours were implanted subcutaneously in nude mice. After i.v. injection with...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1998
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151270/ https://www.ncbi.nlm.nih.gov/pubmed/9459146 |
_version_ | 1782144713314271232 |
---|---|
author | Bussink, J. Kaanders, J. H. Rijken, P. F. Martindale, C. A. van der Kogel, A. J. |
author_facet | Bussink, J. Kaanders, J. H. Rijken, P. F. Martindale, C. A. van der Kogel, A. J. |
author_sort | Bussink, J. |
collection | PubMed |
description | A method is presented in this report for concurrent analysis of vascular architecture, blood perfusion and proliferation characteristics in whole-tumour cross-sections of human larynx carcinoma and glioblastoma xenografts. Tumours were implanted subcutaneously in nude mice. After i.v. injection with Hoechst 33342 and bromodeoxyuridine (BrdUrd) as perfusion and proliferation markers, animals were killed. An antiendothelial antibody (9F1) was used to delineate vascular structures. Cross-sections were analysed by a multistep immune staining and a computer-controlled microscope scanning method. Each tumour section was stained and scanned four times (Hoechst, 9F1, BrdUrd and Fast Blue for all nuclei). When these images were combined, vasculature, perfusion and proliferation parameters were analysed. The labelling index (LI) was defined as the ratio of the BrdUrd-labelled area to the total nuclear area. The LI based on manual counting and the LI calculated by flow cytometry (FCM) were in good agreement with the LI based on surface analysis. LI decreased at increasing distance from its nearest vessel. In the vicinity of perfused vessels, the LI was 30-70% higher than near non-perfused vessels. This method shows that both vasculature/perfusion and proliferation characteristics can be measured in the same whole-tumour section in a semiautomatic way. This could be applied in clinical practice to identify combined human tumour characteristics that predict for a favourable response to treatment modifications. IMAGES: |
format | Text |
id | pubmed-2151270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-21512702009-09-10 Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. Bussink, J. Kaanders, J. H. Rijken, P. F. Martindale, C. A. van der Kogel, A. J. Br J Cancer Research Article A method is presented in this report for concurrent analysis of vascular architecture, blood perfusion and proliferation characteristics in whole-tumour cross-sections of human larynx carcinoma and glioblastoma xenografts. Tumours were implanted subcutaneously in nude mice. After i.v. injection with Hoechst 33342 and bromodeoxyuridine (BrdUrd) as perfusion and proliferation markers, animals were killed. An antiendothelial antibody (9F1) was used to delineate vascular structures. Cross-sections were analysed by a multistep immune staining and a computer-controlled microscope scanning method. Each tumour section was stained and scanned four times (Hoechst, 9F1, BrdUrd and Fast Blue for all nuclei). When these images were combined, vasculature, perfusion and proliferation parameters were analysed. The labelling index (LI) was defined as the ratio of the BrdUrd-labelled area to the total nuclear area. The LI based on manual counting and the LI calculated by flow cytometry (FCM) were in good agreement with the LI based on surface analysis. LI decreased at increasing distance from its nearest vessel. In the vicinity of perfused vessels, the LI was 30-70% higher than near non-perfused vessels. This method shows that both vasculature/perfusion and proliferation characteristics can be measured in the same whole-tumour section in a semiautomatic way. This could be applied in clinical practice to identify combined human tumour characteristics that predict for a favourable response to treatment modifications. IMAGES: Nature Publishing Group 1998 /pmc/articles/PMC2151270/ /pubmed/9459146 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 Bussink, J. Kaanders, J. H. Rijken, P. F. Martindale, C. A. van der Kogel, A. J. Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. |
title | Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. |
title_full | Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. |
title_fullStr | Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. |
title_full_unstemmed | Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. |
title_short | Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. |
title_sort | multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151270/ https://www.ncbi.nlm.nih.gov/pubmed/9459146 |
work_keys_str_mv | AT bussinkj multiparameteranalysisofvasculatureperfusionandproliferationinhumantumourxenografts AT kaandersjh multiparameteranalysisofvasculatureperfusionandproliferationinhumantumourxenografts AT rijkenpf multiparameteranalysisofvasculatureperfusionandproliferationinhumantumourxenografts AT martindaleca multiparameteranalysisofvasculatureperfusionandproliferationinhumantumourxenografts AT vanderkogelaj multiparameteranalysisofvasculatureperfusionandproliferationinhumantumourxenografts |