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Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study
Combretastatin-A4-phosphate (CA4P) acts most effectively against immature tumour vasculature. We investigated whether histological angiogenic profile can explain the differential sensitivity of human tumours to CA4P, by correlating the kinetic changes demonstrated by dynamic MRI (DCE-MRI) in respons...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480970/ https://www.ncbi.nlm.nih.gov/pubmed/18612312 http://dx.doi.org/10.1038/sj.bjc.6604426 |
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author | Gaya, A Daley, F Taylor, N J Tozer, G Qureshi, U Padhani, A Pedley, R B Begent, R Wellsted, D Stirling, J J Rustin, G |
author_facet | Gaya, A Daley, F Taylor, N J Tozer, G Qureshi, U Padhani, A Pedley, R B Begent, R Wellsted, D Stirling, J J Rustin, G |
author_sort | Gaya, A |
collection | PubMed |
description | Combretastatin-A4-phosphate (CA4P) acts most effectively against immature tumour vasculature. We investigated whether histological angiogenic profile can explain the differential sensitivity of human tumours to CA4P, by correlating the kinetic changes demonstrated by dynamic MRI (DCE-MRI) in response to CA4P, with tumour immunohistochemical angiogenic markers. Tissue was received from 24 patients (mean age 59, range 32–73, 18 women, 6 men). An angiogenic profile was performed using standard immunohistochemical techniques. Dynamic MRI data were obtained for the same patients before and 4 h after CA4P. Three patients showed a statistically significant fall in K(trans) following CA4P, and one a statistically significant fall in IAUGC(60). No statistically significant correlations were seen between the continuous or categorical variables and the DCE-MRI kinetic parameters other than between ang-2 and K(trans) (P=0.044). In conclusion, we found no strong relationships between changes in DCE-MRI kinetic variables following CA4P and the immunohistochemical angiogenic profile. |
format | Text |
id | pubmed-2480970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24809702009-09-11 Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study Gaya, A Daley, F Taylor, N J Tozer, G Qureshi, U Padhani, A Pedley, R B Begent, R Wellsted, D Stirling, J J Rustin, G Br J Cancer Molecular Diagnostics Combretastatin-A4-phosphate (CA4P) acts most effectively against immature tumour vasculature. We investigated whether histological angiogenic profile can explain the differential sensitivity of human tumours to CA4P, by correlating the kinetic changes demonstrated by dynamic MRI (DCE-MRI) in response to CA4P, with tumour immunohistochemical angiogenic markers. Tissue was received from 24 patients (mean age 59, range 32–73, 18 women, 6 men). An angiogenic profile was performed using standard immunohistochemical techniques. Dynamic MRI data were obtained for the same patients before and 4 h after CA4P. Three patients showed a statistically significant fall in K(trans) following CA4P, and one a statistically significant fall in IAUGC(60). No statistically significant correlations were seen between the continuous or categorical variables and the DCE-MRI kinetic parameters other than between ang-2 and K(trans) (P=0.044). In conclusion, we found no strong relationships between changes in DCE-MRI kinetic variables following CA4P and the immunohistochemical angiogenic profile. Nature Publishing Group 2008-07-22 2008-07-08 /pmc/articles/PMC2480970/ /pubmed/18612312 http://dx.doi.org/10.1038/sj.bjc.6604426 Text en Copyright © 2008 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 Diagnostics Gaya, A Daley, F Taylor, N J Tozer, G Qureshi, U Padhani, A Pedley, R B Begent, R Wellsted, D Stirling, J J Rustin, G Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study |
title | Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study |
title_full | Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study |
title_fullStr | Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study |
title_full_unstemmed | Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study |
title_short | Relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study |
title_sort | relationship between human tumour angiogenic profile and combretastatin-induced vascular shutdown: an exploratory study |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480970/ https://www.ncbi.nlm.nih.gov/pubmed/18612312 http://dx.doi.org/10.1038/sj.bjc.6604426 |
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