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Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data.
Flavone acetic acid (FAA) showed impressive effects against murine solid tumours but no activity in clinical studies. The mechanism of action in mice may involve damage to tumour vasculature or immunomodulation, and these effects may be species-specific. Alternatively, concentrations of FAA achieved...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977940/ https://www.ncbi.nlm.nih.gov/pubmed/1520597 |
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author | Maughan, T. S. Ward, R. Dennis, I. Honess, D. J. Workman, P. Bleehen, N. M. |
author_facet | Maughan, T. S. Ward, R. Dennis, I. Honess, D. J. Workman, P. Bleehen, N. M. |
author_sort | Maughan, T. S. |
collection | PubMed |
description | Flavone acetic acid (FAA) showed impressive effects against murine solid tumours but no activity in clinical studies. The mechanism of action in mice may involve damage to tumour vasculature or immunomodulation, and these effects may be species-specific. Alternatively, concentrations of FAA achieved in mouse tumours may be higher than in human tumours. It is important to resolve this issue since it raises important questions about the relevance of in vitro versus in vivo tumour screens and the development of FAA analogues. As part of a Cancer Research Campaign Phase II study of metastatic melanoma in which 8.4 g m-2 FAA was given as a 6 h infusion, six tumour biopsies were obtained from four patients. FAA tumour concentrations were determined by HPLC and compared with subcutaneous murine solid tumours within the same analytical laboratory. Tumour/plasma percentages (range 26-61%; mean +/- SD, 43.9 +/- 11.4%) were similar to those in mice, as was the area under the curve (AUC) extrapolated to infinity and the AUC above the putative activity threshold of 100 micrograms ml-1. We conclude that the exposure of drug-refractory human melanoma tissue to FAA was comparable to that of sensitive mouse tumours. This suggests that reduced penetration of FAA into human tumours is unlikely to explain the lack of antitumour activity observed in clinical studies and that differences in mechanism of action are predominant. |
format | Text |
id | pubmed-1977940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19779402009-09-10 Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data. Maughan, T. S. Ward, R. Dennis, I. Honess, D. J. Workman, P. Bleehen, N. M. Br J Cancer Research Article Flavone acetic acid (FAA) showed impressive effects against murine solid tumours but no activity in clinical studies. The mechanism of action in mice may involve damage to tumour vasculature or immunomodulation, and these effects may be species-specific. Alternatively, concentrations of FAA achieved in mouse tumours may be higher than in human tumours. It is important to resolve this issue since it raises important questions about the relevance of in vitro versus in vivo tumour screens and the development of FAA analogues. As part of a Cancer Research Campaign Phase II study of metastatic melanoma in which 8.4 g m-2 FAA was given as a 6 h infusion, six tumour biopsies were obtained from four patients. FAA tumour concentrations were determined by HPLC and compared with subcutaneous murine solid tumours within the same analytical laboratory. Tumour/plasma percentages (range 26-61%; mean +/- SD, 43.9 +/- 11.4%) were similar to those in mice, as was the area under the curve (AUC) extrapolated to infinity and the AUC above the putative activity threshold of 100 micrograms ml-1. We conclude that the exposure of drug-refractory human melanoma tissue to FAA was comparable to that of sensitive mouse tumours. This suggests that reduced penetration of FAA into human tumours is unlikely to explain the lack of antitumour activity observed in clinical studies and that differences in mechanism of action are predominant. Nature Publishing Group 1992-09 /pmc/articles/PMC1977940/ /pubmed/1520597 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 Maughan, T. S. Ward, R. Dennis, I. Honess, D. J. Workman, P. Bleehen, N. M. Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data. |
title | Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data. |
title_full | Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data. |
title_fullStr | Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data. |
title_full_unstemmed | Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data. |
title_short | Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse data. |
title_sort | tumour concentrations of flavone acetic acid (faa) in human melanoma: comparison with mouse data. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977940/ https://www.ncbi.nlm.nih.gov/pubmed/1520597 |
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