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Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours
Patients treated with tamoxifen (TAM) for primary breast cancer often manifest de novo or acquired resistance, possibly through changes in drug metabolism. Using solid-phase extraction methods and reversed-phase high-performance liquid chromatography separations, levels of TAM and metabolites 4-hydr...
Autores principales: | , , , |
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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/PMC2374506/ https://www.ncbi.nlm.nih.gov/pubmed/10817496 http://dx.doi.org/10.1054/bjoc.2000.1120 |
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author | MacCallum, J Cummings, J Dixon, J M Miller, W R |
author_facet | MacCallum, J Cummings, J Dixon, J M Miller, W R |
author_sort | MacCallum, J |
collection | PubMed |
description | Patients treated with tamoxifen (TAM) for primary breast cancer often manifest de novo or acquired resistance, possibly through changes in drug metabolism. Using solid-phase extraction methods and reversed-phase high-performance liquid chromatography separations, levels of TAM and metabolites 4-hydroxytamoxifen (4OH) and desmethyltamoxifen (DMT) have been measured in plasma and tumour tissue from breast cancer patients treated with TAM for at least 3 months. Patients were categorized into those with tumours responding to TAM and those showing de novo or acquired resistance. Levels of TAM, 4OH and DMT in both plasma and tissue samples were correlated with clinical response, length of treatment and patient weight. Interesting results included accumulation of 4OH in tumour tissues over time in all patients, with significance reached in the acquired resistance group. In addition, significantly lower levels of 4OH and DMT were found in plasma taken from responding patients after 3 months of treatment when compared to non-responding patients, and a small group of ER-poor patients showed significantly lower levels of all three species in plasma when compared to other patients. Whilst not explaining TAM resistance in all cases, these differences could account for the development of resistance to TAM treatment in certain subgroups of patients. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2374506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23745062009-09-10 Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours MacCallum, J Cummings, J Dixon, J M Miller, W R Br J Cancer Regular Article Patients treated with tamoxifen (TAM) for primary breast cancer often manifest de novo or acquired resistance, possibly through changes in drug metabolism. Using solid-phase extraction methods and reversed-phase high-performance liquid chromatography separations, levels of TAM and metabolites 4-hydroxytamoxifen (4OH) and desmethyltamoxifen (DMT) have been measured in plasma and tumour tissue from breast cancer patients treated with TAM for at least 3 months. Patients were categorized into those with tumours responding to TAM and those showing de novo or acquired resistance. Levels of TAM, 4OH and DMT in both plasma and tissue samples were correlated with clinical response, length of treatment and patient weight. Interesting results included accumulation of 4OH in tumour tissues over time in all patients, with significance reached in the acquired resistance group. In addition, significantly lower levels of 4OH and DMT were found in plasma taken from responding patients after 3 months of treatment when compared to non-responding patients, and a small group of ER-poor patients showed significantly lower levels of all three species in plasma when compared to other patients. Whilst not explaining TAM resistance in all cases, these differences could account for the development of resistance to TAM treatment in certain subgroups of patients. © 2000 Cancer Research Campaign Nature Publishing Group 2000-05 2000-04-27 /pmc/articles/PMC2374506/ /pubmed/10817496 http://dx.doi.org/10.1054/bjoc.2000.1120 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 MacCallum, J Cummings, J Dixon, J M Miller, W R Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours |
title | Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours |
title_full | Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours |
title_fullStr | Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours |
title_full_unstemmed | Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours |
title_short | Concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours |
title_sort | concentrations of tamoxifen and its major metabolites in hormone responsive and resistant breast tumours |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374506/ https://www.ncbi.nlm.nih.gov/pubmed/10817496 http://dx.doi.org/10.1054/bjoc.2000.1120 |
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