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Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging
BACKGROUND: Tamoxifen is used in endocrine treatment of breast cancer to inhibit estrogen signaling. A set of stratified ER-positive and ER-negative tumor sections was subjected to manual deposition of tamoxifen solution in order to investigate its spatial distribution upon exposure to interaction w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786513/ https://www.ncbi.nlm.nih.gov/pubmed/26965929 http://dx.doi.org/10.1186/s40169-016-0090-9 |
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author | Végvári, Ákos Shavkunov, Alexander S. Fehniger, Thomas E. Grabau, Dorthe Niméus, Emma Marko-Varga, György |
author_facet | Végvári, Ákos Shavkunov, Alexander S. Fehniger, Thomas E. Grabau, Dorthe Niméus, Emma Marko-Varga, György |
author_sort | Végvári, Ákos |
collection | PubMed |
description | BACKGROUND: Tamoxifen is used in endocrine treatment of breast cancer to inhibit estrogen signaling. A set of stratified ER-positive and ER-negative tumor sections was subjected to manual deposition of tamoxifen solution in order to investigate its spatial distribution upon exposure to interaction within thin tissue sections. METHODS: The localization of tamoxifen in tumor sections was assessed by matrix assisted laser deposition/ionization mass spectrometry imaging. The images of extracted ion maps were analyzed for comparison of signal intensity distributions. RESULTS: The precursor ion of tamoxifen (m/z 372.233) displayed heterogeneous signal intensity distributions in histological compartments of tumor tissue sections. The levels of tamoxifen in tumor cells compared with stroma were higher in ER-positive tissues, whereas ER-negative tissue sections showed lower signal intensities in tumor cells. CONCLUSIONS: The experimental model was successfully applied on frozen tumor samples allowing for differentiation between ER groups based on distribution of tamoxifen. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40169-016-0090-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4786513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47865132016-04-09 Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging Végvári, Ákos Shavkunov, Alexander S. Fehniger, Thomas E. Grabau, Dorthe Niméus, Emma Marko-Varga, György Clin Transl Med Research BACKGROUND: Tamoxifen is used in endocrine treatment of breast cancer to inhibit estrogen signaling. A set of stratified ER-positive and ER-negative tumor sections was subjected to manual deposition of tamoxifen solution in order to investigate its spatial distribution upon exposure to interaction within thin tissue sections. METHODS: The localization of tamoxifen in tumor sections was assessed by matrix assisted laser deposition/ionization mass spectrometry imaging. The images of extracted ion maps were analyzed for comparison of signal intensity distributions. RESULTS: The precursor ion of tamoxifen (m/z 372.233) displayed heterogeneous signal intensity distributions in histological compartments of tumor tissue sections. The levels of tamoxifen in tumor cells compared with stroma were higher in ER-positive tissues, whereas ER-negative tissue sections showed lower signal intensities in tumor cells. CONCLUSIONS: The experimental model was successfully applied on frozen tumor samples allowing for differentiation between ER groups based on distribution of tamoxifen. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40169-016-0090-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-03-10 /pmc/articles/PMC4786513/ /pubmed/26965929 http://dx.doi.org/10.1186/s40169-016-0090-9 Text en © Végvári et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Research Végvári, Ákos Shavkunov, Alexander S. Fehniger, Thomas E. Grabau, Dorthe Niméus, Emma Marko-Varga, György Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging |
title | Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging |
title_full | Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging |
title_fullStr | Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging |
title_full_unstemmed | Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging |
title_short | Localization of tamoxifen in human breast cancer tumors by MALDI mass spectrometry imaging |
title_sort | localization of tamoxifen in human breast cancer tumors by maldi mass spectrometry imaging |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786513/ https://www.ncbi.nlm.nih.gov/pubmed/26965929 http://dx.doi.org/10.1186/s40169-016-0090-9 |
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