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Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines.
The lipid composition of five human breast cancer cell lines (MCF-7, T47D, ZR-75-1, SKBR3 and MDA-MB231) was assessed by proton magnetic resonance spectroscopy (MRS) in whole cells and membrane-enriched fractions. The proportions of the three main lipid resonances in 1D spectra were different for ea...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977411/ https://www.ncbi.nlm.nih.gov/pubmed/1329906 |
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author | Le Moyec, L. Tatoud, R. Eugène, M. Gauvillé, C. Primot, I. Charlemagne, D. Calvo, F. |
author_facet | Le Moyec, L. Tatoud, R. Eugène, M. Gauvillé, C. Primot, I. Charlemagne, D. Calvo, F. |
author_sort | Le Moyec, L. |
collection | PubMed |
description | The lipid composition of five human breast cancer cell lines (MCF-7, T47D, ZR-75-1, SKBR3 and MDA-MB231) was assessed by proton magnetic resonance spectroscopy (MRS) in whole cells and membrane-enriched fractions. The proportions of the three main lipid resonances in 1D spectra were different for each cell line. These resonances included mobile methyl and methylene functions from fatty acids of triglycerides and phospholipids and N-trimethyl from choline of phospholipids. T47D and ZR-75-1 cells presented a high methylene/methyl ratio (6.02 +/- 0.35 and 6.28 +/- 0.90). This ratio was significantly lower for SKBR3, MCF-7 and MDA-MB231 cells (2.76 +/- 0.22, 2.27 +/- 0.57 and 1.39 +/- 0.39). The N-trimethyl/methyl ratio was high for MDA-MB231 and SKBR3 cells (1.38 +/- 0.54 and 0.86 +/- 0.32), but lower for MCF-7, T47D and ZR-75-1 cells (0.49 +/- 0.11, 0.16 +/- 0.07 and 0.07 +/- 0.03). 2D COSY spectra confirmed these different proportions in mobile lipids. From 1D spectra obtained on membrane preparations, T47D and ZR-75-1 were the only cell lines to retain a signal from mobile methylene functions. These differences might be related to the heterogeneity found for several parameters of these cells (tumorigenicity, growth rate, hormone receptors); an extended number of cases from fresh samples might enable clinical correlations. |
format | Text |
id | pubmed-1977411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19774112009-09-10 Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. Le Moyec, L. Tatoud, R. Eugène, M. Gauvillé, C. Primot, I. Charlemagne, D. Calvo, F. Br J Cancer Research Article The lipid composition of five human breast cancer cell lines (MCF-7, T47D, ZR-75-1, SKBR3 and MDA-MB231) was assessed by proton magnetic resonance spectroscopy (MRS) in whole cells and membrane-enriched fractions. The proportions of the three main lipid resonances in 1D spectra were different for each cell line. These resonances included mobile methyl and methylene functions from fatty acids of triglycerides and phospholipids and N-trimethyl from choline of phospholipids. T47D and ZR-75-1 cells presented a high methylene/methyl ratio (6.02 +/- 0.35 and 6.28 +/- 0.90). This ratio was significantly lower for SKBR3, MCF-7 and MDA-MB231 cells (2.76 +/- 0.22, 2.27 +/- 0.57 and 1.39 +/- 0.39). The N-trimethyl/methyl ratio was high for MDA-MB231 and SKBR3 cells (1.38 +/- 0.54 and 0.86 +/- 0.32), but lower for MCF-7, T47D and ZR-75-1 cells (0.49 +/- 0.11, 0.16 +/- 0.07 and 0.07 +/- 0.03). 2D COSY spectra confirmed these different proportions in mobile lipids. From 1D spectra obtained on membrane preparations, T47D and ZR-75-1 were the only cell lines to retain a signal from mobile methylene functions. These differences might be related to the heterogeneity found for several parameters of these cells (tumorigenicity, growth rate, hormone receptors); an extended number of cases from fresh samples might enable clinical correlations. Nature Publishing Group 1992-10 /pmc/articles/PMC1977411/ /pubmed/1329906 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 Le Moyec, L. Tatoud, R. Eugène, M. Gauvillé, C. Primot, I. Charlemagne, D. Calvo, F. Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. |
title | Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. |
title_full | Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. |
title_fullStr | Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. |
title_full_unstemmed | Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. |
title_short | Cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. |
title_sort | cell and membrane lipid analysis by proton magnetic resonance spectroscopy in five breast cancer cell lines. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977411/ https://www.ncbi.nlm.nih.gov/pubmed/1329906 |
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