Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Le Moyec, L., Tatoud, R., Eugène, M., Gauvillé, C., Primot, I., Charlemagne, D., Calvo, F.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977411/
https://www.ncbi.nlm.nih.gov/pubmed/1329906
_version_ 1782135255980834816
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
work_keys_str_mv AT lemoyecl cellandmembranelipidanalysisbyprotonmagneticresonancespectroscopyinfivebreastcancercelllines
AT tatoudr cellandmembranelipidanalysisbyprotonmagneticresonancespectroscopyinfivebreastcancercelllines
AT eugenem cellandmembranelipidanalysisbyprotonmagneticresonancespectroscopyinfivebreastcancercelllines
AT gauvillec cellandmembranelipidanalysisbyprotonmagneticresonancespectroscopyinfivebreastcancercelllines
AT primoti cellandmembranelipidanalysisbyprotonmagneticresonancespectroscopyinfivebreastcancercelllines
AT charlemagned cellandmembranelipidanalysisbyprotonmagneticresonancespectroscopyinfivebreastcancercelllines
AT calvof cellandmembranelipidanalysisbyprotonmagneticresonancespectroscopyinfivebreastcancercelllines