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Metabolic Profiling of Cells in Response to Drug Treatment using 1 H High-resolution Magic Angle Spinning (HR-MAS) NMR Spectroscopy.
- Source :
-
Chimia [Chimia (Aarau)] 2017 Mar 29; Vol. 71 (3), pp. 124-129. - Publication Year :
- 2017
-
Abstract
- High-resolution magic angle spinning (HR-MAS) is an NMR technique that provides access to well resolved liquid-like 1H NMR spectra of semi-solid samples. Therefore, 1H HR-MAS NMR spectroscopy has become an important tool for the direct analysis of biological samples such as tissues and cells in a mostly non-destructive way. Here, we focus on the application of HR-MAS NMR combined with multivariate statistical methods used for metabolic profiling of cells and in particular for the study of cellular metabolic responses to drug exposure. The principles of HR-MAS and the metabolomic approach are briefly described. As an example, a study on the metabolic response of different cell types towards treatment with a highly cytotoxic hexacationic ruthenium metallaprism as potential anti-cancer drug is presented. Specific metabolites and metabolic pathways are suggested to be associated with the cellular response. The study demonstrates the potential of HR-MAS metabolomics applied to cells for addressing the intracellular processes involved in the treatment with organometallic drugs.
- Subjects :
- Amino Acids analysis
Antineoplastic Agents chemistry
Antineoplastic Agents pharmacology
Cell Line, Tumor
Cisplatin pharmacology
Coordination Complexes chemistry
Drug Resistance, Neoplasm drug effects
HEK293 Cells
Humans
Magnetic Resonance Spectroscopy instrumentation
Metabolomics instrumentation
Neoplasms drug therapy
Neoplasms metabolism
Neoplasms pathology
Principal Component Analysis
Ruthenium chemistry
Coordination Complexes pharmacology
Magnetic Resonance Spectroscopy methods
Metabolomics methods
Subjects
Details
- Language :
- English
- ISSN :
- 0009-4293
- Volume :
- 71
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Chimia
- Publication Type :
- Academic Journal
- Accession number :
- 28351458
- Full Text :
- https://doi.org/10.2533/chimia.2017.124