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Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs

The study of cell lines by nuclear magnetic resonance (NMR) spectroscopy metabolomics represents a powerful tool to understand how the local metabolism and biochemical pathways are influenced by external or internal stimuli. In particular, the use of adherent mammalian cells is emerging in the metab...

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Autores principales: Lauri, Ilaria, Savorani, Francesco, Iaccarino, Nunzia, Zizza, Pasquale, Pavone, Luigi Michele, Novellino, Ettore, Engelsen, Søren Balling, Randazzo, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812333/
https://www.ncbi.nlm.nih.gov/pubmed/26784246
http://dx.doi.org/10.3390/metabo6010004
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author Lauri, Ilaria
Savorani, Francesco
Iaccarino, Nunzia
Zizza, Pasquale
Pavone, Luigi Michele
Novellino, Ettore
Engelsen, Søren Balling
Randazzo, Antonio
author_facet Lauri, Ilaria
Savorani, Francesco
Iaccarino, Nunzia
Zizza, Pasquale
Pavone, Luigi Michele
Novellino, Ettore
Engelsen, Søren Balling
Randazzo, Antonio
author_sort Lauri, Ilaria
collection PubMed
description The study of cell lines by nuclear magnetic resonance (NMR) spectroscopy metabolomics represents a powerful tool to understand how the local metabolism and biochemical pathways are influenced by external or internal stimuli. In particular, the use of adherent mammalian cells is emerging in the metabolomics field in order to understand the molecular mechanism of disease progression or, for example, the cellular response to drug treatments. Hereto metabolomics investigations for this kind of cells have generally been limited to mass spectrometry studies. This study proposes an optimized protocol for the analysis of the endo-metabolome of human colon cancer cells (HCT116) by NMR. The protocol includes experimental conditions such as washing, quenching and extraction. In order to test the proposed protocol, it was applied to an exploratory study of cancer cells with and without treatment by anti-cancer drugs, such as DNA G-quadruplex binders and Adriamycin (a traditional anti-cancer drug). The exploratory NMR metabolomics analysis resulted in NMR assignment of all endo-metabolites that could be detected and provided preliminary insights about the biological behavior of the drugs tested.
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spelling pubmed-48123332016-04-06 Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs Lauri, Ilaria Savorani, Francesco Iaccarino, Nunzia Zizza, Pasquale Pavone, Luigi Michele Novellino, Ettore Engelsen, Søren Balling Randazzo, Antonio Metabolites Article The study of cell lines by nuclear magnetic resonance (NMR) spectroscopy metabolomics represents a powerful tool to understand how the local metabolism and biochemical pathways are influenced by external or internal stimuli. In particular, the use of adherent mammalian cells is emerging in the metabolomics field in order to understand the molecular mechanism of disease progression or, for example, the cellular response to drug treatments. Hereto metabolomics investigations for this kind of cells have generally been limited to mass spectrometry studies. This study proposes an optimized protocol for the analysis of the endo-metabolome of human colon cancer cells (HCT116) by NMR. The protocol includes experimental conditions such as washing, quenching and extraction. In order to test the proposed protocol, it was applied to an exploratory study of cancer cells with and without treatment by anti-cancer drugs, such as DNA G-quadruplex binders and Adriamycin (a traditional anti-cancer drug). The exploratory NMR metabolomics analysis resulted in NMR assignment of all endo-metabolites that could be detected and provided preliminary insights about the biological behavior of the drugs tested. MDPI 2016-01-15 /pmc/articles/PMC4812333/ /pubmed/26784246 http://dx.doi.org/10.3390/metabo6010004 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lauri, Ilaria
Savorani, Francesco
Iaccarino, Nunzia
Zizza, Pasquale
Pavone, Luigi Michele
Novellino, Ettore
Engelsen, Søren Balling
Randazzo, Antonio
Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs
title Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs
title_full Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs
title_fullStr Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs
title_full_unstemmed Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs
title_short Development of an Optimized Protocol for NMR Metabolomics Studies of Human Colon Cancer Cell Lines and First Insight from Testing of the Protocol Using DNA G-Quadruplex Ligands as Novel Anti-Cancer Drugs
title_sort development of an optimized protocol for nmr metabolomics studies of human colon cancer cell lines and first insight from testing of the protocol using dna g-quadruplex ligands as novel anti-cancer drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812333/
https://www.ncbi.nlm.nih.gov/pubmed/26784246
http://dx.doi.org/10.3390/metabo6010004
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