Publication:
1H HR-MAS NMR Based Metabolic Profiling of Cells in Response to Treatment with a Hexacationic Ruthenium Metallaprism as Potential Anticancer Drug.

cris.virtual.author-orcid0000-0001-8649-1098
cris.virtual.author-orcid0000-0003-2096-0618
cris.virtualsource.author-orcid84e9d75d-71ab-491b-8e9f-7b6422b8a3b2
cris.virtualsource.author-orciddebd1964-a7e7-4bec-a3a6-44f28036fecd
cris.virtualsource.author-orcide9401515-a542-4d08-a375-8da12fe69df6
cris.virtualsource.author-orcid3ff12425-40ac-4b25-8102-2fd226edb760
datacite.rightsopen.access
dc.contributor.authorVermathen, Martina
dc.contributor.authorPaul, Lydia E H
dc.contributor.authorDiserens, Gaëlle
dc.contributor.authorVermathen, Peter
dc.contributor.authorFurrer, Julien
dc.date.accessioned2024-10-23T18:37:12Z
dc.date.available2024-10-23T18:37:12Z
dc.date.issued2015
dc.description.abstract1H high resolution magic angle spinning (HR-MAS) NMR spectroscopy was applied in combination with multivariate statistical analyses to study the metabolic response of whole cells to the treatment with a hexacationic ruthenium metallaprism [1]6+ as potential anticancer drug. Human ovarian cancer cells (A2780), the corresponding cisplatin resistant cells (A2780cisR), and human embryonic kidney cells (HEK-293) were each incubated for 24 h and 72 h with [1]6+ and compared to untreated cells. Different responses were obtained depending on the cell type and incubation time. Most pronounced changes were found for lipids, choline containing compounds, glutamate and glutathione, nucleotide sugars, lactate, and some amino acids. Possible contributions of these metabolites to physiologic processes are discussed. The time-dependent metabolic response patterns suggest that A2780 cells on one hand and HEK-293 cells and A2780cisR cells on the other hand may follow different cell death pathways and exist in different temporal stages thereof.
dc.description.sponsorshipDIPR, Magnetresonanz-Spektroskopie und Methodologie (AMSM)
dc.description.sponsorshipDepartement für Chemie und Biochemie (DCB)
dc.identifier.doi10.7892/boris.69838
dc.identifier.pmid26024484
dc.identifier.publisherDOI10.1371/journal.pone.0128478
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/133968
dc.language.isoen
dc.publisherPublic Library of Science
dc.relation.ispartofPLoS ONE
dc.relation.issn1932-6203
dc.relation.organizationDCD5A442C14DE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BA64E17DE0405C82790C4DE2
dc.relation.schoolDCD5A442C27BE17DE0405C82790C4DE2
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.subject.ddc500 - Science::540 - Chemistry
dc.title1H HR-MAS NMR Based Metabolic Profiling of Cells in Response to Treatment with a Hexacationic Ruthenium Metallaprism as Potential Anticancer Drug.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue5
oaire.citation.startPagee0128478
oaire.citation.volume10
oairecerif.author.affiliationDepartement für Chemie und Biochemie (DCB)
oairecerif.author.affiliationDIPR, Magnetresonanz-Spektroskopie und Methodologie (AMSM)
oairecerif.author.affiliationDIPR, Magnetresonanz-Spektroskopie und Methodologie (AMSM)
oairecerif.author.affiliationDepartement für Chemie und Biochemie (DCB)
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unibe.description.ispublishedpub
unibe.eprints.legacyId69838
unibe.journal.abbrevTitlePLOS ONE
unibe.refereedtrue
unibe.subtype.articlejournal

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