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dc.contributor.authorAndersen, Maria Karoline
dc.contributor.authorHøiem, Therese Stork
dc.contributor.authorClaes, Britt S.R.
dc.contributor.authorBalluff, Benjamin
dc.contributor.authorMarta, Martin-Lorenzo
dc.contributor.authorRichardsen, Elin
dc.contributor.authorKrossa, Sebastian
dc.contributor.authorBertilsson, Helena
dc.contributor.authorHeeren, Ron M.A.
dc.contributor.authorRye, Morten Beck
dc.contributor.authorGiskeødegård, Guro F.
dc.contributor.authorBathen, Tone Frost
dc.contributor.authorTessem, May-Britt
dc.date.accessioned2021-04-30T09:25:19Z
dc.date.available2021-04-30T09:25:19Z
dc.date.created2021-02-01T13:16:51Z
dc.date.issued2021
dc.identifier.citationCancer & Metabolism. 2021, .en_US
dc.identifier.issn2049-3002
dc.identifier.urihttps://hdl.handle.net/11250/2740542
dc.description.abstractBackground Prostate cancer tissues are inherently heterogeneous, which presents a challenge for metabolic profiling using traditional bulk analysis methods that produce an averaged profile. The aim of this study was therefore to spatially detect metabolites and lipids on prostate tissue sections by using mass spectrometry imaging (MSI), a method that facilitates molecular imaging of heterogeneous tissue sections, which can subsequently be related to the histology of the same section. Methods Here, we simultaneously obtained metabolic and lipidomic profiles in different prostate tissue types using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) MSI. Both positive and negative ion mode were applied to analyze consecutive sections from 45 fresh-frozen human prostate tissue samples (N = 15 patients). Mass identification was performed with tandem MS. Results Pairwise comparisons of cancer, non-cancer epithelium, and stroma revealed several metabolic differences between the tissue types. We detected increased levels of metabolites crucial for lipid metabolism in cancer, including metabolites involved in the carnitine shuttle, which facilitates fatty acid oxidation, and building blocks needed for lipid synthesis. Metabolites associated with healthy prostate functions, including citrate, aspartate, zinc, and spermine had lower levels in cancer compared to non-cancer epithelium. Profiling of stroma revealed higher levels of important energy metabolites, such as ADP, ATP, and glucose, and higher levels of the antioxidant taurine compared to cancer and non-cancer epithelium. Conclusions This study shows that specific tissue compartments within prostate cancer samples have distinct metabolic profiles and pinpoint the advantage of methodology providing spatial information compared to bulk analysis. We identified several differential metabolites and lipids that have potential to be developed further as diagnostic and prognostic biomarkers for prostate cancer. Spatial and rapid detection of cancer-related analytes showcases MALDI-TOF MSI as a promising and innovative diagnostic tool for the clinic.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleSpatial differentiation of metabolism in prostate cancer tissue by MALDI-TOF MSIen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber13en_US
dc.source.journalCancer & Metabolismen_US
dc.identifier.doihttps://doi.org/10.1186/s40170-021-00242-z
dc.identifier.cristin1885033
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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