Summary of Study ST001903

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001198. The data can be accessed directly via it's Project DOI: http://dx.doi.org/10.21228/M8VD7F This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST001903
Study TitleEffect of ketogenic diet on the plasma and tumor metabolome of melanoma-bearing mice
Study TypeMetabolomics analysis
Study SummaryGrowing evidence supports the use of low-carbohydrate/high-fat ketogenic diets (KDs) together with standard therapies to improve cancer treatment outcomes. However, conflicting data exist regarding the efficacy of KDs in melanoma, the deadliest skin cancer. Here, we show that two different KD formulations effectively reduced tumor growth in immunocompromised mice bearing genetically and metabolically heterogeneous human melanoma xenografts. Furthermore, the KDs exerted a metastasis-reducing effect in an immunocompetent syngeneic melanoma mouse model. Ketone bodies did not directly influence melanoma cell proliferation; therefore, we performed an in-depth metabolomics analysis using the MxP® Quant 500 kit combined with a acylcarnitine assay (biocrates life sciences ag)to elucidate potential anti-tumor mechanisms in vivo. Targeted analysis of plasma and tumor metabolomes revealed distinct changes in amino acid metabolism induced by the KDs. Moreover, the KDs increased sphingomyelin synthesis and hydroxylation of certain lipids. Thus, KDs simultaneously affect multiple metabolic pathways to create an unfavorable environment for melanoma cell proliferation, supporting their potential as a complementary nutritional approach to melanoma therapy.
Institute
University Hospital of the Paracelsus Medical University Salzburg
Last NameWeber
First NameDaniela
AddressMüllner Hauptstraße 48, 5020 Salzburg, Austria
Emaild.weber@salk.at
Phone0043 57255 26274
Submit Date2021-08-10
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS/MS(Dir. Inf.)
Release Date2022-07-11
Release Version1
Daniela Weber Daniela Weber
http://dx.doi.org/10.21228/M8VD7F
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN003815 AN003816 AN003817
Analysis type MS MS MS
Chromatography type Reversed phase None (Direct infusion) Reversed phase
Chromatography system Waters Acquity Waters Acquity Thermo Dionex Ultimate 3000
Column MxP Quant 500 Kit System MxP Quant 500 Kit System Biocrates Acylcarnitine
MS Type ESI ESI ESI
MS instrument type Triple quadrupole Triple quadrupole Triple quadrupole
MS instrument name Waters TQ-S MS Waters TQ-S MS Thermo TQS Vantage
Ion Mode POSITIVE UNSPECIFIED POSITIVE
Units uM uM uM

Chromatography:

Chromatography ID:CH002822
Instrument Name:Waters Acquity
Column Name:MxP Quant 500 Kit System
Chromatography Type:Reversed phase
  
Chromatography ID:CH002823
Instrument Name:Waters Acquity
Column Name:MxP Quant 500 Kit System
Chromatography Type:None (Direct infusion)
  
Chromatography ID:CH002824
Instrument Name:Thermo Dionex Ultimate 3000
Column Name:Biocrates Acylcarnitine
Chromatography Type:Reversed phase
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