Summary of Study ST003297

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 PR002048. The data can be accessed directly via it's Project DOI: 10.21228/M8WG0S This work is supported by NIH grant, U2C- DK119886.

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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 IDST003297
Study TitleMetabolomic profiling of cultured TRAMP-C2 cells in the presence or absence of PD-L1.
Study SummaryRecent evidence suggests that PD-L1, well-known as the ligand of the immune inhibitory receptor PD-1, can have cell-intrinsic effects in cancer and immune cells. One such cell-intrinsic effect is modulation of cellular metabolism, including regulation of mTOR activity and glycolysis. Here, we analyzed the metabolome of cultured mouse prostate cancer cells (TRAMP-C2) expressing PD-L1 or with PD-L1 deleted via CRISPR/Cas9.
Institute
University of Ottawa
Last NameHodgins
First NameJonathan
Address451 Smyth Rd, Ottawa, ON K1H 8M5, Canada
Emailjonathanhodgins17@gmail.com
Phone613-562-5800
Submit Date2024-05-21
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2024-07-28
Release Version1
Jonathan Hodgins Jonathan Hodgins
https://dx.doi.org/10.21228/M8WG0S
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN005401
Analysis type MS
Chromatography type Reversed phase
Chromatography system Agilent 1290 Infinity II
Column Agilent ZORBAX RRHD Extend-C18 (50 x 2.1mm,1.8um)
MS Type ESI
MS instrument type Triple quadrupole
MS instrument name Agilent 6470A
Ion Mode NEGATIVE
Units uM

MS:

MS ID:MS005128
Analysis ID:AN005401
Instrument Name:Agilent 6470A
Instrument Type:Triple quadrupole
MS Type:ESI
MS Comments:Multiple reaction monitoring (MRM) transitions were optimized using authentic standards and quality control samples. Metabolites were quantified by integrating the area under the curve of each compound using external standard calibration curves with Mass Hunter Quant (Agilent). No corrections for ion suppression or enhancement were applied.
Ion Mode:NEGATIVE
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