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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Collection:

Collection ID:CO003411
Collection Summary:Cells were placed on ice and the culture media was removed. Cells were washed twice with ice-cold PBS, and scraped into chilled 2 mL tubes, and frozen until metabolite extraction.
Sample Type:Cultured cells
Storage Conditions:-80℃
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