Summary of Study ST003532

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 PR002173. The data can be accessed directly via it's Project DOI: 10.21228/M8R23J 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 IDST003532
Study TitleMicropeptide hSPAR, a glutamine regulator, suppresses tumor growth via TRIM21-P27KIP1-mTOR pathway - HEK293T human embryonic kidney cells
Study SummaryThe microprotein hSPAR can specifically regulate the mTOR signaling activity and cell proliferation in breast cancer cells. However, such regulatory effects of hSPAR are not applicable in HEK293T cells. Metabolic data of amino acids indicate that overexpressing hSPAR does not affect the content of amino acids in HEK293T cells, including glutamine. The metabolic variations in amino acids triggered by hSPAR in different cell types may be the underlying molecular mechanism for the distinct regulatory effects of hSPAR.
Institute
University Of Science And Technology of China
Last NameWang
First NameWei
Address443 Huangshan Road, Hefei city, Anhui Province, 230022, China
EmailWW571@mail.ustc.edu.cn
Phone18604523231
Submit Date2024-10-10
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2025-01-06
Release Version1
Wei Wang Wei Wang
https://dx.doi.org/10.21228/M8R23J
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Collection:

Collection ID:CO003654
Collection Summary:The HEK293T human embryonic kidney cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) , containing 10% fetal bovine serum and 1% penicillin-streptomycin under humidified atmosphere of 5% CO2 at 37°C.Ce11s were counted, washed with cold PBS and then flash-frozen in liquid N2.
Sample Type:Epithelial cells
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