Summary of Study ST001920

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 PR001211. The data can be accessed directly via it's Project DOI: 10.21228/M85Q6Z 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.

Perform statistical analysis  |  Show all samples  |  Show named metabolites  |  Download named metabolite data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST001920
Study TitleMetabolic and lipidomic characterization of radioresistant MDA-MB-231 human breast cancer cells to investigate potential therapeutic targets
Study SummaryTo provide preliminary insights into metabolic and lipidomic characteristics in radioresistant triple-negative breast cancer (TNBC) cells and suggest potential therapeutic targets, we performed a comprehensive metabolic and lipidomic profiling of radioresistant MDA-MB-231 (MDA-MB-231/RR) TNBC cells and their parental cells using gas chromatography-mass spectrometry and nano electrospray ionization-mass spectrometry, followed by multivariate statistical analysis. Buthionine sulfoximine (BSO) and radiation were co-treated to radioresistant TNBC cells. The level of glutathione (GSH) was significantly increased, and the levels of GSH synthesis-related metabolites, such as cysteine, glycine, and glutamine were also increased in MDA-MB-231/RR cells. In contrast, the level of lactic acid was significantly reduced. In addition, reactive oxygen species (ROS) level was decreased in MDA-MB-231/RR cells. In the lipidomic profiles of MDA-MB-231/RR cells, the levels of phosphatidylcholine (PC) and phosphatidylethanolamine (PE) were significantly increased, whereas those of most of the phosphatidylinositol species were significantly decreased. BSO sensitized MDA-MB-231/RR cells to radiotherapy, which resulted in decreased GSH level and increased ROS level and apoptosis. Radioresistant TNBC cells showed distinct metabolic and lipidomic characteristics compared to their parental cells. We suggested activated GSH, PC, and PE biosynthesis pathways as potential targets for treating radioresistant TNBC cells. Particularly, enhanced radiosensitivity was achieved by inhibition of GSH biosynthesis in MDA-MB-231/RR cells.
Institute
ChungAng University
DepartmentCollege of Pharmacy
LaboratoryNatural product biotechnology and Metabolomics
Last NameLee
First NameHwanhui
AddressCollege of Pharmacy, Chung-Ang University, Seoul 06974, Republic of Korea
Emailhwanhui56@gmail.com
Phone+8228205605
Submit Date2021-09-22
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo), d
Analysis Type DetailGC-MS/MS(Dir. inf.)
Release Date2021-10-02
Release Version1
Hwanhui Lee Hwanhui Lee
https://dx.doi.org/10.21228/M85Q6Z
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Combined analysis:

Analysis ID AN003119 AN003120 AN003121
Analysis type MS MS MS
Chromatography type GC None (Direct infusion) None (Direct infusion)
Chromatography system Agilent 7890A automated nanoinfusion/nanospray source automated nanoinfusion/nanospray source
Column Agilent DB5-MS (30m x 0.25mm, 0.25um) None None
MS Type EI ESI ESI
MS instrument type Triple axis detector Ion trap Ion trap
MS instrument name Agilent 5975C Thermo LTQ XL Thermo LTQ XL
Ion Mode POSITIVE POSITIVE NEGATIVE
Units relative intensity/µg proteins relative intensity/µg proteins relative intensity/µg proteins

MS:

MS ID:MS002900
Analysis ID:AN003119
Instrument Name:Agilent 5975C
Instrument Type:Triple axis detector
MS Type:EI
MS Comments:The initial oven temperature was set at 70 °C and then increased to 190°C (5 °C/min), 240 °C (6 °C/min), and 280 °C (5 °C/min). Data was processed using Expressionist® MSX software (version 2013.0.39, Genedata, Basel, Switzerland).
Ion Mode:POSITIVE
  
MS ID:MS002901
Analysis ID:AN003120
Instrument Name:Thermo LTQ XL
Instrument Type:Ion trap
MS Type:ESI
MS Comments:The raw data files (*.raw) were transformed to *.mzXML using the ProteoWizard MSConvert. Data was processed using Expressionist® MSX software (version 2013.0.39, Genedata, Basel, Switzerland).
Ion Mode:POSITIVE
Capillary Temperature:200 °C
Capillary Voltage:20 V
Gas Pressure:0.4 psi
Ion Spray Voltage:1.4 kV
  
MS ID:MS002902
Analysis ID:AN003121
Instrument Name:Thermo LTQ XL
Instrument Type:Ion trap
MS Type:ESI
MS Comments:The raw data files (*.raw) were transformed to *.mzXML using the ProteoWizard MSConvert. Data was processed using Expressionist® MSX software (version 2013.0.39, Genedata, Basel, Switzerland).
Ion Mode:NEGATIVE
Capillary Temperature:200 °C
Capillary Voltage:−2 V
Gas Pressure:0.6 psi
Ion Spray Voltage:1.7 kV
  logo