Summary of Study ST002839

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 PR001778. The data can be accessed directly via it's Project DOI: 10.21228/M8WB1S 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 IDST002839
Study TitleMetabolic alteration during ferroptotic process in cancer cells.
Study SummaryTargeting ferroptosis, an iron-dependent form of regulated cell death triggered by the lethal overload of lipid peroxides, in cancer therapy is impeded by our limited understanding of the intersection of tumour’s metabolic feature and ferroptosis vulnerability. In this study, we performed metabolomics in cancer cell lines pretreated with ferroptosis inducer RSL3 and control DMSO. We noted that the levels of a series of metabolites were significantly impacted by the RSL3 treatment, such as upregulated polyamines including putrescine, spermidine, and spermine. According to our previous study, we proved the pro-ferroptotic feature of polyamines in tumor cells, which was derived from the H2O2 produced during the polyamine metabolic process. This finding is consistent with our RNA-Seq data indicating upregulated ODC1 in the ferroptotic process. Therefore, it could be speculated that the RSL3-induced polyamine production leads to a positive-feedback loop that amplifies ferroptosis in tumor cells.
Institute
Zhongshan Hospital Fudan University
Last NameBi
First NameGuoshu
AddressZhongshan Hospital, Fudan University, No. 180, Fenglin Road, Xuhui District, Shanghai, China
Email18211210035@fudan.edu.cn
Phone86 64041990
Submit Date2023-08-25
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2023-09-07
Release Version1
Guoshu Bi Guoshu Bi
https://dx.doi.org/10.21228/M8WB1S
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001778
Project DOI:doi: 10.21228/M8WB1S
Project Title:Metabolites alteration during ferroptotic process in tumor cells
Project Summary:Targeting ferroptosis, an iron-dependent form of regulated cell death triggered by the lethal overload of lipid peroxides, in cancer therapy is impeded by our limited understanding of the intersection of tumour’s metabolic feature and ferroptosis vulnerability. In the presented study, we performed metabolomics for cancer cell lines treated by ferroptosis inducer RSL3 or control DMSO.
Institute:Zhongshan Hospital Fudan University
Last Name:Bi
First Name:Guoshu
Address:Zhongshan Hospital, Fudan University, No. 180, Fenglin Road, Xuhui District, Shanghai, China
Email:18211210035@fudan.edu.cn
Phone:86 64041990

Subject:

Subject ID:SU002949
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606
Species Group:Mammals

Factors:

Subject type: Cultured cells; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA307469ND1Control
SA307470ND2Control
SA307471NR1RSL3
SA307472NR2RSL3
Showing results 1 to 4 of 4

Collection:

Collection ID:CO002942
Collection Summary:For cell samples, after being washed with ice-cold PBS, the cells were collected using a cell scraper and centrifuged for 5 min at 1,000 g. The samples were homogenized in liquid N2 for 1 min and defrosted in 4°C.
Sample Type:Tumor cells

Treatment:

Treatment ID:TR002958
Treatment Summary:A549 cells cultured in DMEM medium were treated with 0.5 uM RSL3 or DMSO for 24 h.

Sample Preparation:

Sampleprep ID:SP002955
Sampleprep Summary:After homogenization in liquid N2, 200 μL 80% methyl alcohol was added, followed by vortex for 1 min, sonication for 30 min at 4°C, and stand for 1 h at -20°C. Then, the samples were centrifuged at 12,000 rpm for 15 min at 4°C, and the supernatant was collected for subsequent LC-MS analysis.

Combined analysis:

Analysis ID AN004645 AN004646
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Waters Acquity Waters Acquity
Column Waters ACQUITY UPLC HSS T3 (100 x 2.1mm,1.8um) Waters ACQUITY UPLC HSS T3 (100 x 2.1mm,1.8um)
MS Type ESI ESI
MS instrument type Orbitrap Orbitrap
MS instrument name Thermo Q Exactive Orbitrap Thermo Q Exactive Orbitrap
Ion Mode POSITIVE NEGATIVE
Units pmol/l pmol/l

Chromatography:

Chromatography ID:CH003496
Instrument Name:Waters Acquity
Column Name:Waters ACQUITY UPLC HSS T3 (100 x 2.1mm,1.8um)
Column Temperature:45
Flow Gradient:Time:(0.01-2-4-8-10-14-15-15.1-16); Solvent A%: (95-95-70-50-20-0-0-95-95);Solvent B%: (5-5-30-50-80-100-100-5-5)
Flow Rate:0.35 mL/min
Solvent A:Water containing 0.1% methanoic acid
Solvent B:Acetonitrile containing 0.1% methanoic acid
Chromatography Type:Reversed phase

MS:

MS ID:MS004392
Analysis ID:AN004645
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:Mass Scan Range 100-1200 Resolution (full scan) 70000 Resolution (HCD MS/MS scans) 17500 Spray Voltage (V) 3800 Sheath Gas Flow Rate (Arb) 35 Aux Gas Flow Rate (Arb) 8 Capillary Temperature (°C) 320
Ion Mode:POSITIVE
  
MS ID:MS004393
Analysis ID:AN004646
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:Mass Scan Range 100-1200 Resolution (full scan) 70000 Resolution (HCD MS/MS scans) 17500 Spray Voltage (V) -3000 Sheath Gas Flow Rate (Arb) 35 Aux Gas Flow Rate (Arb) 8 Capillary Temperature (°C) 320
Ion Mode:NEGATIVE
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