Summary of Study ST003060

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 PR001906. The data can be accessed directly via it's Project DOI: 10.21228/M8BQ6H 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 IDST003060
Study TitleFluxomics of hormone deprivation in ER+ breast cancer cell lines
Study TypeFluxomics
Study SummaryDespite adjuvant treatment with endocrine therapies, estrogen receptor-positive (ER+) breast cancers recur in a significant proportion of patients. Recurrences are attributable to clinically undetectable endocrine-tolerant persister cancer cells that retain tumor-forming potential. We observed that persistence occurred stochastically without genetic predisposition. Genome-wide screening in persisters revealed a survival mechanism involving metabolic reprogramming with reliance upon mitochondrial respiration. Proteomic profiling showed reduced levels of glycolytic proteins in persisters. Metabolic tracing of glucose revealed an energy-depleted state in persisters where oxidative phosphorylation was required to generate ATP. Persisters exhibiting residual proliferation in human breast tumors following neoadjuvant endocrine therapy showed increased mitochondrial content. Pharmacological inhibition of oxidative phosphorylation suppressed the tumor-forming potential of persisters and synergized with the anti-estrogen fulvestrant to induce regression of patient-derived xenografts, supporting therapeutic targeting of mitochondrial metabolism to help eradicate residual disease.
Institute
Dartmouth College
DepartmentMolecular and Systems Biology
LaboratoryMiller
Last NameMiller
First NameTodd
AddressHanover, NH
EmailTodd.W.Miller@Dartmouth.edu
Phone603-646-5507
Submit Date2024-01-15
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2024-02-14
Release Version1
Todd Miller Todd Miller
https://dx.doi.org/10.21228/M8BQ6H
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001906
Project DOI:doi: 10.21228/M8BQ6H
Project Title:Investigation of metabolism in ER+ breast cancer
Project Type:MS
Project Summary:This study aims to observe alterations in substrate preference in ER+ breast cancer cell lines when subjected to endocrine therapy
Institute:University of Michigan
Department:MRC2
Laboratory:BRCF metabolomics core
Last Name:Kachman
First Name:Maureen
Address:Ann Arbor, MI, USA
Email:mkachman@med.umich.edu
Phone:734-232-0842

Subject:

Subject ID:SU003175
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

Factors:

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

mb_sample_id local_sample_id 13C label Hormone treatment
SA331845BlankBlank Blank
SA331847MCF7 HD glucose non-labeled controlglucose No
SA331848MCF7 HD glucose_3glucose No
SA331849MCF7 HD glucose_1glucose No
SA331850MCF7 HD glucose_2glucose No
SA331851MCF7 E2 glucose_2glucose Yes
SA331852MCF7 E2 glucose_1glucose Yes
SA331853MCF7 E2 glucose_3glucose Yes
SA331854MCF7 E2 glucose non-labeled controlglucose Yes
SA331855MCF7 HD oleic acid non-labeled controloleic acid No
SA331856MCF7 HD oleic acid_1oleic acid No
SA331857MCF7 HD oleic acid_3oleic acid No
SA331858MCF7 HD oleic acid_2oleic acid No
SA331859MCF7 E2 oleic acid_1oleic acid Yes
SA331860MCF7 E2 oleic acid_2oleic acid Yes
SA331861MCF7 E2 oleic acid_3oleic acid Yes
SA331862MCF7 E2 oleic acid non-labeled controloleic acid Yes
SA331846PoolPool Pool
Showing results 1 to 18 of 18

Collection:

Collection ID:CO003168
Collection Summary:Cells were washed with 150 mM ammonium acetate and flash frozen, before storage at -80deg C.
Sample Type:Breast cancer cells

Treatment:

Treatment ID:TR003184
Treatment Summary:Cells are hormone deprived for 21 days, before reseeding into 10 cm dishes at 3-5e6 cells/dish. After 2 days of allowing the cells to properly adhere, cells were labeled with 4.5 g/L 13C-glucose or 100 uM 13C-oleic acid according to the sample preparation guidelines.

Sample Preparation:

Sampleprep ID:SP003181
Sampleprep Summary:Glycolysis-TCA (GlyTCA) by Ion Pairing UPLC-QTOF mass spectrometry
Sampleprep Protocol Filename:GlyTCA_SOP_QTOF-with-prep-V1_20240118.pdf

Combined analysis:

Analysis ID AN005015
Analysis type MS
Chromatography type Ion pair
Chromatography system Agilent 1290 Infinity II
Column Agilent ZORBAX RRHD Extend-C18 (150 x 2.1mm, 1.8um, 80Å)
MS Type ESI
MS instrument type QTOF
MS instrument name Agilent 6545 QTOF
Ion Mode NEGATIVE
Units counts

Chromatography:

Chromatography ID:CH003788
Chromatography Summary:Ion Pairing UPLC
Instrument Name:Agilent 1290 Infinity II
Column Name:Agilent ZORBAX RRHD Extend-C18 (150 x 2.1mm, 1.8um, 80Å)
Column Temperature:35
Flow Gradient:(Time PercentA PercentB PercentC Flow) (2 100 0 0 0.25) (12 1 99 0 0.25) (19.5 1 99 0 0.25) (20 5 0 95 0.5) (21 5 0 95 0.8) (22 5 0 95 0.8) (26 5 0 95 0.6) (26.1 5 0 95 0.4) (26.2 100 0 0 0.4) (31.8 100 0 0 0.25) (32 100 0 0 0.25)
Flow Rate:0.25 ml/min
Solvent A:97% water, 3% methanol, 5mM tributylamine, 5.5mM acetic acid, 12.5nM medronic acid
Solvent B:100% methanol, 5mM tributylamine, 5.5mM acetic acid, 12.5nM medronic acid
Chromatography Type:Ion pair
Solvent C:100% Acetonitrile

MS:

MS ID:MS004754
Analysis ID:AN005015
Instrument Name:Agilent 6545 QTOF
Instrument Type:QTOF
MS Type:ESI
MS Comments:All data acquisition and processing done using vendor software (Agilent)
Ion Mode:NEGATIVE
Acquisition Parameters File:M001_30min_profile_MS1_10ul_WBsensON_AcqMethodReport.pdf
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