Summary of Study ST001941
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 PR001229. The data can be accessed directly via it's Project DOI: 10.21228/M8V98S 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.
Study ID | ST001941 |
Study Title | Untargeted metabolomics of breast cell lines in the presence or the absence of CtBP inhibitors |
Study Summary | Experiments to test the effect of CtBP2 inhibition on metabolism of breast cell lines. In particular, experiment 1 involves comparison between a normal breast cell line (MCF102A) and a triple-negative breast cancer cell line (MDA-MB231). Experiment 2 is a study between MDA-MB231 silenced for CtBP2 by stable RNA interference (shCtBP2 cells) compared to scramble (shCTRL cells). Experiment 3 is a comparison between a normal breast cell line (MCF102A) and a triple-negative breast cancer cell line (MDA-MB231)in the presence of the absence of small-molecule CtBP inhibitors: HIPP (400 μM) or P4 (300 μM)for 48 hours. |
Institute | University of Milano-Bicocca |
Last Name | Bonanomi |
First Name | Marcella |
Address | Piazza della Scienza 4 |
marcella.bonanomi@unimib.it | |
Phone | +390264483343 |
Submit Date | 2021-08-31 |
Raw Data Available | Yes |
Raw Data File Type(s) | mzdata.xml |
Analysis Type Detail | LC-MS |
Release Date | 2021-11-04 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR001229 |
Project DOI: | doi: 10.21228/M8V98S |
Project Title: | Untargeted metabolomics of breast cell lines in the presence or the absence of CtBP inhibitors |
Project Summary: | Experiments to test the effect of CtBP2 inhibition on metabolism of breast cell lines |
Institute: | University of Milano-Bicocca |
Last Name: | Bonanomi |
First Name: | Marcella |
Address: | Piazza della Scienza 4, Milan, MI, 20126, Italy |
Email: | marcella.bonanomi@unimib.it |
Phone: | +390264483343 |
Subject:
Subject ID: | SU002019 |
Subject Type: | Cultured cells |
Subject Species: | Homo sapiens |
Taxonomy ID: | 9606 |
Factors:
Subject type: Cultured cells; Subject species: Homo sapiens (Factor headings shown in green)
mb_sample_id | local_sample_id | CELL LINE | TREATMENT |
---|---|---|---|
SA183255 | 10A CTRL 1_001 | MCF102A | CONTROL |
SA183256 | 10A CTRL 1_1 | MCF102A | CONTROL |
SA183257 | 10A CTRL 1_3 | MCF102A | CONTROL |
SA183258 | 10A CTRL 2_1 | MCF102A | CONTROL |
SA183259 | 10A CTRL 2_2 | MCF102A | CONTROL |
SA183260 | 10A CTRL 1_2 | MCF102A | CONTROL |
SA183261 | 10A CTRL 2_3 | MCF102A | CONTROL |
SA183262 | 10A CTRL 1_003 | MCF102A | CONTROL |
SA183263 | 10A CTRL 2_001 | MCF102A | CONTROL |
SA183264 | 10A CTRL 2_002 | MCF102A | CONTROL |
SA183265 | 10A CTRL 2_003 | MCF102A | CONTROL |
SA183266 | 10A CTRL 1_002 | MCF102A | CONTROL |
SA183267 | 10A HIPP 2_2 | MCF102A | HIPP |
SA183268 | 10A HIPP 2_3 | MCF102A | HIPP |
SA183269 | 10A HIPP 1_3 | MCF102A | HIPP |
SA183270 | 10A HIPP 1_2 | MCF102A | HIPP |
SA183271 | 10A HIPP 1_1 | MCF102A | HIPP |
SA183272 | 10A HIPP 2_1 | MCF102A | HIPP |
SA183273 | 10A P4 2_2 | MCF102A | P4 |
SA183274 | 10A P4 1_2 | MCF102A | P4 |
SA183275 | 10A P4 2_1 | MCF102A | P4 |
SA183276 | 10A P4 1_3 | MCF102A | P4 |
SA183277 | 10A P4 1_1 | MCF102A | P4 |
SA183278 | 10A P4 2_3 | MCF102A | P4 |
SA183279 | 231 CTRL 1_3 | MDA-MB231 | CONTROL |
SA183280 | 231 CTRL 1_001 | MDA-MB231 | CONTROL |
SA183281 | 231 CTRL 2_3 | MDA-MB231 | CONTROL |
SA183282 | 231 CTRL 2_2 | MDA-MB231 | CONTROL |
SA183283 | 231 CTRL 2_1 | MDA-MB231 | CONTROL |
SA183284 | 231 CTRL 1_2 | MDA-MB231 | CONTROL |
SA183285 | 231 CTRL 1_1 | MDA-MB231 | CONTROL |
SA183286 | 231 CTRL 2_003 | MDA-MB231 | CONTROL |
SA183287 | 231 CTRL 1_002 | MDA-MB231 | CONTROL |
SA183288 | 231 CTRL 2_002 | MDA-MB231 | CONTROL |
SA183289 | 231 CTRL 1_003 | MDA-MB231 | CONTROL |
SA183290 | 231 CTRL 2_001 | MDA-MB231 | CONTROL |
SA183291 | 231 HIPP 1_3 | MDA-MB231 | HIPP |
SA183292 | 231 HIPP 2_1 | MDA-MB231 | HIPP |
SA183293 | 231 HIPP 2_3 | MDA-MB231 | HIPP |
SA183294 | 231 HIPP 1_1 | MDA-MB231 | HIPP |
SA183295 | 231 HIPP 2_2 | MDA-MB231 | HIPP |
SA183296 | 231 HIPP 1_2 | MDA-MB231 | HIPP |
SA183297 | 231 P4 1_3 | MDA-MB231 | P4 |
SA183298 | 231 P4 2_1 | MDA-MB231 | P4 |
SA183299 | 231 P4 2_2 | MDA-MB231 | P4 |
SA183300 | 231 P4 2_3 | MDA-MB231 | P4 |
SA183301 | 231 P4 1_2 | MDA-MB231 | P4 |
SA183302 | 231 P4 1_1 | MDA-MB231 | P4 |
SA183303 | sh CTRL_003 | MDA-MB231 | SCRAMBLE |
SA183304 | sh CTRL_002 | MDA-MB231 | SCRAMBLE |
SA183305 | sh CTRL_001 | MDA-MB231 | SCRAMBLE |
SA183306 | shCtBP2_002 | MDA-MB231 | shCtBP2 |
SA183307 | shCtBP2_003 | MDA-MB231 | shCtBP2 |
SA183308 | shCtBP2_001 | MDA-MB231 | shCtBP2 |
Showing results 1 to 54 of 54 |
Collection:
Collection ID: | CO002012 |
Collection Summary: | MDA-MB231 and MCF102A cell lines were obtained from the American Type Culture Collection (ATCC) (LGC Standard, UK). MDA-MB231 cell line was grown in Dulbecco's modified Eagle's medium (DMEM) containing 4mM L-glutamine, supplemented with 10% fetal bovine serum. MCF102A cell line was maintained in DMEM/F-12 containing 5% horse serum, 2.5mM L-glutamine, 20ng/ml EGF, 100 ng/ml cholera toxin, 0.01 mg/ml insulin, and 500 ng/ml hydrocortisone. All media were supplemented with 100 U/ml penicillin and 100 µg/ml streptomycin, and cells were incubated at 37°C in a 5% CO2 incubator. |
Sample Type: | Breast cancer cells |
Treatment:
Treatment ID: | TR002031 |
Treatment Summary: | cells were plated in 6-well plates with normal growth medium and then incubated for 48h in a complete fresh medium in the presence or absence of treatments (HIPP 400 μM or P4 300 μM) |
Sample Preparation:
Sampleprep ID: | SP002025 |
Sampleprep Summary: | Cells were quickly rinsed with NaCl 0.9% and quenched with 500μl ice-cold 70:30 acetonitrile: water. Plates were placed at -80°C for 10 minutes, collected by scraping, sonicated 5 sec for five pulses at 70% power twice, and then centrifuged at 12000g for 10 min at 4°C. The supernatant was collected in a glass insert and evaporated under airflow at 37°C. Samples were then resuspended with 150 μl of H2O before analyses. |
Combined analysis:
Analysis ID | AN003159 |
---|---|
Analysis type | MS |
Chromatography type | Reversed phase |
Chromatography system | Agilent 1290 Infinity |
Column | Agilent InfinityLab Poroshell 120 HILIC-Z (100 x 2.1mm,2.7um) |
MS Type | ESI |
MS instrument type | QTOF |
MS instrument name | Agilent 6550 QTOF |
Ion Mode | NEGATIVE |
Units | Area |
Chromatography:
Chromatography ID: | CH002337 |
Instrument Name: | Agilent 1290 Infinity |
Column Name: | Agilent InfinityLab Poroshell 120 HILIC-Z (100 x 2.1mm,2.7um) |
Chromatography Type: | Reversed phase |
MS:
MS ID: | MS002939 |
Analysis ID: | AN003159 |
Instrument Name: | Agilent 6550 QTOF |
Instrument Type: | QTOF |
MS Type: | ESI |
MS Comments: | - |
Ion Mode: | NEGATIVE |