Summary of Study ST000898

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 PR000624. The data can be accessed directly via it's Project DOI: 10.21228/M8109M 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.

Show all samples  |  Perform analysis on untargeted data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST000898
Study TitleTAp73 is a marker of glutamine addiction in medulloblastoma
Study TypesiRNA constructs targeting p73 (ID: 2671-AMBION) and a non-targeting control siRNA (scramble) were transfected with 10 pM siRNA with lipofectamine 3000 according to the supplier’s protocol for 48 hours
Study SummaryMetabolically-targeted therapies hold the promise of offering an effective and less toxic treatment for tumours including medulloblastoma, the most common malignant brain tumour of childhood. Current treatment relies on the sensitivity of these tumours to DNA damage that was discovered more than 50 years ago. Finding new tumour-specific susceptibilities to complement sensitivity to DNA damage is key to developing new more effective adjuvant therapies. The specific metabolic program of tumours is an attractive vulnerability, as restriction diet are low cost and easy to implement. Here, we present compelling pre-clinical evidence that glutamine restriction diet can be used as an adjuvant treatment for p73-expressing medulloblastoma.
Institute
Queen Mary University of London
DepartmentBlizard Institute
LaboratoryCentre for Genomics and Child Health
Last NameMarino
First NameSilvia
Address4 Newark Street, E1 2AT, London
Emails.marino@qmul.ac.uk
Phone+44 20 7882 2360
Submit Date2017-08-24
Num Groups2
Total Subjects18
Study CommentsWe include 3 biological replicate with 3 technical replicates for each condition.
Raw Data AvailableYes
Analysis Type DetailLC-MS
Release Date2017-11-20
Release Version1
Silvia Marino Silvia Marino
https://dx.doi.org/10.21228/M8109M
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Combined analysis:

Analysis ID AN001460 AN001461
Analysis type MS MS
Chromatography type HILIC HILIC
Chromatography system Waters Acquity I-Class Waters Acquity I-Class
Column Waters Acquity BEH Amide (50 x 2.1mm,1.7um) Waters Acquity BEH Amide (50 x 2.1mm,1.7um)
MS Type ESI ESI
MS instrument type QTOF QTOF
MS instrument name Waters Synapt G2 QTOF Waters Synapt G2 QTOF
Ion Mode POSITIVE NEGATIVE
Units Peak Area Peak Area

Chromatography:

Chromatography ID:CH001027
Chromatography Summary:The samples were analyzed on a Acquity UPLC I-class system from Waters. A HILIC-Amide column (1.7 μm, i.d. 2.1x50 mm) from Waters was used for sample separation and a non-linear gradient elution profile from 100 % A to 100 % B was used. Mobile phase A consisted of 90:10 acetonitrile/water with 10 mM ammonium formate and 0.1% FA while mobile phase B consisted of 50:50 acetonitrile/ water with 10 mM ammonium formate and 0.1% FA. The flow rate was 0.3 ml/min, the column temperature 40°C and the injection volume 5 µL.
Instrument Name:Waters Acquity I-Class
Column Name:Waters Acquity BEH Amide (50 x 2.1mm,1.7um)
Column Temperature:40°C
Flow Gradient:Non-linear gradient elution profile from 100 % A to 100 % B was used. In detail; 100% A was kept for 0.5 min then decreased non-linearly (slope-factor 8 in MassLynx) over 12.5 min to 100% B, 100% B was held for 3 min followed by 7 min at 100 % A to re-equilibrate the column for a total run-time of 23 min.
Flow Rate:0.3 ml/min
Injection Temperature:4°C
Sample Injection:5 μl
Solvent A:90% acetonitrile/10% water; 0.1% formic acid; 10 mM ammonium formate
Solvent B:50% acetonitrile/50% water; 0.1% formic acid; 10 mM ammonium formate
Analytical Time:23 min total sample run-time
Randomization Order:All samples were analyzed in a randomized order with three QC injections interspaced every eleventh injection
Chromatography Type:HILIC
  logo