Summary of Study ST001290

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 PR000872. The data can be accessed directly via it's Project DOI: 10.21228/M8ZT30 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 IDST001290
Study TitleLipidome Signatures of Metastasis in a Transgenic Mouse Model of Sonic Hedgehog Medulloblastoma.
Study TypeUntargeted metabolomics
Study SummaryMetabolic alternations were investigated by applying Ultra Performance Liquid Chromatography Mass Spectrometry (UPLC-MS) to mice brain tissue samples collected from SmoA1-Math-GFP mice with (n=18) and without (n=7) metastasis. All samples were analyzed using reverse phase (RP) UPLC-MS analysis in positive and negative ion modes.
Institute
Georgia Institute of Technology
DepartmentChemistry
LaboratoryFernández
Last NameHuang
First NameDanning
Address901 Atlantic Dr NE
Emaildhuang74@gatech.edu
Phone4045127523
Submit Date2019-12-13
Num Groups2
Total Subjects25
Num Males5
Num Females20
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2020-12-16
Release Version1
Danning Huang Danning Huang
https://dx.doi.org/10.21228/M8ZT30
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR000872
Project DOI:doi: 10.21228/M8ZT30
Project Title:Lipidome Signatures of Metastasis in a Transgenic Mouse Model of Sonic Hedgehog Medulloblastoma.
Project Type:Untargeted metabolomics
Project Summary:Medulloblastoma (MB), the most common malignant pediatric brain tumor, has high propensity to metastasize. Currently, the standard treatment for MB patients includes radiation therapy administered to the entire brain and spine for the purpose of treating or preventing against metastasis. Due to this aggressive treatment, the majority of long-term survivors will be left with permanent and debilitating neurocognitive impairments and, for the 30-40% patients that fail to respond to radiation, all will relapse with terminal metastatic disease. An understanding of the underlying biology that drives MB metastasis is lacking, and is critically needed in order to develop targeted therapeutics for its prevention. To examine the metastatic biology of sonic hedgehog (SHH) MB, the human MB subgroup with the worst clinical outcome, we first generated a robust SmoA1-Math-GFP mouse model that reliably reproduces human SHH MB whereby metastases can be visualized under fluorescence microscopy. Lipidome alterations associated with metastasis were then investigated by applying Ultra-Performance Liquid Chromatography Mass Spectrometry (UPLC-MS) under both positive and negative ionization modes to primary tumor samples collected from mice with (n=18) and without (n=7) metastasis. This study provides the first insights into dysregulations of lipid metabolism associated with SHH MB metastatic progression, and thus serves as a guide toward novel targeted therapies.
Institute:Georgia Institute of Technology
Department:Chemistry
Laboratory:Fernández
Last Name:Huang
First Name:Danning
Address:901 Atlantic Dr NE, Atlanta, GA, 30332, USA
Email:dhuang74@gatech.edu
Phone:404-512-7523

Subject:

Subject ID:SU001362
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:SmoA1-Math-GFP
Age Or Age Range:12-36 weeks
Gender:Male and female
Species Group:Mammals

Factors:

Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Mice strain Group
SA093716SGTA3SmoA1-Math-GFP PT
SA093717SG215SmoA1-Math-GFP PT
SA093718SGTA10SmoA1-Math-GFP PT
SA093719SG105SmoA1-Math-GFP PT
SA093720SG138SmoA1-Math-GFP PT
SA093721CASE40SmoA1-Math-GFP PT
SA093722SG113SmoA1-Math-GFP PT
SA093723SGTA9SmoA1-Math-GFP PT
SA093724SGTA4SmoA1-Math-GFP PT
SA093725SG221SmoA1-Math-GFP PT
SA093726SGTA11SmoA1-Math-GFP PT
SA093727SG218SmoA1-Math-GFP PT
SA093728SG223SmoA1-Math-GFP PT
SA093729SG174SmoA1-Math-GFP PT
SA093730SG203SmoA1-Math-GFP PT
SA093731SG204SmoA1-Math-GFP PT
SA093732SG217SmoA1-Math-GFP PT
SA093733SG175SmoA1-Math-GFP PT
SA093734CASE41SmoA1-Math-GFP PTMT
SA093735SG222SmoA1-Math-GFP PTMT
SA093736SG191SmoA1-Math-GFP PTMT
SA093737SGTA12SmoA1-Math-GFP PTMT
SA093738SGTA13SmoA1-Math-GFP PTMT
SA093739SG228SmoA1-Math-GFP PTMT
SA093740SGTASmoA1-Math-GFP PTMT
Showing results 1 to 25 of 25

Collection:

Collection ID:CO001356
Collection Summary:Mice brain and spinal cord were dissected from each mouse and fluorescence microscopy was used to visualize the tumors. Mice having a GFP signal in the cerebellum only were designated as having a primary tumor without metastasis (PT group, n=18). Mice having a strong GFP signal in the cerebellum and positive GFP signal in the spinal cord were designated as having a primary tumor with metastasis (PTMT group, n=7). With aid of GFP visualization, the primary tumor in each mouse brain was cut from the cerebellum, and immediately frozen using liquid nitrogen, and stored at -80 °C.
Sample Type:Brain
Storage Conditions:-80℃

Treatment:

Treatment ID:TR001377
Treatment Summary:SmoA1-Math1-GFP mice were generated by crossing SmoA1 mice with Math1-driven GFP reporter mice. All mice were kept under the same condition and typically developed detectable MB tumors by MR imaging and clinical symptoms around 23 weeks.

Sample Preparation:

Sampleprep ID:SP001370
Sampleprep Summary:Frozen mice brain tissue samples were cryo-pulverized with liquid nitrogen and weighed. 2-propanol (20 uL/mg) was added to the cryo-pulverized tissue samples to precipitate proteins. Samples were vortex-mixed for 1 min, and centrifuged at 13,000 rpm for 7 min. Following centrifugation, 100 uL of supernatant was transferred to an autosampler vial and analyzed with UPLC-MS. A blank sample, prepared with 100 uL 2-propanol, underwent the same process as the murine tumor samples. A pooled quality control (QC) sample was prepared by mixing a 10 uL aliquot of supernatant of each sample.

Combined analysis:

Analysis ID AN002143 AN002144
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Thermo Dionex Ultimate 3000 Thermo Dionex Ultimate 3000
Column Waters Acquity BEH C18 (50 x 2.1mm,1.7um) Waters Acquity BEH C18 (50 x 2.1mm,1.7um)
MS Type ESI ESI
MS instrument type Orbitrap Orbitrap
MS instrument name Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap
Ion Mode POSITIVE NEGATIVE
Units Normalized Peak Abundance Normalized Peak Abundance

Chromatography:

Chromatography ID:CH001569
Instrument Name:Thermo Dionex Ultimate 3000
Column Name:Waters Acquity BEH C18 (50 x 2.1mm,1.7um)
Column Temperature:55
Sample Injection:5μL
Solvent A:60% acetonitrile/40% water; 0.1% formic acid; 10 mM ammonium formate
Solvent B:90% isopropanol/10% acetonitrile; 0.1% formic acid; 10 mM ammonium formate
Chromatography Type:Reversed phase

MS:

MS ID:MS001995
Analysis ID:AN002143
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:Samples were analyzed in positive and negative ion modes for RP chromatography. Spectral features were extracted from the raw data using Progenesis QI v2.1 software.
Ion Mode:POSITIVE
Capillary Temperature:275 °C
Spray Voltage:3.0 kV
  
MS ID:MS001996
Analysis ID:AN002144
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:Samples were analyzed in positive and negative ion modes for RP chromatography. Spectral features were extracted from the raw data using Progenesis QI v2.1 software.
Ion Mode:NEGATIVE
Capillary Temperature:275 °C
Spray Voltage:-2.8 kV
  logo