Summary of Study ST003479

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 PR002137. The data can be accessed directly via it's Project DOI: 10.21228/M8CZ33 This work is supported by NIH grant, U2C- DK119886.

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Study IDST003479
Study TitleFatty acid analysis of similarly sized MC38 tumors from control-diet- or high-fat-diet-fed C57BL/6 mice revealed an increase in tumoral oleic acid in high-fat-diet-fed mice.
Study SummarySimilarly sized MC38 tumors from control-diet- and high-fat-diet-fed mice were subject to fatty acid analysis via GC-FID. These data revealed an increase in oleic acid in tumors from high-fat-diet-fed mice. Oleic acid was the only fatty acid to exhibit this trend.
Institute
Stanford University
Last NameBagchi
First NameSreya
Address3373 Hillview Avenue
Emailbagchipuja@gmail.com
Phone4086214773
Submit Date2024-08-12
Analysis Type DetailOther
Release Date2024-10-18
Release Version1
Sreya Bagchi Sreya Bagchi
https://dx.doi.org/10.21228/M8CZ33
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR002137
Project DOI:doi: 10.21228/M8CZ33
Project Title:Acid-sensing receptor, GPR65, on tumor macrophages drives accelerated tumor growth in obesity
Project Summary:Multiple cancers, including colorectal cancer (CRC), are more frequent and often more aggressive in obese individuals. Here, we show that macrophages accumulate within tumors of obese CRC patients and in obese CRC mice and promote accelerated tumor growth. These changes are initiated by oleic acid accumulation and subsequent tumor cell-derived acid production, and driven by signaling through GPR65, an acid-sensing receptor on CRC-associated macrophages. We demonstrate a similar role for GPR65 in hepatocellular carcinoma (HCC) in obese mice. Tumors in obese patients with CRC or HCC also exhibit increased GPR65 expression, suggesting that the mechanism revealed here likely contributes to tumor growth in a range of obesity-associated cancers and represents a potential therapeutic target.
Institute:Stanford University
Last Name:Bagchi
First Name:Sreya
Address:3373 Hillview Avenue
Email:sbagchi@stanford.edu
Phone:4086214773

Subject:

Subject ID:SU003607
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6J

Factors:

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

mb_sample_id local_sample_id Sample source Treatment
SA38373514MC38 murine whole tumor CD- different size tumor
SA3837369MC38 murine whole tumor CD- different size tumor
SA38373715MC38 murine whole tumor CD- different size tumor
SA3837388MC38 murine whole tumor CD- different size tumor
SA38373913MC38 murine whole tumor CD- different size tumor
SA38374012MC38 murine whole tumor CD- different size tumor
SA38374111MC38 murine whole tumor CD- different size tumor
SA38374210MC38 murine whole tumor CD- different size tumor
SA38374316MC38 murine whole tumor HFD- different size tumor
SA38374418MC38 murine whole tumor HFD- different size tumor
SA38374519MC38 murine whole tumor HFD- different size tumor
SA38374620MC38 murine whole tumor HFD- different size tumor
SA38374721MC38 murine whole tumor HFD- different size tumor
SA38374822MC38 murine whole tumor HFD- different size tumor
SA38374923MC38 murine whole tumor HFD- different size tumor
SA38375024MC38 murine whole tumor HFD- different size tumor
SA38375117MC38 murine whole tumor HFD- different size tumor
Showing results 1 to 17 of 17

Collection:

Collection ID:CO003600
Collection Summary:MC38 tumors were isolated from control and high-fat diet fed mice, 21 days post tumor implantation.
Sample Type:Whole tumor

Treatment:

Treatment ID:TR003616
Treatment Summary:Mice were divided into two groups- control and high-fat diet fed. Mice were fed the respective diets for 2 months starting at the age of 2 months. Subsequently tumor cells were injected to induce tumor growth.

Sample Preparation:

Sampleprep ID:SP003614
Sampleprep Summary:Whole tumors were isolated and immediately snap frozen and sent for fatty acid analysis.
Sampleprep Protocol Filename:MC38_fatty_acid_GC_protocol.pdf

Combined analysis:

Analysis ID AN005714
Analysis type MS
Chromatography type GC
Chromatography system Agilent 6890N
Column Agilent DB-23 (60m x 0.25mm, 0.25um)
MS Type Other
MS instrument type Other
MS instrument name N/A (FID detection was used)
Ion Mode UNSPECIFIED
Units nmol/mg dry wt

Chromatography:

Chromatography ID:CH004335
Chromatography Summary:GC-FID was performed on an Agilent 6890N GC coupled to a FID ( flame ionization detector). The FID detector was operated at 260 °C. The hydrogen flow to the detector was 30 mL/min and air flow was 400 mL/min. The sampling rate of the FID was 20 Hz.
Methods Filename:MC38_fatty_acid_GC_protocol.pdf
Instrument Name:Agilent 6890N
Column Name:Agilent DB-23 (60m x 0.25mm, 0.25um)
Column Temperature:250
Flow Gradient:Temperature-programmed GC
Flow Rate:1.5 mL/min
Internal Standard:pentadecanoic acid (15:0)
Solvent A:3 M methanolic hydrochloric acid
Solvent B:100% hexane
Chromatography Type:GC

MS:

MS ID:MS005437
Analysis ID:AN005714
Instrument Name:N/A (FID detection was used)
Instrument Type:Other
MS Type:Other
MS Comments:No MS involved (FID detection was used)
Ion Mode:UNSPECIFIED
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