Summary of Study ST003184

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 PR001983. The data can be accessed directly via it's Project DOI: 10.21228/M8D72S This work is supported by NIH grant, U2C- DK119886.

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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 IDST003184
Study TitleA multimodal drug-diet-immunotherapy combination restrains melanoma progression and metastasis - tumor lipidomics
Study SummaryLipidomics profiling of immunocompetent B16F10 model of melanoma to examine lipid levels in tumors following reduced oleic acid content in diet combined with the stearyl CoA desaturase inhibitor CAY10566.
Institute
University of Colorado Anschutz Medical Campus
Last NameHaines
First NameJulie
Address12801 E 17th Ave, Room 1303, Aurora, Colorado, 80045, USA
Emailjulie.haines@cuanschutz.edu
Phone3037243339
Submit Date2024-05-01
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2024-05-18
Release Version1
Julie Haines Julie Haines
https://dx.doi.org/10.21228/M8D72S
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001983
Project DOI:doi: 10.21228/M8D72S
Project Title:A multimodal drug-diet-immunotherapy combination restrains melanoma progression and metastasis
Project Summary:The genetic landscape of cancer cells can lead to specific metabolic dependencies for tumor growth. Dietary interventions represent an attractive strategy to restrict the availability of key nutrients to tumors. In this study, we identified that growth of a subset of melanoma was severely restricted by a rationally designed combination therapy of a stearoyl-CoA desaturase (SCD) inhibitor with an isocaloric low-oleic acid diet. Despite its importance in oncogenesis, SCD underwent monoallelic co-deletion along with PTEN on chromosome 10q in about 47.5% of melanoma, and the other SCD allele was methylated, resulting in very low SCD expression. While this SCD deficient subset was refractory to SCD inhibitors, the subset of PTEN wildtype melanoma that retained SCD was sensitive. As dietary oleic acid could potentially blunt the effect of SCD inhibitors, a low-oleic acid custom diet was combined with SCD inhibitor. The combination reduced monounsaturated fatty acids and increased saturated fatty acids, inducing robust apoptosis and growth suppression and inhibiting lung metastasis with minimal toxicity in preclinical mouse models of PTEN wildtype melanoma. When combined with anti-PD1 immunotherapy, the SCD inhibitor improved T cell functionality and further constrained melanoma growth in mice. Collectively, these results suggest that optimizing SCD inhibitors with diets low in oleic acid may offer a viable and efficacious therapeutic approach for improving melanoma treatment.
Institute:University of Colorado Anschutz Medical Campus
Laboratory:Lab of Angelo D'Alessandro in collaboration with lab of Biplab Dasgupta
Last Name:Haines
First Name:Julie
Address:12801 E 17th Ave, Room 1303, Aurora, Colorado, 80045, USA
Email:julie.haines@cuanschutz.edu
Phone:3037243339

Subject:

Subject ID:SU003303
Subject Type:Mammal
Subject Species:Mus musculus
Gender:Not applicable
Species Group:Mammals

Factors:

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

mb_sample_id local_sample_id factor
SA346767DS2-039-016SCD inhibitor + high oleic acid diet
SA346768DS2-039-017SCD inhibitor + high oleic acid diet
SA346769DS2-039-018SCD inhibitor + high oleic acid diet
SA346770DS2-039-019SCD inhibitor + high oleic acid diet
SA346771DS2-039-020SCD inhibitor + high oleic acid diet
SA346772DS2-039-010SCD inhibitor + low oleic acid diet
SA346773DS2-039-009SCD inhibitor + low oleic acid diet
SA346774DS2-039-007SCD inhibitor + low oleic acid diet
SA346775DS2-039-006SCD inhibitor + low oleic acid diet
SA346776DS2-039-008SCD inhibitor + low oleic acid diet
SA346777DS2-039-015Vehicle + high oleic acid diet
SA346778DS2-039-014Vehicle + high oleic acid diet
SA346779DS2-039-011Vehicle + high oleic acid diet
SA346780DS2-039-013Vehicle + high oleic acid diet
SA346781DS2-039-012Vehicle + high oleic acid diet
SA346782DS2-039-003Vehicle+ low oleic acid diet
SA346783DS2-039-002Vehicle+ low oleic acid diet
SA346784DS2-039-005Vehicle+ low oleic acid diet
SA346785DS2-039-001Vehicle+ low oleic acid diet
SA346786DS2-039-004Vehicle+ low oleic acid diet
Showing results 1 to 20 of 20

Collection:

Collection ID:CO003296
Collection Summary:Mice were randomized into groups with combinations of sunflower or coconut oil diet, and vehicle or CAY10566. B16F10 cells were implanted in the flank of C57BL/6 mice. Mice were treated with vehicle or CAY10566 at 30 mg/kg twice daily by oral gavage three days after tumor cell implantation (bilateral tumors in n=4 per group). Mice were euthanized and lungs were harvested 17 days after tumor cell injection/14 days after the start of treatment.
Sample Type:Tumor cells

Treatment:

Treatment ID:TR003312
Treatment Summary:All animal procedures were carried out in accordance with the IACUC-approved protocol of Cincinnati Children’s Hospital Medical Center. Animals were monitored daily by Veterinary Services. For subcutaneous tumor implantation, 1x10^6 B16F10 cells were mixed with matrigel 1:1 and implanted subcutaneously into NOD-SCID IL2Rgnull or C57BL/6 mice, respectively. CAY10566 was suspended in 0.5% Methyl Cellulose in water with 0.2% Tween 80 at 9 parts per 1 part DMSO stock. CAY10566 was administered at 30mg/kg via oral gavage, twice daily, with a drug holiday during the weekends.

Sample Preparation:

Sampleprep ID:SP003310
Sampleprep Summary:For tumor analysis, tissue was weighed and placed into 1.5mL Eppendorf Safe-Lock tubes that were pre-filled with 1.0mm glass grinder beads (Biospec Products Inc). Cold methanol was then added to each tube so that all final tissue concentrations were 20 mg/mL. Samples were then homogenized via a “Next Advance” Bullet Blender for 5 minutes and subsequently vortexed for 30 minutes. Following vortex, insoluble material was pelleted by centrifugation (18000g, 10 min) and supernatants were isolated for analysis by UHPLC-MS.
Processing Storage Conditions:4℃
Extract Storage:-80℃

Chromatography:

Chromatography ID:CH003955
Chromatography Summary:Negative C18 global lipidomics
Instrument Name:Thermo Vanquish
Column Name:Phenomenex Kinetex C18 (30 x 2.1mm,1.7um)
Column Temperature:45
Flow Gradient:0-3 min 10-95% B at 0.3 mL/min, 3-4.2 min hold at 95% B at 0.3 mL/min, 4.2-4.3 min drop to 10% B at 0.45 mL/min, 4.3-4.9 min hold at 10%B while lowering flow rate to 0.4 mL/min, 4.9-5 min hold at 10%B while lowering flow rate to 0.3 mL/min.
Flow Rate:0.3-0.4 ml/min
Sample Injection:10 uL
Solvent A:75% water/25% acetonitrile; 5 mM ammonium acetate
Solvent B:90% isopropanol/10% acetonitrile; 5 mM ammonium acetate
Chromatography Type:Reversed phase
  
Chromatography ID:CH003956
Chromatography Summary:Positive C18 global lipidomics
Instrument Name:Thermo Vanquish
Column Name:Phenomenex Kinetex C18 (30 x 2.1mm,1.7um)
Column Temperature:45
Flow Gradient:0-3 min 30-100% B at 0.3 mL/min, 3-4.2 min hold at 100% B at 0.3 mL/min, 4.2-4.3 min 100-30% B at 0.4 mL/min, 4.3-4.9 min hold at 30%B and 0.4 mL/min, 4.9-5 min hold at 30%B while lowering flow rate to 0.3 mL/min
Flow Rate:0.3-0.4 ml/min
Sample Injection:10 uL
Solvent A:75% water/25% acetonitrile; 5 mM ammonium acetate
Solvent B:90% isopropanol/10% acetonitrile; 5 mM ammonium acetate
Chromatography Type:Reversed phase
  
Chromatography ID:CH003957
Chromatography Summary:Negative C18 fatty acids
Instrument Name:Thermo Vanquish
Column Name:Waters ACQUITY UPLC HSS T3 (150 x 2.1mm,1.8um)
Column Temperature:45
Flow Gradient:0-1 min 25% B and 0.3 ml/min; 1-2 min 25-50% B and 0.3 mL/min; 2–8 min 50–90% B and 0.3 mL/min; 8–10 min 90–99% B and 0.3 mL/min; 10–14 min hold at 99% B and 0.3 mL/min; 14–14.1 min 99–25% B and 0.3 mL/min; 14.1–16.9 min hold at 25% B and 0.4 mL/min; 16.9–17 min hold at 25% B and resume flow of 0.3 mL/min
Flow Rate:0.3-0.4 ml/min
Solvent A:75% water/25% acetonitrile; 5 mM ammonium acetate
Solvent B:50% isopropanol/45% acetonitrile/5% water; 5 mM ammonium acetate
Chromatography Type:Reversed phase

Analysis:

Analysis ID:AN005228
Analysis Type:MS
Chromatography ID:CH003955
Num Factors:4
Num Metabolites:279
Rt Units:Minutes
Units:peak area
  
Analysis ID:AN005229
Analysis Type:MS
Chromatography ID:CH003956
Num Factors:4
Num Metabolites:618
Rt Units:Minutes
Units:peak area
  
Analysis ID:AN005230
Analysis Type:MS
Chromatography ID:CH003957
Num Factors:4
Num Metabolites:9
Rt Units:Minutes
Units:peak area
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