Summary of project PR002629

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 PR002629. The data can be accessed directly via it's Project DOI: 10.21228/M8TK1K This work is supported by NIH grant, U2C- DK119886. See: https://www.metabolomicsworkbench.org/about/howtocite.php

Project ID: PR002629
Project DOI:doi: 10.21228/M8TK1K
Project Title:Alanine catabolism as a targetable vulnerability for MYC-driven liver cancer
Project Summary:The aim was to compare how alanine is metabolized in MYC-driven liver tumors versus non-tumor liver tissue. Liver tumor bearing mice were infused with C13/N15 alanine, and kidney, liver tumor, and non tumor liver tissue were harvested. Kidney was used as an internal positive control, since the kidney is a known site of alanine metabolism. We found that on average ~35% of the tumor alanine pool had at least one heavy isotope label, thus confirming the efficacy of our tracing strategy. We uncovered a repertoire of pathways downstream of alanine, with multiple metabolites being preferentially labelled in tumor versus non-tumor tissue. Among the pathways fed by alanine in tumors were metabolites relating to cellular bioenergetics, biosynthesis, and the oxidative stress response. Thus our study identified how alanine is a substrate for metabolism in MYC-driven liver tumors.
Institute:University of California, San Francisco
Department:Cell & Tissue Biology
Last Name:Montoya
First Name:Tonatiuh
Address:513 Parnassus Ave
Email:Tonatiuh.Montoya@ucsf.edu
Phone:415-476-4187

Summary of all studies in project PR002629

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ST004169 Alanine catabolism as a targetable vulnerability for MYC-driven liver cancer Mus musculus University of California, San Francisco MS 2026-01-12 1 21 Uploaded data (2.1G)*
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