Summary of project PR001786

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 PR001786. The data can be accessed directly via it's Project DOI: 10.21228/M8VB1G This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

Project ID: PR001786
Project DOI:doi: 10.21228/M8VB1G
Project Title:MYC is a regulator of androgen receptor inhibition-induced metabolic requirements in prostate cancer
Project Summary:Advanced prostate cancers are treated with therapies targeting the androgen receptor (AR) signaling pathway. While many tumors initially respond to AR inhibition, nearly all develop resistance. It is critical to understand how prostate tumor cells respond to AR inhibition in order to exploit therapy-induced phenotypes prior to the outgrowth of treatment-resistant disease. Here, we comprehensively characterize the effect of AR blockade on prostate cancer metabolism using transcriptomics, metabolomics and bioenergetics approaches. The metabolic response to AR inhibition is defined by reduced glycolysis, robust elongation of mitochondria, and increased reliance on mitochondrial oxidative metabolism. We establish DRP1 activity and MYC signaling as mediators of AR blockade-induced metabolic phenotypes. Rescuing DRP1 phosphorylation after AR inhibition restores mitochondrial fission, while rescuing MYC restores glycolytic activity and prevents sensitivity to complex I inhibition. Our study provides new insight into the regulation of treatment-induced metabolic phenotypes and vulnerabilities in prostate cancer.
Institute:University of California, Los Angeles
Department:Biological Chemistry
Laboratory:Heather Christofk
Last Name:Matulionis
First Name:Nedas
Address:615 Charles E Young Dr S, BSRB 354-05
Email:nmatulionis@mednet.ucla.edu
Phone:3102060163

Summary of all studies in project PR001786

Study IDStudy TitleSpeciesInstituteAnalysis
(* : Contains Untargted data)
Release
Date
VersionSamplesDownload
(* : Contains raw data)
ST002852 MYC is a regulator of androgen receptor inhibition-induced metabolic requirements in prostate cancer Mus musculus University of California, Los Angeles MS 2023-09-11 1 16 Uploaded data (1G)*
ST002863 Metabolic profiling and glucose tracing in naive and Enzalutamide-treated 16D prostate cancer cells Homo sapiens University of California, Los Angeles MS 2023-09-19 1 14 Uploaded data (1.7G)*
ST002864 Metabolic profiling, glucose tracing and glutamine tracing in naive and Enzalutamide-treated 16D prostate cancer cells expressing RFP or MYC Homo sapiens University of California, Los Angeles MS 2023-09-19 1 27 Uploaded data (6.5G)*
ST002865 Metabolic profiling, glucose tracing and glutamine tracing in 16D prostate cancer cells treated with vehicle, AR inhibitor Enzalutamide, AR inhibitor Apalutamide, or AR degrader/PROTAC ARCC-4 Homo sapiens University of California, Los Angeles MS 2023-09-19 1 27 Uploaded data (6.4G)*
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