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Data from ELOVL5 Is a Critical and Targetable Fatty Acid Elongase in Prostate Cancer

Posted on 2023-03-31 - 04:26
Abstract

The androgen receptor (AR) is the key oncogenic driver of prostate cancer, and despite implementation of novel AR targeting therapies, outcomes for metastatic disease remain dismal. There is an urgent need to better understand androgen-regulated cellular processes to more effectively target the AR dependence of prostate cancer cells through new therapeutic vulnerabilities. Transcriptomic studies have consistently identified lipid metabolism as a hallmark of enhanced AR signaling in prostate cancer, yet the relationship between AR and the lipidome remains undefined. Using mass spectrometry–based lipidomics, this study reveals increased fatty acyl chain length in phospholipids from prostate cancer cells and patient-derived explants as one of the most striking androgen-regulated changes to lipid metabolism. Potent and direct AR-mediated induction of ELOVL fatty acid elongase 5 (ELOVL5), an enzyme that catalyzes fatty acid elongation, was demonstrated in prostate cancer cells, xenografts, and clinical tumors. Assessment of mRNA and protein in large-scale data sets revealed ELOVL5 as the predominant ELOVL expressed and upregulated in prostate cancer compared with nonmalignant prostate. ELOVL5 depletion markedly altered mitochondrial morphology and function, leading to excess generation of reactive oxygen species and resulting in suppression of prostate cancer cell proliferation, 3D growth, and in vivo tumor growth and metastasis. Supplementation with the monounsaturated fatty acid cis-vaccenic acid, a direct product of ELOVL5 elongation, reversed the oxidative stress and associated cell proliferation and migration effects of ELOVL5 knockdown. Collectively, these results identify lipid elongation as a protumorigenic metabolic pathway in prostate cancer that is androgen-regulated, critical for metastasis, and targetable via ELOVL5.

Significance:

This study identifies phospholipid elongation as a new metabolic target of androgen action that is critical for prostate tumor metastasis.

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FUNDING

Movember Foundation and Prostate Cancer Foundation of Australia

Prostate Cancer Foundation of Australia

the Research Foundation–Flanders

the Stichting tegen Kanker

KU Leuven

Interreg V-A

the National Health and Medical Research Council

the National Institute of Health

NCI

the United States Department of Defense

National Health and Medical Research Council Early Career Fellowship

Department of Health, and the Australian Government through the Medical Research Future Fund

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Cancer Research

AUTHORS (33)

  • Margaret M. Centenera
    Julia S. Scott
    Jelle Machiels
    Zeyad D. Nassar
    Deanna C. Miller
    Irene Zinonos
    Jonas Dehairs
    Ingrid J.G. Burvenich
    Giorgia Zadra
    Paolo M. Chetta
    Clyde Bango
    Emma Evergren
    Natalie K. Ryan
    Joanna L. Gillis
    Chui Yan Mah
    Terence Tieu
    Adrienne R. Hanson
    Ryan Carelli
    Katarzyna Bloch
    Vasilios Panagopoulos

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