Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/126846
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Type: Journal article
Title: Human DECR1 is an androgen-repressed survival factor that regulates PUFA oxidation to protect prostate tumor cells from ferroptosis
Author: Nassar, Z.D.
Mah, C.Y.
Dehairs, J.
Burvenich, I.J.
Irani, S.
Centenera, M.M.
Helm, M.
Shrestha, R.K.
Moldovan, M.
Don, A.S.
Holst, J.
Scott, A.M.
Horvath, L.G.
Lynn, D.J.
Selth, L.A.
Hoy, A.J.
Swinnen, J.V.
Butler, L.M.
Citation: eLife, 2020; 9:1-34
Publisher: eLife
Issue Date: 2020
ISSN: 2050-084X
2050-084X
Statement of
Responsibility: 
Zeyad D Nassar, Chui Yan Mah, Jonas Dehairs, Ingrid JG Burvenich ... Lisa M Butler ... Luke Selth ... et al.
Abstract: Fatty acid β-oxidation (FAO) is the main bioenergetic pathway in human prostate cancer (PCa) and a promising novel therapeutic vulnerability. Here we demonstrate therapeutic efficacy of targeting FAO in clinical prostate tumors cultured ex vivo, and identify DECR1, encoding the rate-limiting enzyme for oxidation of polyunsaturated fatty acids (PUFAs), as robustly overexpressed in PCa tissues and associated with shorter relapse-free survival. DECR1 is a negatively-regulated androgen receptor (AR) target gene and, therefore, may promote PCa cell survival and resistance to AR targeting therapeutics. DECR1 knockdown selectively inhibited β-oxidation of PUFAs, inhibited proliferation and migration of PCa cells, including treatment resistant lines, and suppressed tumor cell proliferation and metastasis in mouse xenograft models. Mechanistically, targeting of DECR1 caused cellular accumulation of PUFAs, enhanced mitochondrial oxidative stress and lipid peroxidation, and induced ferroptosis. These findings implicate PUFA oxidation via DECR1 as an unexplored facet of FAO that promotes survival of PCa cells.
Keywords: androgen
cancer biology
ferroptosis
human
lipid metabolism
mouse
prostate cancer
Rights: Copyright Nassar et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
DOI: 10.7554/eLife.54166
Grant ID: http://purl.org/au-research/grants/nhmrc/1121057
http://purl.org/au-research/grants/nhmrc/1084178
http://purl.org/au-research/grants/nhmrc/1138648
http://purl.org/au-research/grants/nhmrc/1100626
http://purl.org/au-research/grants/arc/FT130101004
http://purl.org/au-research/grants/nhmrc/1138648
http://purl.org/au-research/grants/nhmrc/1121057
http://purl.org/au-research/grants/nhmrc/1100626
http://purl.org/au-research/grants/nhmrc/1084178
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