Publication : Long chain omega-3 fatty acids and their oxidized metabolites are associated with reduced prostate tumor growth
ali.license-ref | https://creativecommons.org/licenses/by-nc-nd/4.0 | |
ali.license-ref.start-date | 2021-11-18 | |
bul.description.provenance | noadg -- spbar | |
dc.contributor.author | Bilodeau, Jean-François | |
dc.contributor.author | Gevariya, Nikunj | |
dc.contributor.author | Larose, Jessica | |
dc.contributor.author | Robitaille, Karine | |
dc.contributor.author | Fradet, Vincent | |
dc.contributor.author | Roy, Jérôme | |
dc.contributor.author | Oger, Camille | |
dc.contributor.author | Galano, Jean-Marie | |
dc.contributor.author | Bergeron, Alain | |
dc.contributor.author | Durand, Thierry | |
dc.contributor.author | Julien, Pierre | |
dc.contributor.author | Fradet, Yves | |
dc.date.accessioned | 2023-05-24T14:15:57Z | |
dc.date.available | 2023-05-24T14:15:57Z | |
dc.date.issued | 2020-11-18 | |
dc.description.abstract | Introduction: Cancer has been associated with increased oxidative stress and deregulation of bioactive oxylipins derived from long-chain polyunsaturated fatty acids (LC-PUFA) like arachidonic acid (AA). There is a debate whether ω-3 LC-PUFA could promote or prevent prostate tumor growth through immune modulation and reduction of oxidative stress. Our aim was to study the association between enzymatically or non-enzymatically produced oxidized-LC-PUFA metabolites and tumor growth in an immune-competent eugonadal and castrated C57BL/6 male mice injected with TRAMP-C2 prostate tumor cells, fed with ω-3 or ω-6 LC-PUFA-rich diets. Materials and methods: Tumor fatty acids were profiled by gas chromatography and 26 metabolites derived from either AA, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) were assessed by liquid chromatography-mass spectrometry. Results: The enriched ω-3 diet did not reduce oxidative stress overall in tumors but favored the formation of ω-3 rather than ω-6 derived isoprostanoids. We discovered that EPA and its oxidized-derivatives like F3-isoprostanes and prostaglandin (PG)F3Aω, were inversely correlated with tumor volume (spearman correlations and T-test, p<0.05). In contrast, F2-isoprostanes, adrenic acid, docosapentaenoic acid (DPAω-6) and PGE2 were positively correlated with tumor volume. Interestingly, F4-neuroprostanes, PGD2, PGF2ω, and thromboxane were specifically increased in TRAMP-C2 tumors of castrated mice compared to those of eugonadal mice. Discussion: Decreasing tumor growth under ω-3 diet could be attributed in part to increased levels of EPA and its oxidized-derivatives, a reduced level of pro-angiogenic PGE2 and increased levels of F4-neuroprostanes and resolvins content in tumors, suspected of having anti-proliferative and anti-inflammatory effects. | en |
dc.identifier.doi | 10.1016/j.plefa.2020.102215 | |
dc.identifier.issn | 0952-3278 | |
dc.identifier.pubmed | 33276284 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11794/118463 | |
dc.language | eng | |
dc.publisher | Science Direct | |
dc.rights | http://purl.org/coar/access_right/c_abf2 | |
dc.subject | Eugonadal mice | en |
dc.subject | Castrated mice | en |
dc.subject | Inflammation | en |
dc.subject | Oxidative stress | en |
dc.subject | Isoprostanoids | en |
dc.subject | Oxylipins | en |
dc.subject | Anti-prostate cancer effects of omega-3 | en |
dc.subject.rvm | Acides gras oméga 3 | |
dc.subject.rvm | Prostate -- Cancer | |
dc.subject.rvm | Stress oxydatif | |
dc.subject.rvm | Métabolites | |
dc.title | Long chain omega-3 fatty acids and their oxidized metabolites are associated with reduced prostate tumor growth | |
dc.type | article de recherche | |
dcterms.bibliographicCitation | Prostaglandins Leukot Essent Fatty Acids, Vol. 164, 102215 (2021) | |
dcterms.dateAccepted | 2020-11-11 | |
dspace.accessstatus.time | 2023-05-24 18:07:34 | |
dspace.entity.type | Publication | |
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rioxxterms.project.funder-name | Canadian Urology Oncology Group | |
rioxxterms.project.funder-name | Fonds de recherche du Québec - Santé (FRQS) | |
rioxxterms.project.funder-name | Prostate Cancer Canada | |
rioxxterms.version | Accepted Manuscript (AM) | |
rioxxterms.version-of-record | https://doi.org/10.1016/j.plefa.2020.102215 |
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