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Research Article| Volume 85, ISSUE 6, P305-310, December 2011

Omega-3 N-acylethanolamines are endogenously synthesised from omega-3 fatty acids in different human prostate and breast cancer cell lines

  • I. Brown
    Correspondence
    Corresponding author at: Division of Applied Medicine, University of Aberdeen, Polwarth Building, Aberdeen, AB25 2ZD, UK. Tel.: +44 1224 558989; fax: +44 1224 437348.
    Affiliations
    Translational Medical Sciences, Division of Applied Medicine, School of Medicine and Dentistry, University of Aberdeen, Aberdeen, AB25 2ZD, UK
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  • K.W.J. Wahle
    Affiliations
    Translational Medical Sciences, Division of Applied Medicine, School of Medicine and Dentistry, University of Aberdeen, Aberdeen, AB25 2ZD, UK

    Neurobiology Research Programme, School of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, UK

    Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK
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  • M.G. Cascio
    Affiliations
    Neurobiology Research Programme, School of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, UK
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  • R. Smoum-Jaouni
    Affiliations
    Faculty of Medicine, Hebrew University, Ein Kerem Campus, 91120 Jerusalem, Israel
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  • R. Mechoulam
    Affiliations
    Faculty of Medicine, Hebrew University, Ein Kerem Campus, 91120 Jerusalem, Israel
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  • R.G. Pertwee
    Affiliations
    Neurobiology Research Programme, School of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, UK
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  • S.D. Heys
    Affiliations
    Translational Medical Sciences, Division of Applied Medicine, School of Medicine and Dentistry, University of Aberdeen, Aberdeen, AB25 2ZD, UK
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Published:October 13, 2011DOI:https://doi.org/10.1016/j.plefa.2011.09.007

      Abstract

      Omega-3 (n-3) fatty acids inhibit breast and prostate cancer cell growth. We previously showed that N-acylethanolamine derivatives of n-3 (n-3-NAE) are endocannabinoids, which regulate cancer cell proliferation. These n-3-NAE are synthesised in certain cells/tissues, after supplementing with fatty acids, however, no one has assessed whether and to what extent this occurs in cancer cells. We determined levels of endogenous n-3-NAEs in hormone sensitive and insensitive prostate and breast cancer cells and subsequent effects on other endocannabinoids (anandamide and 2-arachidonoylglycerol), before and after supplementing with DHA and EPA fatty acids, using HPLC tandem mass spectrometry. This is the first study reporting that n-3-NAEs are synthesised from their parent n-3 fatty acids in cancer cells, regardless of tumour type, hormone status or the presence of fatty acid amide hydrolase. This could have important implications for the use of n-3 fatty acids as therapeutic agents in breast and prostate cancers expressing cannabinoid receptors.

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