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

I. Brown*, K. W.J. Wahle, M. G. Cascio, R. Smoum-Jaouni, R. Mechoulam, R. G. Pertwee, S. D. Heys

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

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.

Original languageEnglish
Pages (from-to)305-310
Number of pages6
JournalProstaglandins Leukotrienes and Essential Fatty Acids
Volume85
Issue number6
DOIs
StatePublished - Dec 2011

Bibliographical note

Funding Information:
Sources of support: This work was supported by Grants from the National Institutes of Health (DA-009789), TENOVUS Scotland, and NHS Grampian Endowments fund.

Keywords

  • Breast cancer
  • Endocannabinoid
  • N-3 PUFA
  • N-acylethanolamine
  • Prostate cancer

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