4.6 Article

Polyunsaturated Fatty Acids Differentially Modulate Cell Proliferation and Endocannabinoid System in Two Human Cancer Lines

Journal

ARCHIVES OF MEDICAL RESEARCH
Volume 48, Issue 1, Pages 46-54

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.arcmed.2017.01.009

Keywords

Cell proliferation; Endocannabinoid system; Anandamide; Human glioblastoma cells; Human breast cancer cells; Essential fatty acids

Funding

  1. CONICET (Argentina) [PIP 112-200801-03014, SECYT-UNC 05/H297, SECYT-UNLAR 063-2011]
  2. Department of Biotechnology, India

Ask authors/readers for more resources

Background and Aims. Evidence suggests that quantity and quality of dietary polyunsaturated fatty acids (PUFAs) play a role in the development of cancer. However, the mechanisms involved in this interaction(s) are not clear. Endocannabinoids are lipid metabolites known to have growth modulatory actions. We studied the effect of supplementation with PUFAs omega-6 and omega-3 (essential fatty acids, EFAs), saturated and monoun-saturated fatty acids (non-EFAs) on the growth of tumor cells and modifications in their endocannabinoid content. Methods. Cell cultures of human glioblastoma (T98G) and breast cancer (MCF7) were supplemented with 50 or 100 mmol EFAs and non-EFAs for 72 h. Cell proliferation was then determined by MTT, anandamide (AEA) levels by HPLC, total fatty acids profiles by GLC, CB1 receptor expression by WB and FAAH activity by spectrophotometric method. Results. Fatty acids profile reflected the incorporation of the lipids supplemented in each assay. Arachidonic acid (EFA omega-6) supplementation increased AEA levels and inhibited the growth of T98G, whereas palmitic acid (non-EFA) enhanced their proliferation. In breast cancer (MCF7) cells, eicosapentaenoic acid (EFA omega-3) reduced and oleic acid (non-EFA) enhanced their proliferation. CB1 expression was higher in T98G and no differences were observed in FAAH activity. Conclusions. The growth of tumor cells can be differentially modulated by fatty acids and, at least in part, can be attributed to their ability to act on the components of the endocannabinoid system. (c) 2017 IMSS. Published by Elsevier Inc.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available