The role of cyclooxygenase in n-6 and n-3 polyunsaturated fatty acid mediated effects on cell proliferation, PGE(2) synthesis and cytotoxicity in human colorectal carcinoma cell lines

• Published in: Carcinogenesis (New York) Vol. 24; no. 3; p. 385
• Main Authors: Dommels, Yvonne E M, Haring, Merel M G, Keestra, Nynke G M, Alink, Gerrit M, van Bladeren, Peter J, van Ommen, Ben
• Format: Journal Article
• Language: English
• Published: England 01.03.2003
• Subjects: Antioxidants - pharmacology; Caco-2 Cells; Cell Division - drug effects; Colorectal Neoplasms - enzymology; Colorectal Neoplasms - metabolism; Colorectal Neoplasms - pathology; Cyclooxygenase Inhibitors - pharmacology; Dinoprostone - biosynthesis; Fatty Acids, Omega-3 - pharmacology; Fatty Acids, Omega-6; Fatty Acids, Unsaturated - pharmacology; HT29 Cells; Humans; Lipid Peroxidation; Prostaglandin-Endoperoxide Synthases - metabolism
• ISSN: 0143-3334
• DOI: 10.1093/carcin/24.3.385

This study was conducted to investigate the role of the enzyme cyclooxygenase (COX) and its prostaglandin product PGE(2) in n-6 and n-3 polyunsaturated fatty acid (PUFA)-mediated effects on cellular proliferation of two human colorectal carcinoma cell lines. The long chain PUFAs eicosapentaenoic acid (EPA; 20:5n-3) and arachidonic acid (AA; 20:4n-6) both inhibited cell proliferation of Caco-2 cells compared with the long chain fatty acids alpha-linolenic acid (ALA; 18:3n-3) and linoleic acid (LA; 18:2n-6). Neither incubation with PGE(2) nor reduction in PGE(2) synthesis by EPA compared with AA led to differential effects on cell proliferation in Caco-2 cells. This suggests that n-6 and n-3 PUFA-mediated cell proliferation in Caco-2 cells is not regulated via PGE(2) levels. AA and EPA had no effect on growth of HT-29 colon cancer cells with a low COX activity. However, stimulation of COX-2 activity by IL-1 beta resulted in a decrease in cell proliferation and an induction of cytotoxicity by AA as well as by EPA. Both inhibition of the COX pathway by indomethacin as well as inhibition of direct lipid peroxidation by antioxidants such as vitamin E and C diminished the anti-proliferative effects of AA as well as EPA. Also, malondialdehyde, a product of lipid peroxidation and COX-activity was decreased by addition of vitamin E and partially decreased by indomethacin. These data support the hypothesis that growth inhibitory and cytotoxic effects of PUFAs with methylene-interrupted double bonds such as AA and EPA are due to peroxidation products that are generated during lipid peroxidation and COX activity.