Vaccenic acid (t11-18:1) is converted to c9,t11-CLA in MCF-7 and SW480 cancer cells

Lipids. 2003 Jun;38(6):623-32. doi: 10.1007/s11745-003-1107-8.

Abstract

The aims of this study were to determine whether vaccenic acid (VA; t11-18:1) is converted to c9,t11-CLA in human mammary (MCF-7) and colon (SW480) cancer cell lines and whether VA influences cell viability and other CLA-bioresponsive markers. When cells were incubated in the presence of VA at concentrations of 5 to 20 microg/mL, both VA and c9,t11-CLA increased in cellular lipids in a dose-dependent manner. After 4 d of incubation of SW480 and MCF-7 cells with VA (20 microg/mL), c9,t11-CLA increased from undetectable levels to 8.57 and 12.14 g/100 g FAME in cellular lipids, respectively. VA supplementation for 4 d at 5, 10, and 15 microg/mL had no effect on cell growth, whereas 20 microg/mL significantly (P < 0.05) reduced cell growth in both cell lines. VA (20 microg/mL) treatment induced DNA fragmentation and significantly (P < 0.05) depleted cytosolic GSH levels in the SW480 cell line after 4 d of incubation, suggesting that apoptosis was the mode of cell death induced by VA. Both VA and c9,t11-CLA reduced (P < 0.05) total ras expression in SW480 cells. 14C-Arachidonic acid uptake into the MG fraction was significantly increased (P < 0.05) in both cell lines while uptake into the phospholipid fraction decreased in response to VA. VA treatment significantly (P < 0.05) increased 8-epi-prostaglandin F2alpha in both cell lines. The data indicate that growth suppression and cellular responses of both cells lines are likely mediated by VA desaturation to c9,t11-CLA via delta9-desaturase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Arachidonic Acid / metabolism
  • Biotransformation
  • Carbon Radioisotopes
  • Cell Line, Tumor
  • Chromatography, Thin Layer
  • Fatty Acids / analysis*
  • Glycerides / metabolism
  • Humans
  • Linoleic Acids, Conjugated / chemistry
  • Linoleic Acids, Conjugated / metabolism*
  • Oleic Acids / chemistry
  • Oleic Acids / metabolism*
  • Oleic Acids / pharmacology
  • Phospholipids / metabolism
  • Prostaglandins / metabolism

Substances

  • Carbon Radioisotopes
  • Fatty Acids
  • Glycerides
  • Linoleic Acids, Conjugated
  • Oleic Acids
  • Phospholipids
  • Prostaglandins
  • Arachidonic Acid
  • 11-octadecenoic acid