Article tools
Author information

Research Article

1-O-octadecyl-2-O-methyl-glycerophosphocholine inhibits the transduction of growth signals via the MAPK cascade in cultured MCF-7 cells.

X Zhou, X Lu, C Richard, W Xiong, D W Litchfield, R Bittman and G Arthur

Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.

Published August 15, 1996

1-O-Octadecyl-2-O-methyl-glycerophosphocholine (ET18-OCH3) is an ether lipid with selective antiproliferative properties whose mechanism of action is still unresolved. We hypothesized that since ET18-OCH3 affects a wide variety of cells, its mechanism of action was likely to involve the inhibition of a common widely used pathway for transducing growth signals such as the mitogen-activated protein kinase (MAPK) cascade. To test this, we established conditions whereby quiescent MCF-7 cells took up ET18-OCH3 in sufficient quantities that inhibited cell proliferation subsequent to the addition of growth medium and examined the activation of components of the MAPK cascade under these conditions. ET18-OCH3 inhibited the sustained phosphorylation of MAPK resulting in a decrease in the magnitude and duration of activation of MAPK in cells stimulated with serum or EGF. ET18-OCH3 had no effect on the binding of EGF to its receptors, their activation, or p21ras activation. However, an interference in the association of Raf-1 with membranes and a resultant decrease in Raf-1 kinase activity in membranes of ET18-OCH3-treated cells was observed. ET18-OCH3 had no direct effect on MAPK or Raf-1 kinase activity. A direct correlation between ET18-OCH3 accumulation, inhibition of cell proliferation, Raf association with the membrane, and MAPK activation was also established. These results suggest that inhibition of the MAPK cascade by ET18-OCH3 as a result of its effect on Raf-1 activation may be an important mechanism by which ET18-OCH3 inhibits cell proliferation.

Articles that cite this article:

Antitumour ether lipids: proapoptotic agents with multiple therapeutic indications
Faustino Mollinedo
eotp 17(4):385. doi:10.1517/13543776.17.4.385 [CrossRef]

Characterization of serotonin 5-HT2C receptor signaling to extracellular signal-regulated kinases 1 and 2
Tim D. Werry, Karen J. Gregory, Patrick M. Sexton, Arthur Christopoulos
J Neurochem 93(6):1603. doi:10.1111/j.1471-4159.2005.03161.x [CrossRef]

Enhancement of antitumor activity of the anti-EGF receptor monoclonal antibody cetuximab/C225 by perifosine in PTEN-deficient cancer cells
X Li, R Luwor, Y Lu, K Liang, Z Fan
Oncogenes doi:10.1038/sj.onc.1209075 [CrossRef]

Alkylphospholipids inhibit capillary-like endothelial tube formation in vitro: antiangiogenic properties of a new class of antitumor agents
Shuraila F. Zerp, Stefan R. Vink, Gerald A. Ruiter, Pieter Koolwijk, Erna Peters, Arnold H. Van der luit, Daphne De jong, Marianne Budde, Harry Bartelink, Wim J. Van blitterswijk
Anticancer Drugs 19(1):65. doi:10.1097/CAD.0b013e3282f16d36 [CrossRef]