Zhou X, Lu X, Richard C, Xiong W, Litchfield D W, Bittman R, Arthur G
Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
J Clin Invest. 1996 Aug 15;98(4):937-44. doi: 10.1172/JCI118877.
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.
1-油酰基-2-甲基甘油磷酸胆碱(ET18-OCH3)是一种具有选择性抗增殖特性的醚脂,其作用机制仍未明确。我们推测,由于ET18-OCH3对多种细胞都有影响,其作用机制可能涉及抑制一种常见的广泛用于转导生长信号的途径,如丝裂原活化蛋白激酶(MAPK)级联反应。为了验证这一点,我们建立了一种条件,使静止的MCF-7细胞摄取足够量的ET18-OCH3,在添加生长培养基后抑制细胞增殖,并在这些条件下检测MAPK级联反应各组分的激活情况。ET18-OCH3抑制了MAPK的持续磷酸化,导致在用血清或表皮生长因子(EGF)刺激的细胞中,MAPK激活的幅度和持续时间降低。ET18-OCH3对EGF与其受体的结合、受体的激活或p21ras的激活没有影响。然而,观察到ET18-OCH3处理的细胞中,Raf-1与膜的结合受到干扰,膜中Raf-1激酶活性随之降低。ET18-OCH3对MAPK或Raf-1激酶活性没有直接影响。还建立了ET18-OCH3积累、细胞增殖抑制、Raf与膜的结合以及MAPK激活之间的直接相关性。这些结果表明,ET18-OCH3通过对Raf-1激活的影响来抑制MAPK级联反应,这可能是ET18-OCH3抑制细胞增殖的重要机制。