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

机译:1-O-十八烷基-2-O-甲基-甘油磷酸胆碱通过培养的MCF-7细胞中的MAPK级联抑制生长信号的转导。

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摘要

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.
机译:1-O-十八烷基-2-O-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质,其作用机理尚未确定。我们假设,由于ET18-OCH3影响多种细胞,其作用机制可能涉及抑制普遍广泛使用的转导生长信号的途径,如促分裂原活化的蛋白激酶(MAPK)级联。为了测试这一点,我们建立了静止的MCF-7细胞吸收足够量的ET18-OCH3的条件,从而抑制了添加生长培养基后的细胞增殖,并研究了在这些条件下MAPK级联组件的激活。 ET18-OCH3抑制了MAPK的持续磷酸化,从而导致血清或EGF刺激的细胞中MAPK活化的幅度和持续时间降低。 ET18-OCH3对EGF与其受体的结合,其激活或p21ras激活没有影响。但是,观察到干扰Raf-1与膜的结合,并导致ET18-OCH3处理的细胞膜的Raf-1激酶活性降低。 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与膜结合以及MAPK激活之间的直接关联。这些结果表明,ET18-OCH3对Raf-1激活的影响可能会抑制ET18-OCH3的MAPK级联反应,这可能是ET18-OCH3抑制细胞增殖的重要机制。

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