Anticancer activity of FTY720: Phosphorylated FTY720 inhibits autotaxin, a metastasis-enhancing and angiogenic lysophospholipase D

被引:55
作者
van Meeteren, Laurens A. [1 ,2 ]
Brinkmann, Volker [3 ]
Saulnier-Blache, Jean Sebastien [4 ]
Lynch, Kevin R. [5 ]
Moolenaar, Wouter H. [1 ,2 ]
机构
[1] Netherlands Canc Inst, Div Cellular Biochem, NL-1066 Amsterdam, Netherlands
[2] Netherlands Canc Inst, Ctr Biomed Genet, NL-1066 Amsterdam, Netherlands
[3] Novartis Inst BioMed Res, Basel, Switzerland
[4] Dept Metab & Obes, INSERM U85812MR, Toulouse, France
[5] Univ Virginia, Dept Pharmacol, Charlottesville, VA 22908 USA
关键词
FTY720; autotaxin; lysophosphatidic acid; tumor progression;
D O I
10.1016/j.canlet.2008.02.052
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
FTY720 is an immunomodulator that is phosphorylated in vivo and inhibits lymphocyte mobilization by targeting sphingosine 1-phospate receptors. At doses higher than required for immunomodulation, FTY720 inhibits tumor progression through an unknown mechanism. Here we show that FTY720-phosphate is a competitive inhibitor (K(i)similar to 0.2 PM) of autotaxin (ATX or NPP2), a nucleotide phosphodiesterase/pyrophosphatase (NPP) that enhances metastasis and angiogenesis and acts as a lysophospholipase D to produce the lipid mediator lysophosphatidic acid (LPA). FTY720-phosphate did no affect the activity of NPPl, the closest relative of ATX, After oral administration in mice, FTY720 (3 mg/kg) significantly reduced plasma LPA levels. These results suggest that FTY720 may exert its anticancer effects, at least in part, by targeting the ATX-LPA axis. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:203 / 208
页数:6
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