When the Sphingosine Kinase 1/Sphingosine 1-Phosphate Pathway Meets Hypoxia Signaling: New Targets for Cancer Therapy

被引:62
|
作者
Ader, Isabelle [1 ,2 ]
Malavaud, Bernard [1 ,2 ,3 ]
Cuvillier, Olivier [1 ,2 ]
机构
[1] CNRS, UMR 5089, Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
[2] Univ Toulouse, UPS, IPBS, Toulouse, France
[3] CHU Toulouse, Hop Rangueil, Toulouse, France
关键词
INDUCIBLE-FACTOR; 1-ALPHA; CELL; EXPRESSION; HYPOXIA-INDUCIBLE-FACTOR-1-ALPHA; SPHINGOSINE-1-PHOSPHATE; NORMALIZATION; OXYGENATION; ACTIVATION; FACTOR-1; HIF-1;
D O I
10.1158/0008-5472.CAN-09-0389
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The reduction in the normal level of tissue oxygen tension or hypoxia is a characteristic of solid tumors that triggers the activation of signaling pathways promoting neovascularization, metastasis, increased tumor growth, and resistance to treatments. The activation of the transcription factor hypoxia-inducible factor 1 alpha (HIF-1 alpha) has been identified as the master mechanism of adaptation to hypoxia. In a recent study, we identified the sphingosine kinase 1/sphingosine 1-phosphate (SphK1/S1P) pathway, which elicits various cellular processes including cell proliferation, cell survival, or angiogenesis, as a new modulator of HIF-1 alpha activity under hypoxic conditions. Here, we consider how the SphK1/S1P signaling pathway could represent a very important target for therapeutic intervention in cancer. [Cancer Res 2009;69(9):3723-6]
引用
收藏
页码:3723 / 3726
页数:4
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