An oncogenic role of sphingosine kinase

被引:361
作者
Xia, P [1 ]
Gamble, JR [1 ]
Wang, LJ [1 ]
Pitson, SM [1 ]
Moretti, PAB [1 ]
Wattenberg, BW [1 ]
D'Andrea, RJ [1 ]
Vadas, MA [1 ]
机构
[1] Univ Adelaide, Hanson Ctr Canc Res, Div Human Immunol, Inst Med & Vet Sci, Adelaide, SA 5000, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0960-9822(00)00834-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sphingosine kinase (SphK) is a highly conserved lipid kinase that phosphorylates sphingosine to form sphingosine-1-phosphate (S1P). S1P/SphK has been implicated as a signalling pathway to regulate diverse cellular functions [1-3], including cell growth, proliferation and survival [4-8]. We report that cells overexpressing SphK have increased enzymatic activity and acquire the transformed phenotype, as determined by focus formation, colony growth in soft agar and the ability to form tumours in NOD/SCID mice. This is the first demonstration that a wild-type lipid kinase gene acts as an oncogene. Using a chemical inhibitor of SphK, or an SphK mutant that inhibits enzyme activation, we found that SphK activity is involved in oncogenic H-Ras-mediated transformation, suggesting a novel signalling pathway for Ras activation. The findings not only point to a new signalling pathway in transformation but also to the potential of SphK inhibitors in cancer therapy.
引用
收藏
页码:1527 / 1530
页数:4
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