Cuvillier Olivier
Institut de Pharmacologie et de Biologie Structurale, CNRS UMR 5089, 205 route de Narbonne, 31077 Toulouse Cedex 4, France.
Expert Opin Ther Targets. 2008 Aug;12(8):1009-20. doi: 10.1517/14728222.12.8.1009.
The sphingolipids ceramide and sphingosine 1-phosphate (S1P) are key regulators of cell death and proliferation. The subtle balance between their intracellular levels is governed mainly by sphingosine kinase-1, which produces the pro-survival S1P. Sphingosine kinase-1 is an oncogene; is overexpressed in many tumors; protects cancer cells from apoptosis in vitro and in vivo; and its activity is decreased by anticancer therapies. Hence, sphingosine kinase-1 appears to be a target of interest for therapeutic manipulation.
This review considers recent developments regarding the involvement of sphingosine kinase-1 as a therapeutic target for cancer, and describes the pharmacological tools currently available.
RESULTS/CONCLUSION: The studies described provide strong evidence that strategies to kill cancer cells via sphingosine kinase-1 inhibition are valid and could have a favorable therapeutic index.
鞘脂类神经酰胺和1-磷酸鞘氨醇(S1P)是细胞死亡和增殖的关键调节因子。它们细胞内水平的微妙平衡主要由产生促生存S1P的鞘氨醇激酶-1调控。鞘氨醇激酶-1是一种癌基因;在许多肿瘤中过度表达;在体外和体内保护癌细胞免于凋亡;并且其活性可被抗癌治疗降低。因此,鞘氨醇激酶-1似乎是一个具有治疗操控价值的靶点。
本综述探讨了鞘氨醇激酶-1作为癌症治疗靶点的最新进展,并描述了目前可用的药理学工具。
结果/结论:所描述的研究提供了强有力的证据,表明通过抑制鞘氨醇激酶-1来杀死癌细胞的策略是有效的,并且可能具有良好的治疗指数。