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下调鞘氨醇激酶-1用于癌症治疗。

Downregulating sphingosine kinase-1 for cancer therapy.

作者信息

Cuvillier Olivier

机构信息

Institut de Pharmacologie et de Biologie Structurale, CNRS UMR 5089, 205 route de Narbonne, 31077 Toulouse Cedex 4, France.

出版信息

Expert Opin Ther Targets. 2008 Aug;12(8):1009-20. doi: 10.1517/14728222.12.8.1009.

Abstract

BACKGROUND

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.

OBJECTIVE

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.

摘要

背景

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。

目的

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。

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