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基于1-磷酸鞘氨醇信号通路的药物研发

[The drug development based on sphingosine-1-phosphate signaling pathway].

作者信息

Bai Jie, Hu Jin-ping

出版信息

Yao Xue Xue Bao. 2016 Dec;51(12):1822-8.

Abstract

Sphingosine-1-phosphate (S1P), a bioactive sphingolipid produced by the metabolism of sphingomyelin, regulates cell proliferation, migration, survival and cell-cell contacts. The sphingosine-1- phosphate signaling pathway can regulate the trafficking of lymphocyte, angiogenesis, the progress of cancer and many other cellular functions. The formation of S1P is catalyzed by sphingosine kinases (SPHK), and degraded by lyases(S1PL), therefore S1P level is subject to a dynamic balance in the physiological environment. S1P can act as a second messenger or couple with S1P receptors (S1PR) to exert effects. The targets in the S1P signaling pathway have received considerable attention. Here we review the physiological function and drug development of S1P signaling pathway.

摘要

鞘氨醇-1-磷酸(S1P)是一种由鞘磷脂代谢产生的生物活性鞘脂,可调节细胞增殖、迁移、存活及细胞间接触。鞘氨醇-1-磷酸信号通路可调节淋巴细胞运输、血管生成、癌症进展及许多其他细胞功能。S1P的形成由鞘氨醇激酶(SPHK)催化,并由裂解酶(S1PL)降解,因此在生理环境中S1P水平处于动态平衡。S1P可作为第二信使或与S1P受体(S1PR)结合发挥作用。S1P信号通路中的靶点已受到广泛关注。在此,我们综述S1P信号通路的生理功能及药物研发情况。

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