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鞘氨醇-1-磷酸与癌症

Sphingosine 1-phosphate and cancer.

作者信息

Pyne Nigel J, El Buri Ashref, Adams David R, Pyne Susan

机构信息

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161 Cathedral St, Glasgow, G4 0RE, Scotland, UK.

Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161 Cathedral St, Glasgow, G4 0RE, Scotland, UK.

出版信息

Adv Biol Regul. 2018 May;68:97-106. doi: 10.1016/j.jbior.2017.09.006. Epub 2017 Sep 15.

Abstract

The bioactive lipid, sphingosine 1-phosphate (S1P) is produced by phosphorylation of sphingosine and this is catalysed by two sphingosine kinase isoforms (SK1 and SK2). Here we discuss structural functional aspects of SK1 (which is a dimeric quaternary enzyme) that relate to coordinated coupling of membrane association with phosphorylation of Ser225 in the 'so-called' R-loop, catalytic activity and protein-protein interactions (e.g. TRAF2, PP2A and G). S1P formed by SK1 at the plasma-membrane is released from cells via S1P transporters to act on S1P receptors to promote tumorigenesis. We discuss here an additional novel mechanism that can operate between cancer cells and fibroblasts and which involves the release of the S1P receptor, S1P in exosomes from breast cancer cells that regulates ERK-1/2 signalling in fibroblasts. This novel mechanism of signalling might provide an explanation for the role of S1P in promoting metastasis of cancer cells and which is dependent on the micro-environmental niche.

摘要

生物活性脂质鞘氨醇-1-磷酸(S1P)由鞘氨醇磷酸化产生,这一过程由两种鞘氨醇激酶同工型(SK1和SK2)催化。在此,我们讨论SK1(一种二聚体四级酶)的结构功能方面,这些方面涉及膜结合与“所谓的”R环中Ser225磷酸化的协同偶联、催化活性以及蛋白质-蛋白质相互作用(如TRAF2、PP2A和G)。SK1在质膜上形成的S1P通过S1P转运蛋白从细胞中释放出来,作用于S1P受体以促进肿瘤发生。我们在此讨论一种可在癌细胞和成纤维细胞之间起作用的额外新机制,该机制涉及乳腺癌细胞外泌体中S1P受体S1P的释放,其可调节成纤维细胞中的ERK-1/2信号传导。这种新的信号传导机制可能为S1P在促进癌细胞转移中的作用提供解释,而这一作用取决于微环境生态位。

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