Literature DB >> 8280742

Sphingolipid breakdown products: anti-proliferative and tumor-suppressor lipids.

Y A Hannun1, C M Linardic.   

Abstract

The sphingolipids are a family of lipids found ubiquitously in eukaryotic cell membranes. Within the last decade sphingolipids have emerged as active participants in the regulation of cell growth, differentiation, transformation, and cell-cell contact. A prototypic sphingolipid signalling pathway is the 'sphingomyelin cycle,' in which membrane sphingomyelin is hydrolyzed in response to extracellular stimuli, generating the putative second messenger ceramide. Ceramide, in turn, is thought to propagate the signal into the cell interior by the activation of a phosphatase. It is likely that other sphingolipids are components of similar signalling cycles, generating a variety of lipid messengers which participate in as yet undefined pathways. Sphingosine, for example, is a potential breakdown product of all sphingolipids, and is well-known for its pharmacologic inhibition of protein kinase C. However, it is becoming apparent that sphingosine is active in multiple signalling cascades that are independent of protein kinase C, including effects on fibroblast cell growth and the regulation of the retinoblastoma tumor suppressor protein. Similarly, lyso-sphingolipids, while comprising only a minor fraction of the cell's total sphingolipids, are turning out to have biological effects which warrant their investigation as potential signalling molecules. A distinguishing characteristic of sphingolipid breakdown products is their apparent participation in anti-proliferative pathways of cell regulation. Thus, sphingolipid breakdown products can be found to play roles in growth inhibition, induction of differentiation, and programmed cell death. In coordination with other cellular signal transduction pathways, the sphingolipid breakdown products may be the harnesses on cell growth and may also contribute to the suppression of oncogenesis.

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Year:  1993        PMID: 8280742     DOI: 10.1016/0304-4157(93)90001-5

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  55 in total

1.  Activation of neutral sphingomyelinase in human neutrophils by polyunsaturated fatty acids.

Authors:  B S Robinson; C S Hii; A Poulos; A Ferrante
Journal:  Immunology       Date:  1997-06       Impact factor: 7.397

Review 2.  Rafts as missing link between multidrug resistance and sphingolipid metabolism.

Authors:  J W J Hinrichs; K Klappe; J W Kok
Journal:  J Membr Biol       Date:  2005-01       Impact factor: 1.843

3.  Multiple actions of doxorubicin on the sphingolipid network revealed by flux analysis.

Authors:  Justin M Snider; Magali Trayssac; Christopher J Clarke; Nicholas Schwartz; Ashley J Snider; Lina M Obeid; Chiara Luberto; Yusuf A Hannun
Journal:  J Lipid Res       Date:  2018-12-20       Impact factor: 5.922

4.  p53-dependent ceramide response to genotoxic stress.

Authors:  G S Dbaibo; M Y Pushkareva; R A Rachid; N Alter; M J Smyth; L M Obeid; Y A Hannun
Journal:  J Clin Invest       Date:  1998-07-15       Impact factor: 14.808

Review 5.  Apoptosis -- the story so far....

Authors:  A Samali; A M Gorman; T G Cotter
Journal:  Experientia       Date:  1996-10-31

6.  Activation of caspase-3-like proteases in apoptosis induced by sphingosine and other long-chain bases in Hep3B hepatoma cells.

Authors:  W C Hung; H C Chang; L Y Chuang
Journal:  Biochem J       Date:  1999-02-15       Impact factor: 3.857

Review 7.  Mechanisms and functional features of polarized membrane traffic in epithelial and hepatic cells.

Authors:  M M Zegers; D Hoekstra
Journal:  Biochem J       Date:  1998-12-01       Impact factor: 3.857

Review 8.  Phytosterols in the prevention of human pathologies.

Authors:  H Tapiero; D M Townsend; K D Tew
Journal:  Biomed Pharmacother       Date:  2003-10       Impact factor: 6.529

9.  Enzymic glycosphingolipid synthesis on polymer supports. III. Synthesis of GM3, its analog [NeuNAcalpha(2-3)Galbeta(1-4)Glcbeta(1-3)Cer] and their lyso-derivatives.

Authors:  U Zehavi; A Tuchinsky
Journal:  Glycoconj J       Date:  1998-07       Impact factor: 2.916

10.  Reduction in alkaline sphingomyelinase in colorectal tumorigenesis is not related to the APC gene mutation.

Authors:  Erik Hertervig; Ake Nilsson; Mef Nilbert; Rui-Dong Duan
Journal:  Int J Colorectal Dis       Date:  2003-03-04       Impact factor: 2.571

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