Literature DB >> 7782925

Role of dietary sphingolipids and inhibitors of sphingolipid metabolism in cancer and other diseases.

A H Merrill1, E M Schmelz, E Wang, J J Schroeder, D L Dillehay, R T Riley.   

Abstract

Sphingolipids are found in all eukaryotic and some prokaryotic organisms and participate in the regulation of cell growth, differentiation, and diverse cell functions including cell-cell communication, cell-substratum interactions and intracellular signal transduction. Nonetheless, the field of nutrition has given scant attention to these compounds so that little is known about the following fundamental questions: What is the fate of sphingolipids that are consumed in food? Does consumption of dietary sphingolipids affect the behavior of cells in the gastrointestinal tract or other organs? How do other factors in the diet affect sphingolipid metabolism? Several recent findings underscore the importance of these questions, for examples: 1) Sphingolipids are digested throughout the GI tract to ceramide and sphingosine, which are highly bioactive compounds that affect cellular regulatory pathways; 2) addition of sphingomyelin to a standard AIN diet (which is essentially devoid of sphingolipids) reduces the appearance of aberrant colonic crypts, and perhaps the number of tumors, in mice treated with a colon carcinogen; and 3) an enzyme of sphingolipid metabolism has been discovered to be the target of a class of toxic and carcinogenic mycotoxins called fumonisins. Given these recent findings, it is possible that some of the confusion that has arisen regarding the relationships between dietary fat and disease might be due to the lack of consideration of the sphingolipids that are also present.

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Year:  1995        PMID: 7782925     DOI: 10.1093/jn/125.suppl_6.1677S

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  12 in total

1.  Screening of fungal species for fumonisin production and fumonisin-like disruption of sphingolipid biosynthesis.

Authors:  W P Norred; C W Bacon; R T Riley; K A Voss; F I Meredith
Journal:  Mycopathologia       Date:  1999       Impact factor: 2.574

2.  Oral glucosylceramide reduces 2,4-dinitrofluorobenzene induced inflammatory response in mice by reducing TNF-alpha levels and leukocyte infiltration.

Authors:  Jingjing Duan; Tatsuya Sugawara; Shota Sakai; Kazuhiko Aida; Takashi Hirata
Journal:  Lipids       Date:  2011-01-11       Impact factor: 1.880

3.  Conversion of dihydroceramide into ceramide: involvement of a desaturase.

Authors:  L Geeraert; G P Mannaerts; P P van Veldhoven
Journal:  Biochem J       Date:  1997-10-01       Impact factor: 3.857

4.  Effects of ursodeoxycholate and other bile salts on levels of rat intestinal alkaline sphingomyelinase: a potential implication in tumorigenesis.

Authors:  R D Duan; Y Cheng; H D Tauschel; A Nilsson
Journal:  Dig Dis Sci       Date:  1998-01       Impact factor: 3.199

5.  Functional studies of human intestinal alkaline sphingomyelinase by deglycosylation and mutagenesis.

Authors:  Jun Wu; Gert H Hansen; Ake Nilsson; Rui-Dong Duan
Journal:  Biochem J       Date:  2005-02-15       Impact factor: 3.857

Review 6.  Sphingolipid signaling in metabolic disorders.

Authors:  Timothy Hla; Andrew J Dannenberg
Journal:  Cell Metab       Date:  2012-09-13       Impact factor: 27.287

7.  Distribution of alkaline sphingomyelinase activity in human beings and animals. Tissue and species differences.

Authors:  R D Duan; E Hertervig; L Nyberg; T Hauge; B Sternby; J Lillienau; A Farooqi; A Nilsson
Journal:  Dig Dis Sci       Date:  1996-09       Impact factor: 3.199

8.  Sphingosine-1-phosphate stimulates human Caco-2 intestinal epithelial proliferation via p38 activation and activates ERK by an independent mechanism.

Authors:  Vijayalakshmi Thamilselvan; Wei Li; Bauer E Sumpio; Marc D Basson
Journal:  In Vitro Cell Dev Biol Anim       Date:  2002-04       Impact factor: 2.416

9.  Application of Comparative Lipidomics to Elucidate Postprandial Metabolic Excursions Following Dairy Milk Ingestion in Individuals with Prediabetes.

Authors:  Li Chen; Shiqi Zhang; Xiaowei Sun; Joshua D McDonald; Richard S Bruno; Jiangjiang Zhu
Journal:  J Proteome Res       Date:  2021-03-15       Impact factor: 4.466

10.  Identification of aberrant forms of alkaline sphingomyelinase (NPP7) associated with human liver tumorigenesis.

Authors:  Y Cheng; J Wu; E Hertervig; S Lindgren; D Duan; A Nilsson; R-D Duan
Journal:  Br J Cancer       Date:  2007-10-09       Impact factor: 7.640

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