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Sphingolipid pathway enzymes modulate cell fate and immune responses. Immunotherapy 2017 Nov;9(14):1185-1198

Date

10/27/2017

Pubmed ID

29067886

DOI

10.2217/imt-2017-0089

Scopus ID

2-s2.0-85032440636 (requires institutional sign-in at Scopus site)   25 Citations

Abstract

Sphingolipids (SLs) are a class of essential, bioactive lipids. The SL family includes over 4000 distinct molecules, characterized by their sphingoid base (long-chain aliphatic amine) backbone. SLs are key components of cell membranes, yet their roles go well beyond structure. SLs are involved in many cellular processes including cell differentiation, apoptosis, growth arrest and senescence. As cancer cells routinely display increased growth properties and escape from cell death, it has been suggested that enzymes involved in SL synthesis or catabolism may be altered in cancer cells. In this review, we discuss the role of SL pathway enzymes in cancer, and in acquired resistance to therapy. The use of inhibitors and gene silencing approaches targeting these SL pathways is also explored. Finally, we elaborate on the role of SL pathway enzymes in the tumor microenvironment and their effect on immune cell function.

Author List

Molino S, Tate E, McKillop WM, Medin JA

Author

Jeffrey A. Medin PhD Professor in the Pediatrics department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Animals
Apoptosis
Cell Cycle
Cell Differentiation
Drug Resistance, Neoplasm
Humans
Immunity
Lipid Metabolism
Molecular Targeted Therapy
Neoplasms
Signal Transduction
Sphingolipids