In this article, ceramide signaling will be reviewed in light of 'systems interface biology': as an interconnection of sphingolipid metabolism, membrane biophysics and cell signaling.
First-pass extracted concept
ceramide signaling
Evidence Snippets
Supporting Sources
Linked Claims
Ceramide/sphingomyelin- and ceramide/sphingosine-1-phosphate-interdependent signaling pathways are significant for regulation of cell polarity, apoptosis, and/or proliferation.
Ceramide/sphingomyelin and ceramide/sphingosine-1-phosphate-interdependent cell-signaling pathways are significant for the regulation of cell polarity, apoptosis and/or proliferation
Ceramide signaling can be framed as an interconnection of sphingolipid metabolism, membrane biophysics, and cell signaling.
ceramide signaling will be reviewed in light of 'systems interface biology': as an interconnection of sphingolipid metabolism, membrane biophysics and cell signaling
Previous work has mainly focused on ceramide as an apoptosis inducer.
Most of the previous work on the sphingolipid ceramide has been devoted to its function as an apoptosis inducer.
Recent studies have shown that in stem cells ceramide has additional nonapoptotic functions.
Recent studies, however, have shown that in stem cells, ceramide has additional nonapoptotic functions.
The review focuses on metabolic interconversion of ceramide with sphingomyelin and sphingosine-1-phosphate.
The focus will be on the metabolic interconversion of ceramide and sphingomyelin or sphingosine-1-phosphate.
Ceramide/sphingomyelin and ceramide/sphingosine-1-phosphate signaling pathways are presented as novel pharmacologic targets in cancer and stem cells.
Ceramide/sphingomyelin and ceramide/sphingosine-1-phosphate-interdependent cell-signaling pathways are significant for the regulation of cell polarity, apoptosis and/or proliferation, and as novel pharmacologic targets in cancer and stem cells.