Evidence map›Paper›PMID 23579449›Full record

ReviewHandbook of experimental pharmacology2013

Sphingolipid metabolism and neutral sphingomyelinases.

Michael V Airola, Yusuf A Hannun

Abstract readReview
In one paragraph

Review in Handbook of experimental pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
18.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

102 citing papers in PubMed, 179 citations in OpenAlex.

  1. Article
  2. Sirtuin 1 Is Required for Optimal Mammarenavirus Multiplication.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Sphingosine-1-phosphate activates IJournal of molecular and cellular cardiology · 2026
    Article
  5. Review
  6. Article
  7. Molecular and Physiological Responses ofAntioxidants (Basel, Switzerland) · 2025
    Article
  8. Review
  9. Review
  10. Neutral sphingomyelinase 2: A promising drug target for CNS disease.Advances in pharmacology (San Diego, Calif.) · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

42 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Michael V AirolaDepartment of Medicine, Stony Brook University Cancer Center, Stony Brook University, Health Science Center, L-4, 178, Stony Brook, NY 11794, USA.
Yusuf A Hannun
Stony Brook University · US

Funding

Sphingomyelin Turnover and Cellular RegulationR37GM043825 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI HANNUN, YUSUF AWNI · 2007 to 2015
$3.7M
Regulation of Neutral Sphingomyelinase 2 by Inter-Domain InteractionsF32GM100679 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI AIROLA, MICHAEL VIRGIL · 2012 to 2014
$102k
NIGMS NIH HHS 1F32GM100679NIGMS NIH HHS F32 GM100679NIGMS NIH HHS R37 GM043825NIGMS NIH HHS R37GM43825
6 · The paper itself

Abstract

Sphingolipids are an important class of lipid molecules that play fundamental roles in our cells and body. Beyond a structural role, it is now clearly established that sphingolipids serve as bioactive signaling molecules to regulate diverse processes including inflammatory signaling, cell death, proliferation, and pain sensing. Sphingolipid metabolites have been implicated in the onset and progression of various diseases including cancer, lung disease, diabetes, and lysosomal storage disorders. Here we review sphingolipid metabolism to introduce basic concepts as well as emerging complexities in sphingolipid function gained from modern technological advances and detailed cell and animal studies. Furthermore, we discuss the family of neutral sphingomyelinases (N-SMases), which generate ceramide through the hydrolysis of sphingomyelin and are key enzymes in sphingolipid metabolism. Four mammalian N-SMase enzymes have now been identified. Most prominent is nSMase2 with established roles in bone mineralization, exosome formation, and cellular stress responses. Function for the other N-SMases has been more enigmatic and is an area of active investigation. The known properties and potential role(s) of each enzyme are discussed to help guide future studies.

Indexed as

AnimalsBone DevelopmentHumansSignal TransductionSphingolipidsSphingomyelin PhosphodiesteraseSphingolipidsSphingomyelin Phosphodiesterase

Identifiers

PMID23579449
PMCPMC4043343
OpenAlexW157208926

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.