Evidence map›Paper›PMID 25923252›Full record

ReviewCritical reviews in biochemistry and molecular biology2015

Sphingosine-1-phosphate metabolism: A structural perspective.

Michael J Pulkoski-Gross, Jane C Donaldson, Lina M Obeid

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in biochemistry and molecular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Molecular mechanisms of regulation of sphingosine kinase 1.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2018
    Review
  11. Review
  12. Article
  13. "Dicing and Splicing" Sphingosine Kinase and Relevance to Cancer.International journal of molecular sciences · 2017
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
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

3 authors at 1 institution in 1 country.

Michael J Pulkoski-Grossa Department of Pharmacological Sciences and.
Jane C Donaldsonb Department of Medicine , Stony Brook University , Stony Brook , NY , USA .
Lina M Obeidb Department of Medicine , Stony Brook University , Stony Brook , NY , USA .
Stony Brook University · US

Funding

Sphingolipids in Cancer Therapy and AngiogenesisP01CA097132 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI YUSUF AWNI HANNUN · 2003 to 2026
$30.8M
Training Program in Pharmacological SciencesT32GM007518 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI GARCIA-DIAZ, MIGUEL · 1985 to 2021
$5.4M
Role and Regulation of Ceramide Synthases in ApoptosisR01GM097741 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI LUBERTO, CHIARA · 2011 to 2019
$3.5M
Regulation and Role of Ceramidase in InflammationI01BX000156 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI OBEID, LINA M · 2009 to 2017
–
BLRD VA I01 BX000156NCI NIH HHS P01 CA097132NCI NIH HHS P01CA097132NIGMS NIH HHS GM097741NIGMS NIH HHS R01 GM097741NIGMS NIH HHS T32 GM007518NIGMS NIH HHS T32GM007518
6 · The paper itself

Abstract

Sphingolipids represent an important class of bioactive signaling lipids which have key roles in numerous cellular processes. Over the last few decades, the levels of bioactive sphingolipids and/or their metabolizing enzymes have been realized to be important factors involved in disease development and progression, most notably in cancer. Targeting sphingolipid-metabolizing enzymes in disease states has been the focus of many studies and has resulted in a number of pharmacological inhibitors, with some making it into the clinic as therapeutics. In order to better understand the regulation of sphingolipid-metabolizing enzymes as well as to develop much more potent and specific inhibitors, the field of sphingolipids has recently taken a turn toward structural biology. The last decade has seen the structural determination of a number of sphingolipid enzymes and effector proteins. In these terms, one of the most complete arms of the sphingolipid pathway is the sphingosine-1-phosphate (S1P) arm. The structures of proteins involved in the function and regulation of S1P are being used to investigate further the regulation of said proteins as well as in the design and development of inhibitors as potential therapeutics.

Indexed as

Models, MolecularSecond Messenger SystemsAldehyde-LyasesAnimalsBinding SitesBiological TransportEnzyme InhibitorsHumansLigandsLysophospholipidsMembrane Transport ModulatorsMolecular ConformationPhosphotransferases (Alcohol Group Acceptor)Receptors, LysosphingolipidSphingosineSphingosine-1-Phosphate ReceptorsAldehyde-LyasesEnzyme InhibitorsLigandsLysophospholipidsMembrane Transport ModulatorsPhosphotransferases (Alcohol Group Acceptor)Receptors, LysosphingolipidS1PR1 protein, humanSphingosinesphingosine 1-phosphatesphingosine 1-phosphate lyase (aldolase)Sphingosine-1-Phosphate ReceptorsSphingosine Kinasesphingosine kinase 2, humanSphingolipid metabolismsphingosine-1-phosphatesphingosine-1-phosphate receptorssphingosine kinasesstructural biology

Identifiers

PMID25923252
PMCPMC5476942
OpenAlexW1975094886

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.