Evidence map›Paper›PMID 17669501›Full record

ReviewPharmacology & therapeutics2007

Sphingosine-1-phosphate in allergic responses, asthma and anaphylaxis.

Carole A Oskeritzian, Sheldon Milstien, Sarah Spiegel

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 90 citations in OpenAlex.

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  16. Orosomucoid-like protein 3, rhinovirus and asthma.World journal of critical care medicine · 2021
    Review
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  18. Article
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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.

Carole A OskeritzianDepartment of Biochemistry and Molecular Biology, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA. coskerit@vcu.edu
Sheldon Milstien
Sarah Spiegel
Virginia Commonwealth University · US

Funding

Sphingosine Kinases in Cancer Cell SignalingR01CA061774 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SPIEGEL, SARAH · 1994 to 2015
$3.8M
Targeting sphingosine kinases in FceRI-mediated allergic responsesR01AI050094 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI SPIEGEL, SARAH · 2002 to 2012
$2.9M
Sphingosine-1-Phosphate, A Novel Mediator of Human Skin Mass Cell FunctionsK01AR053186 · NIAMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI OSKERITZIAN, CAROLE A · 2006 to 2010
$522k
Sphingolipid Signaling and Pteridine BiosynthesisZ01MH001039 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MILSTIEN, SHELDON · 1985 to 2008
$469k
Intramural NIH HHSNCI NIH HHS R01 CA061774NIAID NIH HHS R01 AI050094NIAID NIH HHS R01 AI50094NIAMS NIH HHS K01 AR053186
6 · The paper itself

Abstract

Sphingosine-1-phosphate (S1P) is a bioactive sphingolipid metabolite involved in many cellular processes, acting not only as an extracellular ligand to its specific G protein-coupled receptors, but also as a putative intracellular messenger with yet unidentified targets. Mast cells are tissue-dwelling pivotal early effectors of allergic responses, which produce and secrete S1P that can bind to its receptors present on mast cells to influence their activation and functions. In this review, we will first discuss the current knowledge of S1P production by two isozymes of sphingosine kinase (SphK). Mechanisms of SphK activation will be discussed, with an emphasis on experimental approaches developed to study their differential activation and biological roles in the context of mast cells. The relevance of mast cells in the etiology of allergic disorders, asthma and anaphylaxis is well established. In this review, this concept will be revisited, focusing on the contribution of S1P production and secretion to the symptoms associated with dysregulated inflammatory responses. To conclude, counteracting the proinflammatory effects of S1P could be envisioned as a therapeutic strategy to treat allergic disorders, exacerbated airway inflammation, and anaphylactic reactions, and various options will be discussed, such as the development of pharmacological tools to inhibit SphKs, S1P neutralizing monoclonal antibody, and S1P receptor antagonists.

Indexed as

AnaphylaxisAnimalsAntibodies, MonoclonalAsthmaDrug Delivery SystemsHumansHypersensitivityLysophospholipidsMast CellsReceptors, LysosphingolipidSphingosineAntibodies, MonoclonalLysophospholipidsReceptors, LysosphingolipidSphingosinesphingosine 1-phosphate

Identifiers

PMID17669501
PMCPMC2082108
OpenAlexW1985668252

What OpenQuestion holds

Textmetadata
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.