Evidence map›Paper›PMID 28878674›Full record

ReviewFrontiers in pharmacology2017

Sphingosine Kinases and Sphingosine 1-Phosphate Receptors: Signaling and Actions in the Cardiovascular System.

Alessandro Cannavo, Daniela Liccardo, Klara Komici, Graziamaria Corbi, Claudio de Lucia, Grazia D Femminella, Andrea Elia, Leonardo Bencivenga, Nicola Ferrara, Walter J Koch and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
4.3field-weighted citation impact, top 5% 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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 102 citations in OpenAlex.

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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

12 authors at 6 institutions in 3 countries.

Alessandro CannavoLewis Katz School of Medicine, Center for Translational Medicine, Temple University, PhiladelphiaPA, United States.
Daniela LiccardoLewis Katz School of Medicine, Center for Translational Medicine, Temple University, PhiladelphiaPA, United States.
Klara KomiciDepartment of Translational Medical Sciences, University of Naples Federico IINaples, Italy.
Graziamaria CorbiDepartment of Medicine and Health Science, University of MoliseCampobasso, Italy.
Claudio de LuciaLewis Katz School of Medicine, Center for Translational Medicine, Temple University, PhiladelphiaPA, United States.
Grazia D FemminellaImperial College LondonLondon, United Kingdom.
Andrea EliaIstituti Clinici Scientifici Maugeri SpA Società Benefit, Telese Terme Institute (BN)Telese, Italy.
Leonardo BencivengaDepartment of Translational Medical Sciences, University of Naples Federico IINaples, Italy.
Nicola FerraraDepartment of Translational Medical Sciences, University of Naples Federico IINaples, Italy.
Walter J KochLewis Katz School of Medicine, Center for Translational Medicine, Temple University, PhiladelphiaPA, United States.
Nazareno PaolocciDivision of Cardiology, Johns Hopkins University Medical Institutions, BaltimoreMD, United States.
Giuseppe RengoDepartment of Translational Medical Sciences, University of Naples Federico IINaples, Italy.
University of Naples Federico II · ITTemple University · USIstituti Clinici Scientifici Maugeri · ITImperial College London · GBUniversity of Molise · ITUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sphingosine kinases 1 and 2 (SphK1 and 2) catalyze the phosphorylation of the lipid, sphingosine, generating the signal transmitter, sphingosine 1-phosphate (S1P). The activation of such kinases and the subsequent S1P generation and secretion in the blood serum of mammals represent a major checkpoint in many cellular signaling cascades. In fact, activating the SphK/S1P system is critical for cell motility and proliferation, cytoskeletal organization, cell growth, survival, and response to stress. In the cardiovascular system, the physiological effects of S1P intervene through the binding and activation of a family of five highly selective G protein-coupled receptors, called S1PR

Indexed as

cardiovascularfingolimodgene-therapyG protein-coupled receptorsheart failuresphingosine 1-phosphatesphingosine kinase

Identifiers

PMID28878674
PMCPMC5572949
OpenAlexW2746133014

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.