Evidence map›Paper›PMID 28362332›Full record

ReviewInternational journal of molecular sciences2017

Sphingosine-1-Phosphate Metabolism and Its Role in the Development of Inflammatory Bowel Disease.

Tomasz Wollny, Marzena Wątek, Bonita Durnaś, Katarzyna Niemirowicz, Ewelina Piktel, Małgorzata Żendzian-Piotrowska, Stanisław Góźdź, Robert Bucki

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

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  17. Sphingosine-1-Phosphate Enhances αInternational journal of molecular sciences · 2019
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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

8 authors at 3 institutions in 1 country.

Tomasz WollnyHoly Cross Oncology Center of Kielce, Artwińskiego 3, 25-734 Kielce, Poland. tomwollny@gmail.com.
Marzena WątekHoly Cross Oncology Center of Kielce, Artwińskiego 3, 25-734 Kielce, Poland. marzena.watek@wp.pl.
Bonita DurnaśDepartment of Microbiology and Immunology, The Faculty of Health Sciences of the Jan Kochanowski University in Kielce, Aleja IX Wieków Kielc, 25-317 Kielce, Poland. bonita.durnas@onkol.kielce.pl.
Katarzyna NiemirowiczDepartment of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, 15-222 Białystok, Poland. katia146@wp.pl.
Ewelina PiktelDepartment of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, 15-222 Białystok, Poland. ewelina.piktel@wp.pl.
Małgorzata Żendzian-PiotrowskaDepartment of Hygiene, Epidemiology and Ergonomics, Medical University of Białystok, 15-230 Białystok, Poland. mzpiotrowska@gmail.com.
Stanisław GóźdźHoly Cross Oncology Center of Kielce, Artwińskiego 3, 25-734 Kielce, Poland. stanislaw.gozdz@onkol.kielce.pl.
Robert BuckiDepartment of Microbiological and Nanobiomedical Engineering, Medical University of Białystok, 15-222 Białystok, Poland. buckirobert@gmail.com.
Medical University of Białystok · PLJan Kochanowski University · PLHoly Cross University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beyond their role as structural molecules, sphingolipids are involved in many important cellular processes including cell proliferation, apoptosis, inflammation, and migration. Altered sphingolipid metabolism is observed in many pathological conditions including gastrointestinal diseases. Inflammatory bowel disease (IBD) represents a state of complex, unpredictable, and destructive inflammation of unknown origin within the gastrointestinal tract. The mechanisms explaining the pathophysiology of IBD involve signal transduction pathways regulating gastro-intestinal system's immunity. Progressive intestinal tissue destruction observed in chronic inflammation may be associated with an increased risk of colon cancer. Sphingosine-1-phosphate (S1P), a sphingolipid metabolite, functions as a cofactor in inflammatory signaling and becomes a target in the treatment of IBD, which might prevent its conversion to cancer. This paper summarizes new findings indicating the impact of (S1P) on IBD development and IBD-associated carcinogenesis.

Indexed as

Signal TransductionAnimalsCell Transformation, NeoplasticColonic NeoplasmsDisease ProgressionHumansInflammatory Bowel DiseasesLysophospholipidsModels, BiologicalRisk FactorsSphingosineLysophospholipidsSphingosinesphingosine 1-phosphatecancerinflammatory bowel diseasesphingosine-1-phosphate

Identifiers

PMID28362332
PMCPMC5412326
OpenAlexW2598077740

What OpenQuestion 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 OpenQuestion graph.