Evidence map›Paper›PMID 27656050›Full record

ReviewMediators of inflammation

Sphingolipids as Mediators in the Crosstalk between Microbiota and Intestinal Cells: Implications for Inflammatory Bowel Disease.

Phillips-Farfán Bryan, Carvajal Karla, Medina-Torres Edgar Alejandro, Espinosa-Padilla Sara Elva, Fabrias Gemma, Camacho Luz

Erratum issuedOpen access · goldAbstract readReview
In one paragraph

Review in Mediators of inflammation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

33 citing papers in PubMed, 51 citations in OpenAlex.

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  10. The diverse roles of sphingolipids in inflammatory bowel disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Phillips-Farfán BryanLaboratorio de Nutrición Experimental, Instituto Nacional de Pediatría, 04530 Ciudad de México, Mexico.
Carvajal KarlaLaboratorio de Nutrición Experimental, Instituto Nacional de Pediatría, 04530 Ciudad de México, Mexico.ORCID 0000-0002-5522-3266
Medina-Torres Edgar AlejandroUnidad de Investigación en Inmunodeficiencias, Instituto Nacional de Pediatría, 04530 Ciudad de México, Mexico.
Espinosa-Padilla Sara ElvaUnidad de Investigación en Inmunodeficiencias, Instituto Nacional de Pediatría, 04530 Ciudad de México, Mexico.
Fabrias GemmaResearch Unit on Bioactive Molecules, Department of Biomedicinal Chemistry, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), 08034 Barcelona, Spain.
Camacho LuzLaboratorio de Nutrición Experimental, Instituto Nacional de Pediatría, 04530 Ciudad de México, Mexico.ORCID 0000-0002-9864-3738
Instituto Nacional de Pediatria · MXInstitute of Advanced Chemistry of Catalonia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) describes different illnesses characterized by chronic inflammation of the gastrointestinal tract. Although the pathogenic mechanisms leading to IBD are poorly understood, immune system disturbances likely underlie its development. Sphingolipids (SLs) have been identified as important players and promising therapeutic targets to control inflammation in IBD. Interestingly, it seems that microorganisms of the normal gut microbiota and probiotics are involved in sphingolipid function. However, there is a great need to investigate the role of SLs as intermediates in the crosstalk between intestinal immunity and microorganisms. This review focuses on recent investigations that describe some mechanisms involved in the regulation of cytokine profiles by SLs. We also describe the importance of gut microbiota in providing signaling molecules that favor the communication between resident bacteria and intestinal cells. This, in turn, modulates the immune response in the bowel and likely in other peripheral organs. The potential of SLs and gut microbiota as targets or therapeutic agents for IBD is also discussed.

Identifiers

PMID27656050
PMCPMC5021499
OpenAlexW2507561280

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.