Evidence map›Paper›PMID 31360579›Full record

ArticleLiver research (Beijing, China)2019

Sphingosine-1-phosphate signaling and the gut-liver axis in liver diseases.

Eric K Kwong, Huiping Zhou

Open access · goldAbstract read
In one paragraph

Article in Liver research (Beijing, China), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. The xenobiotic receptors PXR and CAR in liver physiology, an update.Biochimica et biophysica acta. Molecular basis of disease · 2021
    Review
  13. Bile Acid Signaling in Inflammatory Bowel Diseases.Digestive diseases and sciences · 2021
    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

2 authors at 2 institutions in 1 country.

Eric K KwongDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
Huiping ZhouDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA, USA.
Hunter Holmes McGuire VA Medical Center · USVirginia Commonwealth University · US

Funding

Regulation of Hepatic SphK2 by Bile Acids: Effects on Lipid MetabolismR01DK057543 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI HYLEMON, PHILLIP B, ZHOU, HUIPING ROSE · 2001 to 2015
$4.4M
Bile Acid and Sphingosine-1-phosphate Receptor-mediated Signaling in CholestasisR01DK104893 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI HYLEMON, PHILLIP B, ZHOU, HUIPING ROSE · 2016 to 2020
$2.0M
The role of Sphingosine Kinase 2 in alcoholic liver diseaseF30AA026470 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI KWONG, ERIC KWUN · 2017 to 2020
$170k
Impact of Alcohol on HIV Protease Inhibitor-induced ER Stress and LipotoxicityI01BX001390 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI ZHOU, HUIPING ROSE · 2012 to 2015
–
Mechanisms of Berberine for the Treatment of Non-Alcoholic Fatty Liver DiseaseI01BX004033 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI ZHOU, HUIPING ROSE · 2018 to 2021
–
BLR&D Research Career Scientist Award ApplicationIK6BX004477 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI HUIPING ZHOU · 2019 to 2026
–
BLRD VA I01 BX001390BLRD VA I01 BX004033BLRD VA IK6 BX004477NIAAA NIH HHS F30 AA026470NIDDK NIH HHS R01 DK057543NIDDK NIH HHS R01 DK104893
6 · The paper itself

Abstract

The liver is the central organ involved in lipid metabolism and the gastrointestinal (GI) tract is responsible for nutrient absorption and partitioning. Obesity, dyslipidemia and metabolic disorders are of increasing public health concern worldwide, and novel therapeutics that target both the liver and the GI tract (gut-liver axis) are much needed. In addition to aiding fat digestion, bile acids act as important signaling molecules that regulate lipid, glucose and energy metabolism via activating nuclear receptor, G protein-coupled receptors (GPCRs), Takeda G protein receptor 5 (TGR5) and sphingosine-1-phosphate receptor 2 (S1PR2). Sphingosine-1-phosphate (S1P) is synthesized by two sphingosine kinase isoforms and is a potent signaling molecule that plays a critical role in various diseases such as fatty liver, inflammatory bowel disease (IBD) and colorectal cancer. In this review, we will focus on recent findings related to the role of S1P-mediated signaling pathways in the gut-liver axis.

Indexed as

Gut-liver axisLiver diseases(S1PR2)Sphingosine-1-phosphate receptor 2Sphingosine-1-phosphate (S1P)Sphingosine kinase 2 (SphK2)

Identifiers

PMID31360579
PMCPMC6662730
OpenAlexW2919691687

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.