Evidence map›Paper›PMID 37504219›Full record

ReviewBiomolecules & biomedicine2023

S1P/S1PR signaling pathway advancements in autoimmune diseases.

Jianbin Li, Yiping Huang, Yueqin Zhang, Pengcheng Liu, Mengxia Liu, Min Zhang, Rui Wu

Open access · diamondAbstract readReview
In one paragraph

Review in Biomolecules & biomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.5field-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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Sphingolipid Metabolism in the Pathogenesis of Hashimoto's Thyroiditis.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Opaganib Promotes Weight Loss and Suppresses High-Fat Diet-Induced Obesity and Glucose Intolerance.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Article
  13. Non-Malignant Granulocyte and Monocyte Disorders: An Update.British journal of biomedical science · 2025
    Review
  14. Review
  15. Article
  16. Review
  17. [Small Molecule Therapy for Inflammatory Bowel Disease: JAK Inhibitors and S1PR Modulators].The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2024
    Review
  18. Review
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Jianbin LiDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Yiping HuangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Yueqin ZhangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Pengcheng LiuDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Mengxia LiuDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Min ZhangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Rui WuDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingosine-1-phosphate (S1P) is a versatile sphingolipid that is generated through the phosphorylation of sphingosine by sphingosine kinase (SPHK). S1P exerts its functional effects by binding to the G protein-coupled S1P receptor (S1PR). This lipid mediator plays a pivotal role in various cellular activities. The S1P/S1PR signaling pathway is implicated in the pathogenesis of immune-mediated diseases, significantly contributing to the functioning of the immune system. It plays a crucial role in diverse physiological and pathophysiological processes, including cell survival, proliferation, migration, immune cell recruitment, synthesis of inflammatory mediators, and the formation of lymphatic and blood vessels. However, the full extent of the involvement of this signaling pathway in the development of autoimmune diseases remains to be fully elucidated. Therefore, this study aims to comprehensively review recent research on the S1P/S1PR axis in diseases related to autoimmunity.

Indexed as

Autoimmune DiseasesSignal TransductionHumansLysophospholipidsSphingolipidsSphingosineLysophospholipidsSphingolipidsSphingosinesphingosine 1-phosphate

Identifiers

PMID37504219
PMCPMC10655875
OpenAlexW4385302393

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.