Evidence map›Paper›PMID 18322542›Full record

ReviewKidney international2008

Sphingosine-1-phosphate receptors: biology and therapeutic potential in kidney disease.

S-K Jo, A Bajwa, A S Awad, K R Lynch, M D Okusa

Open access · greenAbstract readReview
In one paragraph

Review in Kidney international, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

47 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Sphingolipid signaling in kidney diseases.American journal of physiology. Renal physiology · 2025
    Review
  3. Article
  4. Article
  5. Role of G protein coupled receptors in acute kidney injury.Cell communication and signaling : CCS · 2024
    Review
  6. Article
  7. Article
  8. Emerging roles for lymphatics in acute kidney injury: Beneficial or maleficent?Experimental biology and medicine (Maywood, N.J.) · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Sphingosine-1-phosphate signaling in blood pressure regulation.American journal of physiology. Renal physiology · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Sphingosine Kinase 2 Deficiency Attenuates Kidney FibrosisJournal of the American Society of Nephrology : JASN · 2017
    Article
  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

5 authors at 1 institution in 2 countries.

S-K JoDepartment of Medicine, University of Virginia, Charlottesville, Virginia 22908, USA.
A Bajwa
A S Awad
K R Lynch
M D Okusa
University of Virginia · US

Funding

Leukocyte Trafficking in Acute Renal FailureR01DK062324 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI OKUSA, MARK DOUGLAS · 2003 to 2016
$4.4M
Molecular Pharmacology of Sphingosine 1-PhosphateR01GM067958 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LYNCH, KEVIN R. · 2004 to 2014
$3.7M
Kidney Disease and InflammationT32DK072922 · NIDDK · UNIVERSITY OF VIRGINIA · PI OKUSA, MARK DOUGLAS · 2006 to 2020
$2.6M
ADENOSINE AND RENAL INJURYR01DK056223 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI OKUSA, MARK DOUGLAS · 2000 to 2009
$1.9M
Lysophosphatidic Acid Receptors and Acute Renal FailureR01DK065957 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI OKUSA, MARK DOUGLAS · 2004 to 2007
$1.3M
Podocyte Microenvironment in Diabetic NephropathyR00DK077444 · NIDDK · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI AWAD, ALAA S · 2009 to 2011
$747k
Podocyte Microenvironment in Diabetic NephropathyK99DK077444 · NIDDK · UNIVERSITY OF VIRGINIA · PI AWAD, ALAA S · 2007 to 2008
$181k
NIDDK NIH HHS K99 DK077444NIDDK NIH HHS R00 DK077444NIDDK NIH HHS R01 DK056223NIDDK NIH HHS R01 DK062324NIDDK NIH HHS R01 DK065957NIDDK NIH HHS R01 DK56223NIDDK NIH HHS R01 DK62324NIDDK NIH HHS T32 DK072922NIGMS NIH HHS R01 GM067958NIGMS NIH HHS R01GM067958
6 · The paper itself

Abstract

The major sphingolipid metabolite, sphingosine-1-phosphate (S1P), has important biological functions. S1P is the ligand for a family of five G-protein-coupled receptors with distinct signaling pathways that regulate angiogenesis, vascular maturation, immunity, chemotaxis, and other important biological pathways. Recently, clinical trials have targeted S1P receptors (S1PRs) for autoimmune diseases and transplantation and have generated considerable interest in developing additional, more selective compounds. This review summarizes current knowledge on the biology of S1P and S1PRs that forms the basis for future drug development and the treatment of kidney disease.

Indexed as

Drug DesignAnimalsCell SurvivalHumansKidney DiseasesLysophospholipidsMiceReceptors, LysosphingolipidSphingosineLysophospholipidsReceptors, LysosphingolipidSphingosinesphingosine 1-phosphate

Identifiers

PMID18322542
PMCPMC2614447
OpenAlexW1970447847

What OpenQuestion holds

Textmetadata
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.