Evidence map›Paper›PMID 27864940›Full record

ArticleBritish journal of pharmacology2017

Endogenous lysophosphatidic acid (LPA

Afrah Sattikar, Mark R Dowling, Elizabeth M Rosethorne

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Frontiers in pharmacology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Emerging structural biology of lipid G protein-coupled receptors.Protein science : a publication of the Protein Society · 2019
    Review
  11. Endogenous lysophosphatidic acid (LPABritish journal of pharmacology · 2017
    Article
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

3 authors at 3 institutions in 2 countries.

Afrah SattikarNovartis Institutes for Biomedical Research, Horsham, UK.
Mark R DowlingNovartis Institutes for Biomedical Research, Cambridge, MA, USA.
Elizabeth M RosethorneNovartis Institutes for Biomedical Research, Horsham, UK.ORCID 0000-0001-6877-2320
Novartis (United Kingdom) · GBNovartis (United States) · USUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeHuman lung fibroblasts (HLF) express high levels of the LPA EXPERIMENTAL APPROACH: Here, we have explored the signalling profiles of a range of LPA analogues in HLF that endogenously express the LPA KEY

resultsThese analyses demonstrated that the 16:0, 17:0, 18:2 and C18:1 LPA analogues appear to exhibit ligand bias between ERK phosphorylation and calcium mobilization when compared with 18:1 LPA, one of the most abundant forms of LPA that has been found in human plasma. CONCLUSION AND IMPLICATIONS: The importance of LPA as a key signalling molecule is shown by its widespread occurrence in biological fluids and its association with disease conditions such as fibrosis and cancer. These findings have important, as yet unexplored, implications for the (patho-) physiological signalling of the LPA

Indexed as

CalciumCells, CulturedFibroblastsFibrosisHumansLigandsLungLysophospholipidsMAP Kinase Signaling SystemNeoplasmsReceptors, Lysophosphatidic AcidSignal TransductionCalciumLigandslysophosphatidic acidLysophospholipidsReceptors, Lysophosphatidic Acid

Identifiers

PMID27864940
PMCPMC5241385
OpenAlexW2549838264

What Socratic 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 Socratic graph.