Evidence map›Paper›PMID 21707517›Full record

ReviewCurrent molecular medicine2011

Prostacyclin receptor regulation--from transcription to trafficking.

C Midgett, J Stitham, K A Martin, J Hwa

Abstract readReview
In one paragraph

Review in Current molecular medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. 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

4 authors.

C MidgettDepartment of Internal Medicine, Section of Cardiovascular Medicine, Yale School of Medicine, Cardiovascular Research Center, 300 George Street, Rm 759H, New Haven, CT 06511, USA.
J Stitham
K A Martin
J Hwa

Funding

Pharmacogenetics of the human prostacyclin receptor.R01HL074190 · NHLBI · YALE UNIVERSITY · PI HWA, JOHN · 2004 to 2013
$3.3M
NHLBI NIH HHS R01 HL074190
6 · The paper itself

Abstract

The prostacyclin receptor (IP--International Union of Pharmacology nomenclature) is a member of the seven transmembrane G-protein coupled receptor (GPCR) superfamily. Recent concerns with selective and non-selective COX-1/COX-2 inhibition have exposed an important cardioprotective role for IP in preventing atherothrombosis. Receptor dysfunction (genetic variants) or reduced signaling (COX-2 inhibition) in high cardiovascular risk patients leads to increased cardiovascular events. These clinical observations have also been confirmed genetically by mouse knockout studies. Thus, receptor regulation is paramount in ensuring correct function in the prevention of atherothrombosis. This review summarizes recent literature on how this important receptor is regulated, from transcription to transport (to and from the membrane surface). These regulatory processes are critical in ensuring that IP receptors are adequately expressed and functional on the cell surface.

Indexed as

Transcription, GeneticAnimalsCell MembraneCyclooxygenase 2HumansProtein MultimerizationProtein TransportReceptors, EpoprostenolCyclooxygenase 2Receptors, Epoprostenol

Identifiers

PMID21707517
PMCPMC3647249

What OpenQuestion holds

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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.