Evidence map›Paper›PMID 28444807›Full record

ReviewThe Journal of physiology2017

Raf kinase inhibitor protein: lessons of a better way for β-adrenergic receptor activation in the heart.

Kristina Lorenz, Marsha Rich Rosner, Theresa Brand, Joachim P Schmitt

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Raf Kinase Inhibitory Protein regulates the cAMP-dependent protein kinase signaling pathway through a positive feedback loop.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Conserved salt-bridge competition triggered by phosphorylation regulates the protein interactome.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. 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 at 3 institutions in 2 countries.

Kristina LorenzComprehensive Heart Failure Center, University of Würzburg, Versbacher Straße 9, 97078, Würzburg, Germany.ORCID 0000-0003-1137-668X
Marsha Rich RosnerBen May Department for Cancer Research, University of Chicago, Chicago, IL 60637, USA.
Theresa BrandLeibniz-Institut für Analytische Wissenschaften - ISAS - e.V., Bunsen-Kirchhoff-Straße 11, 44139, Dortmund, Germany.
Joachim P SchmittInstitute of Pharmacology and Clinical Pharmacology, Düsseldorf University Hospital, Universtitätsstraße 1, 40225, Düsseldorf, Germany.
University of Würzburg · DEDüsseldorf University Hospital · DEUniversity of Chicago · US

Funding

Regulation of RKIP FunctionR01GM121735 · NIGMS · UNIVERSITY OF CHICAGO · PI ROSNER, MARSHA R · 2017 to 2020
$1.6M
NIGMS NIH HHS R01 GM121735
6 · The paper itself

Abstract

Stimulation of β-adrenergic receptors (βARs) provides the most efficient physiological mechanism to enhance contraction and relaxation of the heart. Activation of βARs allows rapid enhancement of myocardial function in order to fuel the muscles for running and fighting in a fight-or-flight response. Likewise, βARs become activated during cardiovascular disease in an attempt to counteract the restrictions of cardiac output. However, long-term stimulation of βARs increases the likelihood of cardiac arrhythmias, adverse ventricular remodelling, decline of cardiac performance and premature death, thereby limiting the use of βAR agonists in the treatment of heart failure. Recently the endogenous Raf kinase inhibitor protein (RKIP) was found to activate βAR signalling of the heart without adverse effects. This review will summarize the current knowledge on RKIP-driven compared to receptor-mediated signalling in cardiomyocytes. Emphasis is given to the differential effects of RKIP on β

Indexed as

AnimalsCardiovascular DiseasesHeartHumansMyocardiumMyocytes, CardiacPhosphatidylethanolamine Binding ProteinReceptors, Adrenergic, betaSignal TransductionPhosphatidylethanolamine Binding ProteinReceptors, Adrenergic, betabeta-adrenergic receptorsheart failureRKIP

Identifiers

PMID28444807
PMCPMC5471367
OpenAlexW2883144558

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.