Evidence map›Paper›PMID 23962825›Full record

ReviewTrends in cardiovascular medicine2014

Functional role, mechanisms of regulation, and therapeutic potential of regulator of G protein signaling 2 in the heart.

Peng Zhang, Ulrike Mende

Open access · greenAbstract readReview
In one paragraph

Review in Trends in cardiovascular medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Transcriptomic signatures for ovulation in vertebrates.General and comparative endocrinology · 2017
    Article
  11. Review
  12. Gq signaling causes glomerular injury by activating TRPC6.The Journal of clinical investigation · 2015
    Article
  13. Regulator of G Protein Signaling 2: A Versatile Regulator of Vascular Function.Progress in molecular biology and translational science · 2015
    Review
  14. Roles of cGMP-dependent protein kinase I (cGKI) and PDE5 in the regulation of Ang II-induced cardiac hypertrophy and fibrosis.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  15. 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

2 authors at 2 institutions in 1 country.

Peng ZhangCardiovascular Research Center, Cardiology Division, Rhode Island Hospital and Alpert Medical School of Brown University, Providence, RI, USA.
Ulrike MendeCardiovascular Research Center, Cardiology Division, Rhode Island Hospital and Alpert Medical School of Brown University, Providence, RI, USA. Electronic address: ulrike_mende@brown.edu.
Brown University · USRhode Island Hospital · US

Funding

Uncoupling of IL-1 beta and VEGF-A Crosstalk Contributes to Impaired Arteriogenesis Response to Ischemia in Chronic Diabetes MellitusP20GM103652 · NIGMS · OCEAN STATE RESEARCH INSTITUTE, INC. · PI ROUNDS, SHARON IRENE SMITH · 2013 to 2022
$21.3M
COBRE for Perinatal BiologyP20GM103537 · NIGMS · WOMEN AND INFANTS HOSPITAL-RHODE ISLAND · PI PADBURY, JAMES F · 2012 to 2012
$2.1M
Regulation of Gq Signaling in Cardiac Fibroblasts and its Role in Cardiac RemodelR01HL114784 · NHLBI · RHODE ISLAND HOSPITAL · PI MENDE, ULRIKE · 2013 to 2016
$2.0M
RGS Regulation of Cardiac Signaling and HypertrophyR01HL080127 · NHLBI · RHODE ISLAND HOSPITAL · PI MENDE, ULRIKE · 2006 to 2010
$1.8M
Advancing Experimental Models to Study Intercellular Crosstalk of Cardiac CellsR21HL113918 · NHLBI · RHODE ISLAND HOSPITAL · PI MENDE, ULRIKE · 2013 to 2014
$428k
NHLBI NIH HHS HL113918NHLBI NIH HHS HL80127NHLBI NIH HHS R01 HL080127NHLBI NIH HHS R01 HL114784NHLBI NIH HHS R21 HL113918NIGMS NIH HHS 5P20RR018728-10/8P20GM103537-10NIGMS NIH HHS P20 GM103537NIGMS NIH HHS P20 GM103652
6 · The paper itself

Abstract

G protein-mediated signal transduction is essential for the regulation of cardiovascular function, including heart rate, growth, contraction, and vascular tone. Regulators of G protein Signaling (RGS proteins) fine-tune G protein-coupled receptor-induced signaling by regulating its magnitude and duration through direct interaction with the α subunits of heterotrimeric G proteins. Changes in the RGS protein expression and/or function in the heart often lead to pathophysiological changes and are associated with cardiac disease in animals and humans, including hypertrophy, fibrosis development, heart failure, and arrhythmias. This article focuses on Regulator of G protein Signaling 2 (RGS2), which is widely expressed in many tissues and is highly regulated in its expression and function. Most information to date has been obtained in biochemical, cellular, and animal studies, but data from humans is emerging. We review recent advances on the functional role of cardiovascular RGS2 and the mechanisms that determine its signaling selectivity, expression, and functionality. We highlight key unanswered questions and discuss the potential of RGS2 as a therapeutic target.

Indexed as

Signal TransductionAnimalsCardiovascular DiseasesHumansMolecular Targeted TherapyMyocardiumRGS ProteinsRGS2 protein, humanRGS Proteins

Identifiers

PMID23962825
PMCPMC3948174
OpenAlexW1990833817

What OpenQuestion holds

Textmetadata
LicenceTDM
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.