Evidence map›Paper›PMID 27803283›Full record

ArticleScience signaling2016

Obligatory role for GPER in cardiovascular aging and disease.

Matthias R Meyer, Natalie C Fredette, Christoph Daniel, Geetanjali Sharma, Kerstin Amann, Jeffrey B Arterburn, Matthias Barton, Eric R Prossnitz

Abstract read
In one paragraph

Article in Science signaling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  7. GPER expression prevents estrogen-induced urinary retention in obese mice.The Journal of steroid biochemistry and molecular biology · 2024
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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

8 authors at 3 institutions in 2 countries.

Matthias R Meyer *University of New Mexico Health Sciences Center, Department of Internal Medicine, Albuquerque, NM 87131, USA.
Natalie C Fredette *University of New Mexico Health Sciences Center, Department of Internal Medicine, Albuquerque, NM 87131, USA.
Christoph DanielFriedrich-Alexander-University of Erlangen-Nürnberg, Department of Nephropathology, 91054 Erlangen, Germany.
Geetanjali SharmaUniversity of New Mexico Health Sciences Center, Department of Internal Medicine, Albuquerque, NM 87131, USA.
Kerstin AmannFriedrich-Alexander-University of Erlangen-Nürnberg, Department of Nephropathology, 91054 Erlangen, Germany.
Jeffrey B ArterburnNew Mexico State University, Department of Chemistry and Biochemistry, Las Cruces, NM 88003, USA.
Matthias BartonUniversity of Zürich, Molecular Internal Medicine, 8057 Zürich, Switzerland.
Eric R ProssnitzUniversity of New Mexico Health Sciences Center, Department of Internal Medicine, Albuquerque, NM 87131, USA.
University of New Mexico · USNew Mexico State University · USUniversity of Zurich · CH

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
UNM HSC Clinical and Translational Science CenterUL1TR001449 · NCATS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CAMPEN, MATTHEW J, PANDHI, NANCY · 2015 to 2024
$36.9M
MINORITY INSTITUTIONAL RESEARCH TRAINING PROGRAM (T32)T32HL007736 · NHLBI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI RESTA, THOMAS C · 1993 to 2025
$6.5M
Integrative Program in CNS Pathophysiology ResearchP30GM103400 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LIU, KE JIAN · 2012 to 2016
$4.7M
G protein-coupled estrogen receptor GPER and breast carcinogenesisR01CA163890 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI PROSSNITZ, ERIC R · 2012 to 2023
$3.3M
Development of GPR30-Selective LigandsR01CA127731 · NCI · UNIVERSITY OF NEW MEXICO · PI ARTERBURN, JEFFREY B, OPREA, TUDOR I · 2008 to 2012
$1.7M
NCATS NIH HHS UL1 TR001449NCI NIH HHS P30 CA118100NCI NIH HHS R01 CA127731NCI NIH HHS R01 CA163890NHLBI NIH HHS T32 HL007736NIGMS NIH HHS P30 GM103400
6 · The paper itself

Abstract

Pharmacological activation of the heptahelical G protein-coupled estrogen receptor (GPER) by selective ligands counteracts multiple aspects of cardiovascular disease. We thus expected that genetic deletion or pharmacological inhibition of GPER would further aggravate such disease states, particularly with age. To the contrary, we found that genetic ablation of Gper in mice prevented cardiovascular pathologies associated with aging by reducing superoxide (⋅O

Indexed as

AgingAnimalsBenzodioxolesHeart FailureHypertensionMiceMice, KnockoutNADPH Oxidase 1QuinolinesReceptors, EstrogenSuperoxidesBenzodioxolesG36 compoundNADPH Oxidase 1NOX1 protein, mouseQuinolinesReceptors, EstrogenSuperoxides

Identifiers

PMID27803283
PMCPMC5124501
OpenAlexW2547446918

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.