Evidence map›Paper›PMID 31518594›Full record

ReviewSteroids2019

Nox1 downregulators: A new class of therapeutics.

Matthias Barton, Matthias R Meyer, Eric R Prossnitz

Abstract readReview
In one paragraph

Review in Steroids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Oxidative Stress in Kidney Injury and Hypertension.Antioxidants (Basel, Switzerland) · 2024
    Review
  5. GPER expression prevents estrogen-induced urinary retention in obese mice.The Journal of steroid biochemistry and molecular biology · 2024
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. NOX Dependent ROS Generation and Cell Metabolism.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Attenuating glucose metabolism byAnnals of translational medicine · 2021
    Article
  16. Article
  17. GPER and Testicular Germ Cell Cancer.Frontiers in endocrinology · 2020
    Review
  18. 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.

Matthias BartonMolecular Internal Medicine, University of Zürich, Zürich, Switzerland; Andreas Grüntzig Foundation, Zürich, Switzerland. Electronic address: barton@access.uzh.ch.
Matthias R MeyerDivision of Cardiology, Triemli City Hospital, Zürich, Switzerland; Institute of Primary Care, University of Zürich, Zürich, Switzerland.
Eric R ProssnitzDivision of Molecular Medicine, Department of Internal Medicine, Health Sciences Center, Albuquerque, NM, USA; University of New Mexico Comprehensive Cancer Center, University of New Mexico, Health Sciences Center, Albuquerque, NM, USA.

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
Unfolded Protein Response and Autophagy in T Helper Cell Effector FunctionP20GM121176 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Monica Rosas Lemus · 2017 to 2026
$24.9M
Molecular Mechanisms and Applications of Novel ER/GPER-selective LigandsR01CA194496 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI ARTERBURN, JEFFREY B, PROSSNITZ, ERIC R · 2016 to 2025
$4.1M
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
NCI NIH HHS P30 CA118100NCI NIH HHS R01 CA163890NCI NIH HHS R01 CA194496NIGMS NIH HHS P20 GM121176
6 · The paper itself

Abstract

Chronic non-communicable diseases share the pathomechanism of increased reactive oxygen species (ROS) production by nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, known as Nox. The recent discovery that expression of Nox1, a Nox isoform that has been implicated in the pathogenesis of cardiovascular and kidney disease and cancer is regulated by the expression and activity of G protein-coupled estrogen receptor (GPER) led to the identification of orally active small-molecule GPER blockers as selective Nox1 downregulators (NDRs). Preclinical studies using NDRs have demonstrated beneficial effects in vascular disease, hypertension, and glomerular renal injury. These findings suggest the therapeutic potential of NDRs, which reduce Nox1 protein levels, not only for cardiovascular disease conditions including arterial hypertension, pulmonary hypertension, heart failure with preserved ejection fraction (HFpEF), and chronic renal disease, but also for other non-communicable diseases, such as cerebrovascular disease and vascular dementia, Alzheimer's disease, autoimmune diseases and cancer, in which elevated Nox1-derived ROS production plays a causal role.

Indexed as

Angiotensin II Type 1 Receptor BlockersAnimalsDrug DiscoveryHumansLigandsLosartanNADPH Oxidase 1Reactive Oxygen SpeciesAngiotensin II Type 1 Receptor BlockersLigandsLosartanNADPH Oxidase 1NOX1 protein, humanReactive Oxygen SpeciesChronic renal diseaseCoronary artery diseaseHeart failureHFpEFHypertensionNADPH oxidaseNon-communicable diseasesOxidative stressStrokeSuperoxideVascular

Identifiers

PMID31518594
PMCPMC6891104

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.