Evidence map›Paper›PMID 33923905›Full record

ReviewInternational journal of molecular sciences2021

Estrogen Receptor Functions and Pathways at the Vascular Immune Interface.

Aida Dama, Chiara Baggio, Carlotta Boscaro, Mattia Albiero, Andrea Cignarella

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Aida DamaDepartment of Medicine, University of Padova, 35128 Padova, Italy.
Chiara BaggioDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35128 Padova, Italy.
Carlotta BoscaroDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35128 Padova, Italy.
Mattia AlbieroDepartment of Medicine, University of Padova, 35128 Padova, Italy.
Andrea CignarellaDepartment of Medicine, University of Padova, 35128 Padova, Italy.ORCID 0000-0002-4820-4876
University of Padua · IT

Funding

Università degli Studi di Padova MSCA Seal of Excellence@UNIPD 2019
6 · The paper itself

Abstract

Estrogen receptor (ER) activity mediates multiple physiological processes in the cardiovascular system. ERα and ERβ are ligand-activated transcription factors of the nuclear hormone receptor superfamily, while the G protein-coupled estrogen receptor (GPER) mediates estrogenic signals by modulating non-nuclear second messengers, including activation of the MAP kinase signaling cascade. Membrane localizations of ERs are generally associated with rapid, non-genomic effects while nuclear localizations are associated with nuclear activities/transcriptional modulation of target genes. Gender dependence of endothelial biology, either through the action of sex hormones or sex chromosome-related factors, is becoming increasingly evident. Accordingly, cardiometabolic risk increases as women transition to menopause. Estrogen pathways control angiogenesis progression through complex mechanisms. The classic ERs have been acknowledged to function in mediating estrogen effects on glucose metabolism, but 17β-estradiol also rapidly promotes endothelial glycolysis by increasing glucose transporter 1 (GLUT1) and 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3) levels through GPER-dependent mechanisms. Estrogens alter monocyte and macrophage phenotype(s), and induce effects on other estrogen-responsive cell lineages (e.g., secretion of cytokines/chemokines/growth factors) that impact macrophage function. The pharmacological modulation of ERs for therapeutic purposes, however, is particularly challenging due to the lack of ER subtype selectivity of currently used agents. Identifying the determinants of biological responses to estrogenic agents at the vascular immune interface and developing targeted pharmacological interventions may result in novel improved therapeutic solutions.

Indexed as

AnimalsEstrogensGlucose Transporter Type 1HumansMacrophagesMonocytesPhosphofructokinase-2Receptors, EstrogenReceptors, G-Protein-CoupledSignal TransductionEstrogensGlucose Transporter Type 1Phosphofructokinase-2Receptors, EstrogenReceptors, G-Protein-Coupledendotheliumestrogen receptorsestrogensgender differencesmacrophagesmonocytes

Identifiers

PMID33923905
PMCPMC8073008
OpenAlexW3155357496

What OpenQuestion 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 OpenQuestion graph.