Evidence map›Paper›PMID 31408162›Full record

ArticleMolecular human reproduction2019

Interleukin-1β inhibits estrogen receptor-α, progesterone receptors A and B and biomarkers of human endometrial stromal cell differentiation: implications for endometriosis.

Jie Yu, Sarah L Berga, Wei Zou, Robert N Taylor

Open access · greenAbstract read
In one paragraph

Article in Molecular human reproduction, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

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  16. Uric acid participating in female reproductive disorders: a review.Reproductive biology and endocrinology : RB&E · 2021
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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

4 authors at 3 institutions in 2 countries.

Jie YuDepartment of Obstetrics and Gynecology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Sarah L BergaDepartment of Obstetrics and Gynecology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
Wei ZouHebei University of Science and Technology, Shijiazhuang, Hebei 050018, China.
Robert N TaylorDepartment of Obstetrics and Gynecology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.
University of Utah · USHebei University of Science and Technology · CNWake Forest University · US

Funding

1/2-Atlanta Center for Translational Research in Endometriosis (ACTRE)U01HD066439 · NICHD · EMORY UNIVERSITY · PI SIDELL, NEIL, THOMPSON, WINSTON E · 2010 to 2014
$1.4M
Neuroangiogenesis in Deep Infiltrating EndometriosisR21HD078818 · NICHD · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI TAYLOR, ROBERT N · 2015 to 2016
$424k
NICHD NIH HHS R21 HD078818NICHD NIH HHS U01 HD066439
6 · The paper itself

Abstract

Human blastocyst nidation in the uterus and successful pregnancy require coordinated endometrial expression of estrogen receptor (ER)-α, progesterone receptors (PR)-A and -B and the gap junction protein, connexin (Cx)43. Our prior work established that inflammation associated with conditions of reduced fecundity, particularly endometriosis, can perturb eutopic decidual function. In the current studies, we have modeled endometrial decidualization in primary human endometrial stromal cell cultures derived from normal controls (NESC) and from the eutopic endometria of women with endometriosis (EESC) to test the hypothesis that a proinflammatory cytokine, interleukin (IL)-1β, can disrupt stromal cell differentiation. The cells were grown under a standard protocol with hormones (10 nM 17β-estradiol, 100 nM progesterone and 0.5 mM dibutyryl cAMP) for up to 7 days in the absence or presence of IL-1β. Time-course experiments showed that IL-1β compromised decidual function in both NESC and EESC, which was accompanied by rapid phosphorylation of ER-α, PR and Cx43 and their cellular depletion. Inhibition of the extracellular signal-regulated kinase (ERK)1/2 pathway by a selective pharmacological blocker (PD98059) or siRNA interference, or the addition of hormones themselves, blocked the phosphorylation of ERK mediators; increased the production of steroid receptors, Cx43, prolactin, insulin-like growth factor binding protein-1 (IGFBP)-1 and vascular endothelial growth factor (VEGF) and accelerated the differentiation. The results indicate that inhibition of IL-1β can enhance decidualization in NESC and EESC in vitro. Strategies to interfere with this pathway might be implemented as an in vivo approach to enhance fertility in women with endometriosis and, potentially, other inflammatory pathologies.

Indexed as

Cell DifferentiationBiomarkersCase-Control StudiesCells, CulturedDown-RegulationEndometriosisEndometriumEstrogen Receptor alphaFemaleHumansInterleukin-1betaPeritoneal DiseasesReceptors, ProgesteroneStromal CellsBiomarkersESR1 protein, humanEstrogen Receptor alphaIL1B protein, humanInterleukin-1betaprogesterone receptor Aprogesterone receptor BReceptors, Progesteroneconnexin 43cytokinesdecidualizationendometriosisestrogen receptor-αinflammationinterleukin-1βprogesterone receptorssignal transductionuterus

Identifiers

PMID31408162
PMCPMC6821275
OpenAlexW2968943359

What OpenQuestion holds

Textmetadata
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.