Evidence map›Paper›PMID 29186366›Full record

ArticleBiology of reproduction2018

Human endometrial stromal cell decidualization requires transcriptional reprogramming by PLZF.

Maria M Szwarc, Lan Hai, William E Gibbons, Mary C Peavey, Lisa D White, Qianxing Mo, David M Lonard, Ramakrishna Kommagani, Rainer B Lanz, Francesco J DeMayo and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  6. Progesterone inactivation in decidual stromal cells: A mechanism for inflammation-induced parturition.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  16. Review
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  19. Development and utilization of human decidualization reporter cell line uncovers new modulators of female fertility.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  20. Integrative analysis of the forkhead box A2 (FOXA2) cistrome for the human endometrium.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    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

11 authors at 3 institutions in 1 country.

Maria M SzwarcDepartment of Molecular & Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
Lan HaiDepartment of Molecular & Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
William E GibbonsDepartment of Obstetrics & Gynecology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
Mary C PeaveyDepartment of Obstetrics & Gynecology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
Lisa D WhiteGenomic & RNA Profiling Core Facility, Departments of Molecular & Human Genetics and Molecular & Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
Qianxing MoDepartment of Medicine and Dan L. Duncan Cancer Center, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
David M LonardDepartment of Molecular & Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
Ramakrishna KommaganiDepartment of Obstetrics & Gynecology, Washington University School of Medicine, St. Louis, Missouri, USA.
Rainer B LanzDepartment of Molecular & Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
Francesco J DeMayoReproductive and Developmental Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.
John P LydonDepartment of Molecular & Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, USA.
Baylor College of Medicine · USNational Institute of Environmental Health Sciences · USWashington University in St. Louis · US

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Molecular Analysis of Uterine ReceptivityR01HD042311 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI LYDON, JOHN P · 2009 to 2023
$4.8M
Small Molecule Src-2 Antagonists as Regulators of Sertoli Cell Function and MaleU01HD076596 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI LONARD, DAVID M · 2012 to 2016
$1.1M
GREB1 Action in Endometrial Function and DysfunctionR00HD080742 · NICHD · WASHINGTON UNIVERSITY · PI KOMMAGANI, RAMAKRISHNA · 2017 to 2019
$702k
NCI NIH HHS P30 CA125123NICHD NIH HHS R00 HD080742NICHD NIH HHS R01 HD042311NICHD NIH HHS U01 HD076596
6 · The paper itself

Abstract

Infertility and early embryo miscarriage is linked to inadequate endometrial decidualization. Although transcriptional reprogramming is known to drive decidualization in response to progesterone, the key signaling effectors that directly mediate this hormone response are not fully known. This knowledge gap is clinically significant because identifying the early signals that directly mediate progesterone-driven decidualization will address some of the current limitations in diagnosing and therapeutically treating patients at most risk for early pregnancy loss. We recently revealed that the promyelocytic leukemia zinc finger (PLZF) is a direct target of the progesterone receptor and is essential for decidualization of human endometrial stromal cells (hESCs). The purpose of this current work was to identify the genome-wide transcriptional program that is controlled by PLZF during hESC decidualization using an established in vitro hESC culture model, siRNA-mediated knockdown methods, and RNA-sequencing technology followed by bioinformatic analysis and validation. We discovered that PLZF is critical in the regulation of genes that are involved in cellular processes that are essential for the archetypal morphological and functional changes that occur when hESCs transform into epithelioid decidual cells such as proliferation and cell motility. We predict that the transcriptome datasets identified in this study will not only contribute to a broader understanding of PLZF-dependent endometrial decidualization at the molecular level but may advance the development of more effective molecular diagnostics and therapeutics for the clinical management of female infertility and subfertility that is based on a dysfunctional endometrium.

Indexed as

Cell MovementCell ProliferationCells, CulturedComputational BiologyDeciduaEndometriumFemaleGene Expression RegulationHumansPromyelocytic Leukemia Zinc Finger ProteinRNA InterferenceStromal CellsTranscriptomePromyelocytic Leukemia Zinc Finger Proteindeciduaendometriumfemale reproductive tractimplantationprogesterone/progesterone receptortranscriptional regulationuterus

Identifiers

PMID29186366
PMCPMC5819842
OpenAlexW2769221246

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.