Evidence map›Paper›PMID 34944751›Full record

ArticleBiomedicines2021

Epigenetic Dysregulation of Trophoblastic Gene Expression in Gestational Trophoblastic Disease.

Zoltan Szabolcsi, Amanda Demeter, Peter Kiraly, Andrea Balogh, Melissa L Wilson, Jennifer R King, Szabolcs Hetey, Zsolt Gelencser, Koji Matsuo, Beata Hargitai and 7 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
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

17 authors at 4 institutions in 3 countries.

Zoltan SzabolcsiSystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.ORCID 0000-0003-0937-9857
Amanda DemeterSystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.
Peter KiralySystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.
Andrea BaloghSystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.
Melissa L WilsonDepartment of Population and Public Health Sciences, University of Southern California, Los Angeles, CA 90033, USA.
Jennifer R KingDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Szabolcs HeteySystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.ORCID 0000-0002-5948-8501
Zsolt GelencserSystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.
Koji MatsuoDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Beata HargitaiBirmingham Women's NHS Foundation Trust, University of Birmingham, Birmingham B15 2TG, UK.
Paulette Mhawech-FaucegliaDepartment of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Petronella HupucziMaternity Private Clinic, H-1126 Budapest, Hungary.
Andras SzilagyiSystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.ORCID 0000-0002-1773-6861
Zoltan PappMaternity Private Clinic, H-1126 Budapest, Hungary.
Lynda D RomanDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Victoria K CortessisDepartment of Population and Public Health Sciences, University of Southern California, Los Angeles, CA 90033, USA.
Nandor Gabor ThanSystems Biology of Reproduction Research Group, Research Centre for Natural Sciences, Institute of Enzymology, H-1117 Budapest, Hungary.
Institute of Molecular Life Sciences · HUUniversity of Southern California · USSemmelweis University · HUBirmingham Women’s and Children’s NHS Foundation Trust · GB

Funding

Hungarian Academy of Sciences Momentum Grant No LP2014-7/2014Hungarian Academy of Sciences Premium Postdoc_2019-436 Grant and Young Researcher FellowshipsHungarian Ministry for National Economy Grant No VEKOP-2.3.3-15-2017-0014MedInProt Protein Science Research Synergy IV and Adhoc Program GrantsMinistry for Innovation and Technology FIEK_16-1-2016-0005Ministry for Innovation and Technology National Research, Development and Innovation Fund OTKA K124862Ministry for Innovation and Technology National Research, Development and Innovation Fund OTKA K128262University of Southern California Gynecologic Oncology Research Fund
6 · The paper itself

Abstract

Gestational trophoblastic diseases (GTDs) have not been investigated for their epigenetic marks and consequent transcriptomic changes. Here, we analyzed genome-wide DNA methylation and transcriptome data to reveal the epigenetic basis of disease pathways that may lead to benign or malignant GTDs. RNA-Seq, mRNA microarray, and Human Methylation 450 BeadChip data from complete moles and choriocarcinoma cells were bioinformatically analyzed. Paraffin-embedded tissues from complete moles and control placentas were used for tissue microarray construction, DNMT3B immunostaining and immunoscoring. We found that DNA methylation increases with disease severity in GTDs. Differentially expressed genes are mainly upregulated in moles while predominantly downregulated in choriocarcinoma. DNA methylation principally influences the gene expression of villous trophoblast differentiation-related or predominantly placenta-expressed genes in moles and choriocarcinoma cells. Affected genes in these subsets shared focal adhesion and actin cytoskeleton pathways in moles and choriocarcinoma. In moles, cell cycle and differentiation regulatory pathways, essential for trophoblast/placental development, were enriched. In choriocarcinoma cells, hormone biosynthetic, extracellular matrix-related, hypoxic gene regulatory, and differentiation-related signaling pathways were enriched. In moles, we found slight upregulation of DNMT3B protein, a developmentally important de novo DNA methylase, which is strongly overexpressed in choriocarcinoma cells that may partly be responsible for the large DNA methylation differences. Our findings provide new insights into the shared and disparate molecular pathways of disease in GTDs and may help in designing new diagnostic and therapeutic tools.

Indexed as

choriocarcinomagestational trophoblastic diseasehydatidiform moleplacental-specific genesystems biologytrophoblast differentiation

Identifiers

PMID34944751
PMCPMC8698431
OpenAlexW4200427412

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.