Evidence map›Paper›PMID 39005325›Full record

ArticlebioRxiv : the preprint server for biology2024

Epigenetic changes regulating the epithelial-mesenchymal transition in human trophoblast differentiation.

William E Ackerman, Mauricio M Rigo, Sonia C DaSilva-Arnold, Catherine Do, Mariam Tariq, Martha Salas, Angelica Castano, Stacy Zamudio, Benjamin Tycko, Nicholas P Illsley

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

William E AckermanDepartment of Obstetrics and Gynecology and AI.Health4All Center for Health Equity Using Machine Learning and Artificial Intelligence, University of Illinois College of Medicine, Chicago, USA.ORCID 0000-0001-7366-3903
Mauricio M RigoHackensack Meridian Health Center for Discovery and Innovation, Nutley, NJ.ORCID 0000-0002-1584-6194
Sonia C DaSilva-ArnoldDepartment of Obstetrics and Gynecology, Hackensack University Medical Center, Hackensack NJ.ORCID 0000-0003-2721-4626
Catherine DoHackensack Meridian Health Center for Discovery and Innovation, Nutley, NJ.ORCID 0000-0002-9796-4345
Mariam TariqHackensack Meridian Health Center for Discovery and Innovation, Nutley, NJ.
Martha SalasHackensack Meridian Health Center for Discovery and Innovation, Nutley, NJ.
Angelica CastanoHackensack Meridian Health Center for Discovery and Innovation, Nutley, NJ.
Stacy ZamudioDepartment of Obstetrics and Gynecology, Hackensack University Medical Center, Hackensack NJ.ORCID 0000-0002-5835-7251
Benjamin TyckoHackensack Meridian Health Center for Discovery and Innovation, Nutley, NJ.ORCID 0000-0001-7811-5164
Nicholas P IllsleyDepartment of Obstetrics and Gynecology, Hackensack University Medical Center, Hackensack NJ.ORCID 0000-0002-4336-2832

Funding

Genetic-epigenetic and aging interactions at COVID- 19 host response loci in Down syndrome and mouse modelsR01HD090180 · NICHD · HACKENSACK UNIVERSITY MEDICAL CENTER · PI TYCKO, BENJAMIN, YU, EUGENE · 2017 to 2021
$5.9M
Development of real-time, automated 3D ultrasound tools for the study of placental invasion and morphologyU01HD087209 · NICHD · HACKENSACK UNIVERSITY MEDICAL CENTER · PI COLLINS, SALLY LOUISE, ZAMUDIO, STACY · 2015 to 2015
$3.3M
NICHD NIH HHS R01 HD090180NICHD NIH HHS U01 HD087209
6 · The paper itself

Abstract

The phenotype of human placental extravillous trophoblast (EVT) at the end of pregnancy reflects both first trimester differentiation from villous cytotrophoblast (CTB) and later gestational changes, including loss of proliferative and invasive capacity. Invasion abnormalities are central to two major placental pathologies, preeclampsia and placenta accreta spectrum, so characterization of the corresponding normal processes is crucial. In this report, our gene expression analysis, using purified human CTB and EVT cells, highlights an epithelial-mesenchymal transition (EMT) mechanism underlying CTB-EVT differentiation and provides a trophoblast-specific EMT signature. In parallel, DNA methylation profiling shows that CTB cells, already hypomethylated relative to non-trophoblast cell lineages, show further genome-wide hypomethylation in the transition to EVT. However, a small subgroup of genes undergoes gains of methylation (GOM) in their regulatory regions or gene bodies, associated with differential mRNA expression (DE). Prominent in this GOM-DE group are genes involved in the EMT, including multiple canonical EMT markers and the EMT-linked transcription factor

Indexed as

differentiationepithelial-mesenchymal transitionmethylationTrophoblast

Identifiers

PMID39005325
PMCPMC11244995

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.