Evidence map›Paper›PMID 39253430›Full record

ArticlebioRxiv : the preprint server for biology2025

Aryl Hydrocarbon Receptor Activation Drives 2-Methoxy Estradiol Secretion in Human Trophoblast Stem Cell Development.

Vinay Shukla, Khursheed Iqbal, Hiroaki Okae, Takahiro Arima, Michael J Soares

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

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.

Vinay ShuklaInstitute for Reproductive and Developmental Sciences, University of Kansas Medical Center, Kansas City, KS 66160.ORCID 0000-0002-6181-269X
Khursheed IqbalInstitute for Reproductive and Developmental Sciences, University of Kansas Medical Center, Kansas City, KS 66160.ORCID 0000-0002-6742-4591
Hiroaki OkaeDepartment of Trophoblast Research, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto 860-0811 Japan.ORCID 0000-0002-1539-5063
Takahiro ArimaDepartment of Informative Genetics, Environment and Genome Research Center, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.
Michael J SoaresInstitute for Reproductive and Developmental Sciences, University of Kansas Medical Center, Kansas City, KS 66160.ORCID 0000-0001-7158-1592

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
TROPHOBLAST DIFFERENTIATIONR01HD020676 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI MICHAEL J SOARES · 1986 to 2026
$10.1M
Environmental Exposures, AHR Activation, and Placental Origins of DevelopmentR01ES029280 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI GRUNDBERG, ELIN, SOARES, MICHAEL J · 2018 to 2022
$2.6M
Trophoblast-Guided Uterine Transformation in the Establishment of PregnancyR01HD105734 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI MICHAEL J SOARES · 2022 to 2026
$2.2M
Endocrine Disruptors, Ahr Signaling, and PlacentationR21ES028957 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI IQBAL, KHURSHEED · 2018 to 2019
$421k
NICHD NIH HHS R01 HD020676NICHD NIH HHS R01 HD105734NIEHS NIH HHS R01 ES029280NIEHS NIH HHS R21 ES028957NIGMS NIH HHS P20 GM103418
6 · The paper itself

Abstract

study questionHow does activation of AHR signaling affect human trophoblast cell development and differentiation? SUMMARY ANSWER: AHR activation leads to altered gene expression but does not hinder the ability of trophoblast cells to remain in a stem cell state or differentiate into essential cell types, such as extravillous trophoblast cells (EVT) or syncytiotrophoblast (ST). It also promotes the production of 2 methoxy estradiol (2ME), a compound that could influence placental development. WHAT IS KNOWN ALREADY: The placenta serves both as a nutrient delivery system and a protective barrier against environmental toxins. AHR signaling is known to mediate cellular responses to environmental pollutants, potentially affecting trophoblast cell functions, but the specific impacts of AHR activation on these cells were not fully understood. STUDY DESIGN SIZE DURATION: This study utilized an in vitro model of human trophoblast stem (TS) cells to investigate the downstream effects of AHR activation. The study focused on both undifferentiated TS cells and cells undergoing differentiation. PARTICIPANTS/MATERIALS SETTING

methodsHuman trophoblast stem (TS) cells were used as the model system. Researchers examined the effects of TCDD exposure in both TS cells maintained in their stem state and those induced to differentiate into EVT or ST. The study assessed changes in gene expression, particularly focusing on MAIN RESULTS AND THE ROLE OF CHANCE: AHR activation stimulated the expression of LIMITATIONS REASONS FOR CAUTION: This study was conducted in vitro, which may not fully replicate human conditions. Further research is needed to confirm whether these findings apply to actual placental development in humans. WIDER IMPLICATIONS OF THE

findingsThe results suggest that AHR signaling activated by environmental pollutants could have a subtle but significant impact on placental development through mechanisms involving AHR activation. These findings may have broader implications for understanding how environmental factors affect fetal development. STUDY FUNDING/COMPETING INTERESTS: This work was funded by the National Institutes of Health: ES028957, HD020676, ES029280, HD105734 and the Sosland Foundation. The authors declare no conflicts of interest.

Indexed as

AHRPlacentaTCDDtrophoblast cells

Identifiers

PMID39253430
PMCPMC11383004

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.