Evidence map›Paper›PMID 33605785›Full record

ArticleEnvironmental health perspectives2021

Bisphenol S and Epidermal Growth Factor Receptor Signaling in Human Placental Cytotrophoblasts.

Elvis Ticiani, Jeremy Gingrich, Yong Pu, Mathew Vettathu, Jacquelyn Davis, Denny Martin, Margaret G Petroff, Almudena Veiga-Lopez

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Current approaches and advances in placental toxicology.Trends in endocrinology and metabolism: TEM · 2026
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  3. Epidermal growth factor receptor in placental health and disease: pathways, dysfunction, and chemical disruption.Toxicological sciences : an official journal of the Society of Toxicology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Elvis TicianiDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
Jeremy GingrichDepartment of Pharmacology and Toxicology, Michigan State University (MSU), East Lansing, Michigan, USA.
Yong PuDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
Mathew VettathuSparrow Health System, Lansing, Michigan, USA.
Jacquelyn DavisSparrow Health System, Lansing, Michigan, USA.
Denny MartinSparrow Health System, Lansing, Michigan, USA.
Margaret G PetroffDepartment of Pathobiology and Diagnostic Investigation, MSU, East Lansing, Michigan, USA.
Almudena Veiga-LopezDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois, USA.
Sparrow Health System · USUniversity of Illinois Chicago · USMichigan State University · US

Funding

Pilot Program CoreP30ES027792 · NIEHS · UNIVERSITY OF CHICAGO · PI Gokhan M. Mutlu, Gail S Prins · 2017 to 2026
$13.6M
Reproductive and Developmental Sciences Training Program - T32T32HD087166 · NICHD · MICHIGAN STATE UNIVERSITY · PI Ronald L Chandler, Keith E Latham · 2016 to 2026
$2.5M
Placental adaptive mechanisms to environmental exposures.R01ES027863 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI VEIGA-LOPEZ, ALMUDENA · 2018 to 2022
$1.9M
Shared Placenta/Tumor Antigens and Maternal ImmunityR21HD083058 · NICHD · MICHIGAN STATE UNIVERSITY · PI PETROFF, MARGARET G · 2017 to 2018
$426k
NICHD NIH HHS R21 HD083058NICHD NIH HHS T32 HD087166NIEHS NIH HHS P30 ES027792NIEHS NIH HHS R01 ES027863
6 · The paper itself

Abstract

backgroundBisphenol S (BPS) is an endocrine-disrupting chemical and the second most abundant bisphenol detected in humans.

objectiveWe tested whether BPS interferes EGFR signaling and disrupts human cytotrophoblast syncytialization.

methodsWe first tested BPS competition for EGFR using an EGF/EGFR AlphaLISA assay. Using human primary term cytotrophoblast cells (hCTBs) and MDA-MD-231 cells, a breast cancer cell line with high EGFR expression, we evaluated EGFR downstream signaling and tested whether BPS could inhibit the EGF response by blocking EGFR activation. We also evaluated functional end points of EGFR signaling, including EGF endocytosis, cell proliferation, and syncytialization.

resultsBPS blocked EGF binding in a dose-dependent manner and reduced EGF-mediated phosphorylated EGFR in both cell types. We further confirmed that BPS acted as an EGFR antagonist as shown by a reduction in EGF internalization in both hCTBs and MDA-MD-231 cells. Finally, we demonstrated that BPS interfered with EGF-mediated cell processes, such as cell proliferation in MDA-MD-231 cells and syncytialization in hCTBs. EGF-mediated, but not spontaneous, hCTB syncytialization was fully blocked by BPS (

conclusionsGiven the role of EGFR in trophoblast proliferation and differentiation during placental development, this study suggests that exposures to BPS at environmentally relevant concentrations may result in placenta dysfunction, affecting fetal growth and development. https://doi.org/10.1289/EHP7297.

Indexed as

PlacentaTrophoblastsAnimalsBisphenol S CompoundsEpidermal Growth FactorErbB ReceptorsFemaleHumansPhenolsPregnancySheepSulfonesbisphenol SBisphenol S CompoundsEpidermal Growth FactorErbB ReceptorsPhenolsSulfones

Identifiers

PMID33605785
PMCPMC7894408
OpenAlexW3132433367

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.