Evidence map›Paper›PMID 33431410›Full record

ArticleBiology open2021

Bisphenol A promotes stress granule assembly and modulates the integrated stress response.

Marta M Fay, Daniella Columbo, Cecelia Cotter, Chandler Friend, Shawna Henry, Megan Hoppe, Paulina Karabelas, Corbyn Lamy, Miranda Lawell, Sarah Monteith and 8 more

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Connecting the Dots: Stress Granule and Cardiovascular Diseases.Journal of cardiovascular translational research · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. 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

18 authors at 3 institutions in 1 country.

Marta M FayDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, 02115 USA.
Daniella ColumboDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, 02115 USA.
Cecelia CotterDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Chandler FriendDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Shawna HenryDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Megan HoppeDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Paulina KarabelasDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Corbyn LamyDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Miranda LawellDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Sarah MonteithDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Christina NoyesDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Paige SalernoDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Jingyi WuDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Hedan Mindy ZhangDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA.
Paul J AndersonDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, 02115 USA.
Nancy KedershaDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, 02115 USA.
Pavel IvanovDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, 02115 USA pivanov@rics.bwh.harvard.edu nfarny@wpi.edu.ORCID 0000-0002-7986-7760
Natalie G FarnyDepartment of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA, 01609 USA pivanov@rics.bwh.harvard.edu nfarny@wpi.edu.ORCID 0000-0003-1143-4560
Worcester Polytechnic Institute · USBrigham and Women's Hospital · USBroad Institute · US

Funding

Cellular Stress Response MechanismsR35GM126901 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI ANDERSON, PAUL J. · 2018 to 2022
$2.9M
Biology of RNA G-quadruplexesR01GM126150 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI IVANOV, PAVEL · 2019 to 2023
$1.9M
tRNA-derived stress-induced RNAs and translational controlR01GM146997 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI IVANOV, PAVEL · 2022 to 2025
$1.6M
NIGMS NIH HHS R01 GM126150NIGMS NIH HHS R01 GM146997NIGMS NIH HHS R35 GM126901
6 · The paper itself

Abstract

Bisphenol-A (BPA) is a ubiquitous precursor of polycarbonate plastics that is found in the blood and serum of >92% of Americans. While BPA has been well documented to act as a weak estrogen receptor (ER) agonist, its effects on cellular stress are unclear. Here, we demonstrate that high-dose BPA causes stress granules (SGs) in human cells. A common estrogen derivative, β-estradiol, does not trigger SGs, indicating the mechanism of SG induction is not via the ER pathway. We also tested other structurally related environmental contaminants including the common BPA substitutes BPS and BPF, the industrial chemical 4-nonylphenol (4-NP) and structurally related compounds 4-EP and 4-VP, as well as the pesticide 2,4-dichlorophenoxyacetic acid (2,4-D). The variable results from these related compounds suggest that structural homology is not a reliable predictor of the capacity of a compound to cause SGs. Also, we demonstrate that BPA acts primarily through the PERK pathway to generate canonical SGs. Finally, we show that chronic exposure to a low physiologically relevant dose of BPA suppresses SG assembly upon subsequent acute stress. Interestingly, this SG inhibition does not affect phosphorylation of eIF2α or translation inhibition, thus uncoupling the physical assembly of SGs from translational control. Our work identifies additional effects of BPA beyond endocrine disruption that may have consequences for human health.

Indexed as

Stress, PhysiologicalAnimalsBenzhydryl CompoundsBisphenol A CompoundsCell LineeIF-2 KinaseEukaryotic Initiation Factor-2Gene Expression RegulationMicePhenolsStress GranulesBenzhydryl Compoundsbisphenol ABisphenol A CompoundseIF-2 KinaseEukaryotic Initiation Factor-2PhenolsBisphenol-AIntegrated stress responseStress granulesTranslational control

Identifiers

PMID33431410
PMCPMC7823164
OpenAlexW3120911408

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.