Evidence map›Paper›PMID 31681507›Full record

ArticleBioResearch open access2019

Hormone-Like Effects of Bisphenol A on p53 and Estrogen Receptor Alpha in Breast Cancer Cells.

Victoria Lloyd, Mia Morse, Betsy Purakal, Jordan Parker, Paige Benard, Michael Crone, Samantha Pfiffner, Monica Szmyd, Sumi Dinda

Open access · diamondAbstract read
In one paragraph

Article in BioResearch open access, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Victoria LloydDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Mia MorseDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Betsy PurakalDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Jordan ParkerDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Paige BenardDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Michael CroneDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Samantha PfiffnerDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Monica SzmydDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Sumi DindaDepartment of Biomedical Diagnostic and Therapeutic Sciences, School of Health Sciences, Center of Biomedical Research, Oakland University, Rochester, Michigan.
Oakland University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bisphenol A (BPA) is a polymerizing agent commonly found in plastics that has been linked to xenoestrogenic activity. In this study, we analyzed the estrogen-like effects of BPA on the expression of estrogen receptor (ER)α and p53 with hormonal and antihormonal treatments in T-47D and MCF-7 cells. Cells were cultured in medium containing 5% charcoal-stripped fetal bovine serum for 6 days to deplete any endogenous steroids or effectors. The cells were then treated for 24 h with 600 nM BPA, which was determined to be the optimal value by a concentration study of BPA from 1 nM to 2 μM. Extracted cellular proteins were quantified and subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)/Western blot analysis. The cell proliferation assays were quantified upon exposure to BPA. Laser confocal microscopy was performed to determine the cytolocalization of p53 and ERα upon treatment with BPA. Western blot analysis revealed that BPA caused an increase in the cellular protein p53 in a concentration-dependent manner. While treatment with BPA did not affect the cytolocalization of p53, an increase in cell proliferation was observed. Our studies provide interesting leads to delineate the possible mechanistic relationship among BPA, ER, and tumor suppressor proteins in breast cancer cells.

Indexed as

antiestrogensBPAbreast cancerERαestrogenp53tumor suppressors

Identifiers

PMID31681507
PMCPMC6823605
OpenAlexW2986452896

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.