Evidence map›Paper›PMID 26502914›Full record

ArticleEnvironmental health perspectives2016

Parabens and Human Epidermal Growth Factor Receptor Ligand Cross-Talk in Breast Cancer Cells.

Shawn Pan, Chaoshen Yuan, Abderrahmane Tagmount, Ruthann A Rudel, Janet M Ackerman, Paul Yaswen, Chris D Vulpe, Dale C Leitman

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2016. 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
2.3field-weighted citation impact, top 13% 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, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Minireview: Parabens Exposure and Breast Cancer.International journal of environmental research and public health · 2022
    Review
  7. Article
  8. The sex-specific association between maternal urinary paraben levels and offspring size at birth.Environmental science and pollution research international · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Environmental exposures, stem cells, and cancer.Pharmacology & therapeutics · 2019
    Review
  13. Traces of intact paraben molecules in endometrial carcinoma.Environmental science and pollution research international · 2019
    Article
  14. Article
  15. Homology models of mouse and rat estrogen receptor-Computational toxicology (Amsterdam, Netherlands) · 2019
    Article
  16. Review
  17. Review
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

8 authors at 3 institutions in 1 country.

Shawn PanDepartment of Nutritional Sciences and Toxicology, University of California, Berkeley, Berkeley, California, USA.
Chaoshen Yuan
Abderrahmane Tagmount
Ruthann A Rudel
Janet M Ackerman
Paul Yaswen
Chris D Vulpe
Dale C Leitman
University of California, Berkeley · USSilent Spring Institute · USLawrence Berkeley National Laboratory · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundXenoestrogens are synthetic compounds that mimic endogenous estrogens by binding to and activating estrogen receptors. Exposure to estrogens and to some xenoestrogens has been associated with cell proliferation and an increased risk of breast cancer. Despite evidence of estrogenicity, parabens are among the most widely used xenoestrogens in cosmetics and personal-care products and are generally considered safe. However, previous cell-based studies with parabens do not take into account the signaling cross-talk between estrogen receptor α (ERα) and the human epidermal growth factor receptor (HER) family.

objectivesWe investigated the hypothesis that the potency of parabens can be increased with HER ligands, such as heregulin (HRG).

methodsThe effects of HER ligands on paraben activation of c-Myc expression and cell proliferation were determined by real-time polymerase chain reaction, Western blots, flow cytometry, and chromatin immunoprecipitation assays in ERα- and HER2-positive human BT-474 breast cancer cells.

resultsButylparaben (BP) and HRG produced a synergistic increase in c-Myc mRNA and protein levels in BT-474 cells. Estrogen receptor antagonists blocked the synergistic increase in c-Myc protein levels. The combination of BP and HRG also stimulated proliferation of BT-474 cells compared with the effects of BP alone. HRG decreased the dose required for BP-mediated stimulation of c-Myc mRNA expression and cell proliferation. HRG caused the phosphorylation of serine 167 in ERα. BP and HRG produced a synergistic increase in ERα recruitment to the c-Myc gene.

conclusionOur results show that HER ligands enhanced the potency of BP to stimulate oncogene expression and breast cancer cell proliferation in vitro via ERα, suggesting that parabens might be active at exposure levels not previously considered toxicologically relevant from studies testing their effects in isolation. CITATION: Pan S, Yuan C, Tagmount A, Rudel RA, Ackerman JM, Yaswen P, Vulpe CD, Leitman DC. 2016. Parabens and human epidermal growth factor receptor ligand cross-talk in breast cancer cells. Environ Health Perspect 124:563-569; http://dx.doi.org/10.1289/ehp.1409200.

Indexed as

Cell Line, TumorErbB ReceptorsEstrogen Receptor alphaEstrogensGenes, mycHumansNeuregulin-1ParabensProto-Oncogene Proteins c-mycErbB ReceptorsESR1 protein, humanEstrogen Receptor alphaEstrogensNeuregulin-1ParabensProto-Oncogene Proteins c-myc

Identifiers

PMID26502914
PMCPMC4858398
OpenAlexW2180293274

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Registered trials

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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.