Evidence map›Paper›PMID 29450131›Full record

ReviewBiochimie open2016

Dimethyl-Benz(a)anthracene: A mammary carcinogen and a neuroendocrine disruptor.

Bernard Kerdelhué, Claude Forest, Xavier Coumoul

Open access · hybridAbstract readReview
In one paragraph

Review in Biochimie open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Rat Models of Breast Cancer.Advances in experimental medicine and biology · 2025
    Review
  5. Article
  6. Effect ofVeterinary world · 2024
    Article
  7. Exposure to brominated flame retardantsFrontiers in endocrinology · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Antitumour Property ofBreast cancer : basic and clinical research · 2020
    Article
  17. Review
  18. 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

3 authors at 2 institutions in 1 country.

Bernard KerdelhuéCNRS UMR 8601, Chimie et Biochimie Pharmacologiques et Toxicologiques, Université Paris Descartes, Faculté des Sciences Fondamentales et Biomédicales, 45 rue des Saints Pères, 75006 Paris, France.
Claude ForestINSERM UMR-S 1124, Université Paris Descartes, PRES Sorbonne Paris Cité, Pharmacologie Toxicologie et Signalisation Cellulaire, Faculté des Sciences Fondamentales et Biomédicales, 45 rue des Saints Pères, 75006 Paris, France.
Xavier CoumoulINSERM UMR-S 1124, Université Paris Descartes, PRES Sorbonne Paris Cité, Pharmacologie Toxicologie et Signalisation Cellulaire, Faculté des Sciences Fondamentales et Biomédicales, 45 rue des Saints Pères, 75006 Paris, France.
Sorbonne Paris Cité · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polycyclic Aromatic Hydrocarbons (PAHs) are potent carcinogens. Among these, dimethylbenz(a)anthracene (DMBA) is well known for its capacity to induce mammary carcinomas in female Sprague-Dawley (SD) rats. Ovariectomy suppresses the susceptibility of this model to DMBA, thus suggesting that the inducible action of the carcinogen depends on ovarian hormones. The promotion of DMBA-induced adenocarcinoma is accompanied by a series of neuroendocrine disruptions of both Hypothalamo-Pituitary-Gonadal (HPG) and Hypothalamo-Pituitary-Adrenal (HPA) axes and of the secretion of melatonin during the latency period of 2 months that precedes the occurrence of the first mammary tumor. The present review analyses the various neuroendocrine disruptions that occur along the HPG and the HPA axes, and the marked inhibitory effect of the carcinogen on melatonin secretion. The possible relationships between the neuroendocrine disruptions, which essentially consist in an increased pre-ovulatory secretion of 17β-estradiol and prolactin, associated with a marked reduction of melatonin secretion, and the decrease in gene expression of the receptors for aryl-hydrocarbons receptor (AhR) and 17β-estradiol (ERα; ERβ) are also discussed.

Indexed as

ACTH, Adrenocorticotropic hormoneAhR, Aryl hydrocarbon ReceptorARNT, AhR nuclear translocatorCRH, Corticotropin releasing hormoneCYP, Cytochromes P450Dimethylbenz(a)anthraceneDMBA, Dimethylbenz(a)anthraceneE2, 17β-estradiolERα and ERβ, Estrogen receptorFemale ratFSH, Folliculo-Stimulating HormoneGnRH, Gonadotropin-Releasing HormoneHPA, Hypothalamo-Pituitary-AdrenalHPG, Hypothalamo-Pituitary-GonadalLH, Luteinizing hormoneMammary cancerNeuroendocrine disruptionPAHs, Polycyclic Aromatic HydrocarbonsPRL, ProlactinSD, Sprague-DawleyTCDD, 2,3,7,8-tetrachlorodibenzo-p-dioxinXRE, Xenobiotic response elements

Identifiers

PMID29450131
PMCPMC5801823
OpenAlexW2530617275

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.