Evidence map›Paper›PMID 26852889›Full record

ArticleInternational journal of experimental pathology2016

Prenatal exposure to ethinylestradiol alters the morphologic patterns and increases the predisposition for prostatic lesions in male and female gerbils during ageing.

Ana P S Perez, Manoel F Biancardi, Cássia R S Caires, Luiz R Falleiros-Junior, Rejane M Góes, Patricia S L Vilamaior, Fernanda C A Santos, Sebastião R Taboga

Open access · greenAbstract read
In one paragraph

Article in International journal of experimental pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. DNA methylation in development and disease: an overview for prostate researchers.American journal of clinical and experimental urology · 2018
    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.

Ana P S PerezDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas -UNICAMP, Campinas, São Paulo, Brazil.
Manoel F BiancardiDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas -UNICAMP, Campinas, São Paulo, Brazil.
Cássia R S CairesDepartment of Biology, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University - IBILCE/UNESP, São José do Rio Preto, São Paulo, Brazil.
Luiz R Falleiros-JuniorDepartment of Biology, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University - IBILCE/UNESP, São José do Rio Preto, São Paulo, Brazil.
Rejane M GóesDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas -UNICAMP, Campinas, São Paulo, Brazil.
Patricia S L VilamaiorDepartment of Biology, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University - IBILCE/UNESP, São José do Rio Preto, São Paulo, Brazil.
Fernanda C A SantosDepartment of Morphology, Federal University of Goiás - UFG, Goiânia, Goiás, Brazil.
Sebastião R TabogaDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas -UNICAMP, Campinas, São Paulo, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal de Goiás · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ethinylestradiol (EE) is an endocrine disruptor (ED) which acts as an oestrogen agonist; this compound is known as an oral contraceptive. Male and female rodents exposed to EE during critical time points of development, such as in the prenatal period, show alterations in their reproductive tract during adulthood. Few studies have placed an emphasis on the effects of EE during ageing. Thus, this study had as it's objective the analysis of the morphological and immunohistochemical effects of exposure to EE in the prenatal period on ventral male prostate and female prostate of gerbils (Meriones unguiculatus) during ageing. The animals were exposed to EE (15 μg/kg/day) during the 18-22th days of prenatal life (EE/PRE group), and the analyses were performed when the male and female reached 12 months of age. Our results showed an increase in the development of prostatic intraepithelial neoplasia (PIN), which was observed in the male and female prostate of EE/PRE groups. Immunohistochemistry showed a rise in prostatic epithelial and basal cells immunoreactivity, respectively, and to AR and p63 in the male EE/PRE. There were alterations in the morphological pattern of the prostatic glands and increase in predisposition to emergence of prostatic lesions of both sexes during ageing. Despite male and female having been exposed to the same doses of EE, the "exposure to EE promoted modifications" more accentuated in the male prostate. Thus the male gland is more sensitive to the action of this synthetic oestrogen than the female prostate.

Indexed as

AgingAnimalsAnimals, NewbornDisease SusceptibilityEstradiolEthinyl EstradiolFemaleGerbillinaeMalePregnancyPrenatal Exposure Delayed EffectsProstateProstatic Intraepithelial NeoplasiaProstatic NeoplasmsReceptors, AndrogenTestosteroneEstradiolEthinyl EstradiolReceptors, AndrogenTestosteroneageingethinylestradiolfemale prostatemale prostateprenatal period

Identifiers

PMID26852889
PMCPMC4840244
OpenAlexW2289952803

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.