Evidence map›Paper›PMID 31792261›Full record

ArticleScientific reports2019

Genetic and epigenetic alterations induced by bisphenol A exposure during different periods of spermatogenesis: from spermatozoa to the progeny.

Marta Lombó, Cristina Fernández-Díez, Silvia González-Rojo, María Paz Herráez

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  5. Article
  6. Review
  7. How Early-Life Programming During Embryogenesis Imprints Cellular Memory.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Article
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  12. Perspective in the Mechanisms for Repairing Sperm DNA Damage.Reproductive sciences (Thousand Oaks, Calif.) · 2025
    Review
  13. Article
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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

4 authors at 2 institutions in 1 country.

Marta LombóDepartment of Molecular Biology, Faculty of Biology and Environmental Sciences, Universidad de León, Campus de Vegazana, León, 24071, Spain.
Cristina Fernández-DíezInstituto Ganadero de Motaña (IGM), Finca Marzanas-Grulleros Vega de Infanzones, León, 24346, Spain.
Silvia González-RojoDepartment of Molecular Biology, Faculty of Biology and Environmental Sciences, Universidad de León, Campus de Vegazana, León, 24071, Spain.
María Paz HerráezDepartment of Molecular Biology, Faculty of Biology and Environmental Sciences, Universidad de León, Campus de Vegazana, León, 24071, Spain. paz.herraez@unileon.es.
Universidad de León · ESInstituto de Ganadería de Montaña · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exposure to bisphenol A (BPA) has been related to male reproductive disorders. Since this endocrine disruptor also displays genotoxic and epigenotoxic effects, it likely alters the spermatogenesis, a process in which both hormones and chromatin remodeling play crucial roles. The hypothesis of this work is that BPA impairs early embryo development by modifying the spermatic genetic and epigenetic information. Zebrafish males were exposed to 100 and 2000 μg/L BPA during early spermatogenesis and during the whole process. Genotoxic and epigenotoxic effects on spermatozoa (comet assay and immunocytochemistry) as well as progeny development (mortality, DNA repairing activity, apoptosis and epigenetic profile) were evaluated. Exposure to 100 µg/L BPA during mitosis slightly increased sperm chromatin fragmentation, enhancing DNA repairing activity in embryos. The rest of treatments promoted high levels of sperm DNA damage, triggering apoptosis in early embryo and severely impairing survival. Regarding epigenetics, histone acetylation (H3K9Ac and H3K27Ac) was similarly enhanced in spermatozoa and embryos from males exposed to all the treatments. Therefore, BPA male exposure jeopardizes embryonic survival and development due to the transmission of a paternal damaged genome and of a hyper-acetylated histone profile, both alterations depending on the dose of the toxicant and the temporal window of exposure.

Indexed as

AcetylationAnimalsBenzhydryl CompoundsBisphenol A CompoundsChromatinDNA RepairEmbryonic DevelopmentEmbryo, NonmammalianEndocrine DisruptorsEpigenesis, GeneticHistonesMaleModels, AnimalPhenolsSpermatogenesisSpermatozoaBenzhydryl Compoundsbisphenol ABisphenol A CompoundsChromatinEndocrine DisruptorsHistonesPhenols

Identifiers

PMID31792261
PMCPMC6889327
OpenAlexW2990597010

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.