Evidence map›Paper›PMID 31318015›Full record

ArticleBiology of reproduction2019

Environmentally relevant exposure to dibutyl phthalate disrupts DNA damage repair gene expression in the mouse ovary†.

Xiaosong Liu, Zelieann R Craig

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
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  4. Prenatal exposure to environmentally relevant low-dosage dibutyl phthalate reduces placental efficiency in CD-1 mice.Toxicological sciences : an official journal of the Society of Toxicology · 2025
    Article
  5. Review
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  8. Article
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  10. Article
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  13. Review
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  15. Article
  16. Article
  17. The effects of plasticizers on the ovary.Current opinion in endocrine and metabolic research · 2021
    Article
  18. Review
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Xiaosong LiuSchool of Animal & Comparative Biomedical Sciences, The University of Arizona, Tucson, Arizona, USA.
Zelieann R CraigSchool of Animal & Comparative Biomedical Sciences, The University of Arizona, Tucson, Arizona, USA.
University of Arizona · US

Funding

SOUTHWEST ENVIRONMENTAL HEALTH SCIENCES CENTERP30ES006694 · NIEHS · UNIVERSITY OF ARIZONA · PI DEAN BILLHEIMER · 1994 to 2026
$36.7M
Environmentally Relevant Phthalate Exposures and Ovarian FunctionR01ES026998 · NIEHS · UNIVERSITY OF ARIZONA · PI CRAIG, ZELIEANN RIVERA · 2017 to 2021
$2.5M
Mechanisms of phthalate-induced ovarian follicle toxicityR00ES021467 · NIEHS · UNIVERSITY OF ARIZONA · PI CRAIG, ZELIEANN RIVERA · 2013 to 2015
$731k
NIEHS NIH HHS P30 ES006694NIEHS NIH HHS R00 ES021467NIEHS NIH HHS R01 ES026998
6 · The paper itself

Abstract

Phthalates have a history of reproductive toxicity in animal models and associations with adverse reproductive outcomes in women. Human exposure to dibutyl phthalate (DBP) occurs via consumer products (7-10 μg/kg/day) and medications (1-233 μg/kg/day). Most DBP toxicity studies have focused on high supraphysiological exposure levels; thus, very little is known about exposures occurring at environmentally relevant levels. CD-1 female mice (80 days old) were treated with tocopherol-stripped corn oil (vehicle control) or DBP dissolved in oil at environmentally relevant (10 and 100 μg/kg/day) or higher (1000 μg/kg/day) levels for 30 days to evaluate effects on DNA damage response (DDR) pathway genes and folliculogenesis. DBP exposure caused dose-dependent effects on folliculogenesis and gene expression. Specifically, animals exposed to the high dose of DBP had more atretic follicles in their ovaries, while in those treated with environmentally relevant doses, follicle numbers were no different from vehicle-treated controls. DBP exposure significantly reduced the expression of DDR genes including those involved in homologous recombination (Atm, Brca1, Mre11a, Rad50), mismatch repair (Msh3, Msh6), and nucleotide excision repair (Xpc, Pcna) in a dose-specific manner. Interestingly, staining for the DNA damage marker, γH2AX, was similar between treatments. DBP exposure did not result in differential DNA methylation in the Brca1 promoter but significantly reduced transcript levels for the maintenance DNA methyltransferase, Dnmt1, in the ovary. Collectively, these findings show that oral exposure to environmentally relevant levels of DBP for 30 days does not significantly impact folliculogenesis in adult mice but leads to aberrant ovarian expression of DDR genes.

Indexed as

AnimalsDibutyl PhthalateDNA DamageDNA RepairEndocrine DisruptorsEnvironmental ExposureEnvironmental PollutantsEstrous CycleFemaleGene Expression RegulationMiceMutS Homolog 3 ProteinOvaryDibutyl PhthalateEndocrine DisruptorsEnvironmental PollutantsMsh3 protein, mouseMutS Homolog 3 Proteinatresiacell cycleendocrine disruptorsenvironmental contaminants and toxicantsfolliclefollicle developmentfollicle maturationgene expressionovaryphthalaterodentstoxicology

Identifiers

PMID31318015
PMCPMC6930367
OpenAlexW2963475001

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.