Evidence map›Paper›PMID 30763314›Full record

ArticlePLoS genetics2019

Assessing effects of germline exposure to environmental toxicants by high-throughput screening in C. elegans.

Nara Shin, Luciann Cuenca, Rajendiran Karthikraj, Kurunthachalam Kannan, Monica P Colaiácovo

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. High-Throughput Toxicity Screening withEnvironmental science & technology · 2026
    Review
  3. Review
  4. Microplastic-Mediated Delivery of Di-butyl Phthalate AltersMicroplastics (Basel, Switzerland) · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. ADR-2 regulates fertility and oocyte fate inbioRxiv : the preprint server for biology · 2024
    Article
  13. Review
  14. Exploring the Impact ofNutrients · 2023
    Article
  15. Article
  16. Reproductive-Toxicity-Related Endpoints inJournal of developmental biology · 2023
    Article
  17. MutantCancers · 2022
    Article
  18. Article
  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

5 authors at 2 institutions in 1 country.

Nara ShinDepartment of Genetics, Harvard Medical School, Boston, MA, United States of America.
Luciann CuencaDepartment of Genetics, Harvard Medical School, Boston, MA, United States of America.
Rajendiran KarthikrajWadsworth Center, New York State Department of Health, Empire State Plaza, Albany, New York, United States of America.
Kurunthachalam KannanWadsworth Center, New York State Department of Health, Empire State Plaza, Albany, New York, United States of America.
Monica P ColaiácovoDepartment of Genetics, Harvard Medical School, Boston, MA, United States of America.ORCID 0000-0001-7803-4372
Harvard University · USNew York State Department of Health · US

Funding

Synaptonemal Complex Assembly and Function in MeiosisR01GM072551 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Monica P Colaiacovo · 2005 to 2026
$7.5M
NIGMS NIH HHS R01 GM072551
6 · The paper itself

Abstract

Chemicals that are highly prevalent in our environment, such as phthalates and pesticides, have been linked to problems associated with reproductive health. However, rapid assessment of their impact on reproductive health and understanding how they cause such deleterious effects, remain challenging due to their fast-growing numbers and the limitations of various current toxicity assessment model systems. Here, we performed a high-throughput screen in C. elegans to identify chemicals inducing aneuploidy as a result of impaired germline function. We screened 46 chemicals that are widely present in our environment, but for which effects in the germline remain poorly understood. These included pesticides, phthalates, and chemicals used in hydraulic fracturing and crude oil processing. Of the 46 chemicals tested, 41% exhibited levels of aneuploidy higher than those detected for bisphenol A (BPA), an endocrine disruptor shown to affect meiosis, at concentrations correlating well with mammalian reproductive endpoints. We further examined three candidates eliciting aneuploidy: dibutyl phthalate (DBP), a likely endocrine disruptor and frequently used plasticizer, and the pesticides 2-(thiocyanomethylthio) benzothiazole (TCMTB) and permethrin. Exposure to these chemicals resulted in increased embryonic lethality, elevated DNA double-strand break (DSB) formation, activation of p53/CEP-1-dependent germ cell apoptosis, chromosomal abnormalities in oocytes at diakinesis, impaired chromosome segregation during early embryogenesis, and germline-specific alterations in gene expression. This study indicates that this high-throughput screening system is highly reliable for the identification of environmental chemicals inducing aneuploidy, and provides new insights into the impact of exposure to three widely used chemicals on meiosis and germline function.

Indexed as

AneugensAneuploidyAnimalsAnimals, Genetically ModifiedBenzothiazolesCaenorhabditis elegansDibutyl PhthalateDNA Breaks, Double-StrandedDrug Evaluation, PreclinicalEnvironmental ExposureEnvironmental PollutantsGerm CellsHigh-Throughput Screening AssaysInsecticidesMeiosisPermethrin2-(thiocyanomethylthio)benzothiazoleAneugensBenzothiazolesDibutyl PhthalateEnvironmental PollutantsInsecticidesPermethrinPlasticizersThiocyanates

Identifiers

PMID30763314
PMCPMC6375566
OpenAlexW2914824933

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.