Evidence map›Paper›PMID 27992464›Full record

ArticlePloS one2016

Regulation of mRNA Translation Is a Novel Mechanism for Phthalate Toxicity.

Jun Ling, Zenaida P Lopez-Dee, Colby Cottell, Laura Wolfe, Derek Nye

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Single-cell RNA-seq reveals that granulosa cells are a target of phthalate toxicity in the ovary.Toxicological sciences : an official journal of the Society of Toxicology · 2025
    Article
  3. Review
  4. Review
  5. 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 3 institutions in 1 country.

Jun LingDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, Pennsylvania, United States of America.
Zenaida P Lopez-DeeDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, Pennsylvania, United States of America.
Colby CottellDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, Pennsylvania, United States of America.
Laura WolfeDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, Pennsylvania, United States of America.
Derek NyeDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, Pennsylvania, United States of America.
Commonwealth Medical College · USMarywood University · USWilkes University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phthalates are a group of plasticizers that are widely used in many consumer products and medical devices, thus generating a huge burden to human health. Phthalates have been known to cause a number of developmental and reproductive disorders functioning as endocrine modulators. They are also involved in carcinogenesis with mechanisms less understood. To further understand the molecular mechanisms of phthalate toxicity, in this study we reported a new effect of phthalates on mRNA translation/protein synthesis, a key regulatory step of gene expression. Butyl benzyl phthalate (BBP) was found to directly inhibit mRNA translation in vitro but showed a complicated pattern of affecting mRNA translation in cells. In human kidney embryonic cell (HEK-293T), BBP increased cap-dependent mRNA translation at lower concentrations but showed inhibitory effect at higher concentrations. Cap-independent translation was not affected. On the other hand, mono (2-ethylhexyl) phthalate (MEHP) as a major metabolite of another important phthalate di (2-ethylhexyl) phthalate (DEHP) inhibited both can-dependent and -independent mRNA translation in vivo. In contrast, BBP and MEHP exhibited an overall promoting effect on mRNA translation in cancer cells. Mechanistic studies identified that the level and phosphorylation of eIF4E-BP (eIF4E binding protein) and the amount of eIF4GI in eIF4F complex were altered in accordance with the effect of BBP on translation. BBP was also identified to directly bind to eIF4E, providing a further mechanism underlying the regulation of mRNA by phthalate. At the cellular level BBP inhibited normal cell growth but slightly promoted cancer cells (HT29) growth. Overall, this study provides the first evidence that phthalates can directly regulate mRNA translation as a novel mechanism to mediate their biological toxicities.

Indexed as

Cell SurvivalDiethylhexyl PhthalateDose-Response Relationship, DrugEukaryotic Initiation FactorsGene Expression RegulationHEK293 CellsHT29 CellsHumansPhthalic AcidsProtein BiosynthesisRNA CapsRNA, Messengerbutylbenzyl phthalateDiethylhexyl PhthalateEukaryotic Initiation FactorsPhthalic AcidsRNA CapsRNA, Messenger

Identifiers

PMID27992464
PMCPMC5167351
OpenAlexW2561305719

What OpenQuestion holds

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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.