Evidence map›Paper›PMID 30051916›Full record

ArticleEuropean journal of oral sciences2018

Dose- and time-dependent effects of triethylene glycol dimethacrylate on the proteome of human THP-1 monocytes.

Bo W Nilsen, Jaione Simon-Santamaria, Ulf Örtengren, Einar Jensen, Jack-Ansgar Bruun, Vibeke B Michelsen, Karen K Sørensen

Open access · hybridAbstract read
In one paragraph

Article in European journal of oral sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Biological aspects of modern dental composites.Biomaterial investigations in dentistry · 2023
    Review
  6. Article
  7. Article
  8. 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

7 authors at 2 institutions in 2 countries.

Bo W NilsenDepartment of Clinical Dentistry, UiT - The Arctic University of Norway, Tromsø, Norway.ORCID 0000-0003-3741-7929
Jaione Simon-SantamariaDepartment of Medical Biology, UiT - The Arctic University of Norway, Tromsø, Norway.
Ulf ÖrtengrenDepartment of Clinical Dentistry, UiT - The Arctic University of Norway, Tromsø, Norway.
Einar JensenDepartment of Pharmacy, UiT The Arctic University of Norway, Tromsø, Norway.
Jack-Ansgar BruunDepartment of Medical Biology, UiT - The Arctic University of Norway, Tromsø, Norway.
Vibeke B MichelsenDepartment of Clinical Dentistry, University of Bergen, Bergen, Norway.
Karen K SørensenDepartment of Medical Biology, UiT - The Arctic University of Norway, Tromsø, Norway.
UiT The Arctic University of Norway · NOUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triethylene glycol dimethacrylate (TEGDMA) is commonly used in polymer resin-based dental materials. This study investigated the molecular mechanisms of TEGDMA toxicity by identifying its time- and dose-dependent effects on the proteome of human THP-1 monocytes. The effects of different concentrations (0.07-5 mM) and exposure times (0-72 h) of TEGDMA on cell viability, proliferation, and morphology were determined using a real-time viability assay, automated cell counting, and electron microscopy, and laid the fundament for choice of exposure scenarios in the proteomic experiments. Solvents were not used, as TEGDMA is soluble in cell culture medium (determined by photon correlation spectroscopy). Cells were metabolically labeled [using the stable isotope labeled amino acids in cell culture (SILAC) strategy], and exposed to 0, 0.3 or 2.5 mM TEGDMA for 6 or 16 h before liquid chromatography-tandem mass spectrometry (LC-MS/MS) analyses. Regulated proteins were analyzed in the STRING database. Cells exposed to 0.3 mM TEGDMA showed increased viability and time-dependent upregulation of proteins associated with stress/oxidative stress, autophagy, and cytoprotective functions. Cells exposed to 2.5 mM TEGDMA showed diminished viability and a protein expression profile associated with oxidative stress, DNA damage, mitochondrial dysfunction, and cell cycle inhibition. Altered expression of immune genes was observed in both groups. The study provides novel knowledge about TEGDMA toxicity at the proteomic level. Of note, even low doses of TEGDMA induced a substantial cellular response.

Indexed as

ProteomeCell Culture TechniquesCell CycleCell ProliferationCell SurvivalChromatography, LiquidDental MaterialsDNA DamageDose-Response Relationship, DrugHumansMaterials TestingMitochondriaMonocytesOxidative StressPolyethylene GlycolsPolymethacrylic AcidsDental MaterialsPolyethylene GlycolsPolymethacrylic AcidsProteomeReactive Oxygen SpeciesSolventstriethylene glycol dimethacrylateisotope labelingproteomicsreactive oxygen speciestandem mass spectroscopytriethylene glycol dimethacrylate

Identifiers

PMID30051916
PMCPMC6585793
OpenAlexW2883656188

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.