Evidence map›Paper›PMID 31564862›Full record

ArticleInternational journal of nanomedicine2019

Apoptotic and DNA-damaging effects of yttria-stabilized zirconia nanoparticles on human skin epithelial cells.

Fatimah Mohammed Alzahrani, Khadijah Mohammed Saleh Katubi, Daoud Ali, Saud Alarifi

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

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  10. Role of Oxidative Stress in LaInternational journal of nanomedicine · 2021
    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.

Fatimah Mohammed AlzahraniChemistry Department, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Khadijah Mohammed Saleh KatubiChemistry Department, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Daoud AliDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Saud AlarifiDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundYttria-stabilized zirconia (Y

methodsPrior to treatment, the yttria-stabilized zirconia nanoparticles were characterized by using different advanced instruments viz. dynamic light scattering (DLS), scanning electron microscope (SEM) and transmission electron microscope (TEM). Cell viability of HaCaT cells was measured by using MTS and NRU assays and viability of cells was reduced in a dose- and time-dependent manner.

resultsReduction in the viability of cells was correlated with the rise of reactive oxygen species generation, increased caspase-3, mitochondria membrane potential and evidence of DNA strand breakage. These were consistent with the possibility that mitochondria damage can play a significant role in the cytotoxic response. Moreover, the activity of oxidative enzymes such as lipid peroxide (LPO) was increased and glutathione was reduced in HaCaT cells exposed with yttria-stabilized zirconia nanoparticles. It is also important to indicate that HaCaT cells appear to be more susceptible to yttria-stabilized zirconia nanoparticles exposure after 24 hrs.

conclusionThis result provides a dose- and time-dependent apoptosis and genotoxicity of yttria-stabilized zirconia nanoparticles in HaCaT cells.

Indexed as

ApoptosisDNA DamageAcetylcysteineCell LineCell ShapeCell SurvivalDNA Breaks, Double-StrandedDNA FragmentationEpithelial CellsGlutathioneHumansIntracellular MembranesLysosomesMembrane Potential, MitochondrialMetal NanoparticlesOxidative StressAcetylcysteineGlutathioneReactive Oxygen SpeciesyttriaYttriumZirconiumzirconium oxideapoptosisgeno toxicityHaCaT cellsoxidative stressyttria-stabilized zirconia nanoparticles

Identifiers

PMID31564862
PMCPMC6733180

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Registered trials

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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.