Evidence map›Paper›PMID 33807638›Full record

ArticleMolecules (Basel, Switzerland)2021

Signaling Pathways Regulated by Silica Nanoparticles.

Shih-Yi Hsu, Robert Morris, Feng Cheng

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

3 authors.

Shih-Yi HsuDepartment of Pharmaceutical Science, College of Pharmacy, University of South Florida, Tampa, FL 33612, USA.
Robert MorrisDepartment of Pharmaceutical Science, College of Pharmacy, University of South Florida, Tampa, FL 33612, USA.ORCID 0000-0002-6994-0602
Feng ChengDepartment of Pharmaceutical Science, College of Pharmacy, University of South Florida, Tampa, FL 33612, USA.ORCID 0000-0003-3619-8090

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Silica nanoparticles are a class of molecules commonly used in drug or gene delivery systems that either facilitate the delivery of therapeutics to specific drug targets or enable the efficient delivery of constructed gene products into biological systems. Some in vivo or in vitro studies have demonstrated the toxic effects of silica nanoparticles. Despite the availability of risk management tools in response to the growing use of synthetic silica in commercial products, the molecular mechanism of toxicity induced by silica nanoparticles is not well characterized. The purpose of this study was to elucidate the effects of silica nanoparticle exposure in three types of cells including human aortic endothelial cells, mouse-derived macrophages, and A549 non-small cell lung cancer cells using toxicogenomic analysis. The results indicated that among all three cell types, the TNF and MAPK signaling pathways were the common pathways upregulated by silica nanoparticles. These findings may provide insight into the effects of silica nanoparticle exposure in the human body and the possible mechanism of toxicity.

Indexed as

A549 CellsAnimalsCells, CulturedCell SurvivalGene Expression RegulationHumansMacrophagesMAP Kinase Signaling SystemMiceNanoparticlesRAW 264.7 CellsSignal TransductionSilicon DioxideToxicogeneticsTumor Necrosis FactorsSilicon DioxideTumor Necrosis Factorsgene pathwaymechanismmicroarraynanomaterialNCBI GEOsilicon dioxide

Identifiers

PMID33807638
PMCPMC7961477

What OpenQuestion holds

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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.