Evidence map›Paper›PMID 26090418›Full record

ArticleBioMed research international2015

Effect of Fe3O4 Nanoparticles on Skin Tumor Cells and Dermal Fibroblasts.

Lirija Alili, Swetlana Chapiro, Gernot U Marten, Annette M Schmidt, Klaus Zanger, Peter Brenneisen

Abstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Cutaneous Evaluation of FeInternational journal of nanomedicine · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Modifying the tumor microenvironment using nanoparticle therapeutics.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2016
    Review
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

6 authors.

Lirija AliliInstitute of Biochemistry & Molecular Biology I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Swetlana ChapiroInstitute of Biochemistry & Molecular Biology I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Gernot U MartenDepartment of Chemistry, Institute of Physical Chemistry, University of Cologne, 50939 Cologne, Germany.
Annette M SchmidtDepartment of Chemistry, Institute of Physical Chemistry, University of Cologne, 50939 Cologne, Germany.
Klaus ZangerInstitute of Anatomy II, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Peter BrenneisenInstitute of Biochemistry & Molecular Biology I, Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Iron oxide (Fe3O4) nanoparticles have been used in many biomedical approaches. The toxicity of Fe3O4 nanoparticles on mammalian cells was published recently. Though, little is known about the viability of human cells after treatment with Fe3O4 nanoparticles. Herein, we examined the toxicity, production of reactive oxygen species, and invasive capacity after treatment of human dermal fibroblasts (HDF) and cells of the squamous tumor cell line (SCL-1) with Fe3O4 nanoparticles. These nanoparticles had an average size of 65 nm. Fe3O4 nanoparticles induced oxidative stress via generation of reactive oxygen species (ROS) and subsequent initiation of lipid peroxidation. Furthermore, the question was addressed of whether Fe3O4 nanoparticles affect myofibroblast formation, known to be involved in tumor invasion. Herein, Fe3O4 nanoparticles prevent the expression alpha-smooth muscle actin and therefore decrease the number of myofibroblastic cells. Moreover, our data show in vitro that concentrations of Fe3O4 nanoparticles, which are nontoxic for normal cells, partially reveal a ROS-triggered cytotoxic but also a pro-invasive effect on the fraction of squamous cancer cells surviving the treatment with Fe3O4 nanoparticles. The data herein show that the Fe3O4 nanoparticles appear not to be adequate for use in therapeutic approaches against cancer cells, in contrast to recently published data with cerium oxide nanoparticles.

Indexed as

ApoptosisCell Line, TumorFerric CompoundsFibroblastsHumansLipid PeroxidationMetal NanoparticlesOxidative StressReactive Oxygen SpeciesSkinFerric Compoundsferric oxideReactive Oxygen Species

Identifiers

PMID26090418
PMCPMC4454731

What OpenQuestion holds

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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.