Evidence map›Paper›PMID 23892599›Full record

ArticleInternational journal of molecular sciences2013

Effects of Fe3O4 Magnetic Nanoparticles on A549 Cells.

Masatoshi Watanabe, Misao Yoneda, Ayaka Morohashi, Yasuki Hori, Daiki Okamoto, Akiko Sato, Daisuke Kurioka, Tadashi Nittami, Yoshifumi Hirokawa, Taizo Shiraishi and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
  2. In Vitro Antitumor Effects of Melittin Attached to FeMolecules (Basel, Switzerland) · 2026
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  3. Genotoxicity assessment of mesoporous silica and graphene oxide in GDL1 cells.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2025
    Article
  4. Magnetic Hydrogels as a Treatment for Oncological Pathologies.Journal of functional biomaterials · 2025
    Review
  5. Review
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  7. Inhaled Nanoparticulate Systems: Composition, Manufacture and Aerosol Delivery.Journal of aerosol medicine and pulmonary drug delivery · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Fabrication of α-FeACS omega · 2022
    Article
  12. Toxicological Aspects of Iron Oxide Nanoparticles.Advances in experimental medicine and biology · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review of Curcumin Physicochemical Targeting Delivery System.International journal of nanomedicine · 2020
    Review
  20. 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

13 authors at 4 institutions in 2 countries.

Masatoshi WatanabeLaboratory for Medical Engineering, Division of Materials and Chemical Engineering, Graduate School of Engineering, Yokohama National University, Yokohama 240-8501, Japan. mawata@ynu.ac.jp
Misao Yoneda
Ayaka Morohashi
Yasuki Hori
Daiki Okamoto
Akiko Sato
Daisuke Kurioka
Tadashi Nittami
Yoshifumi Hirokawa
Taizo Shiraishi
Kazuaki Kawai
Hiroshi Kasai
Yukari Totsuka
Yokohama National University · JPMie University · JPUniversity of Occupational and Environmental Health Japan · JPNational Cancer Research Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fe3O4 magnetic nanoparticles (MgNPs-Fe3O4) are widely used in medical applications, including magnetic resonance imaging, drug delivery, and in hyperthermia. However, the same properties that aid their utility in the clinic may potentially induce toxicity. Therefore, the purpose of this study was to investigate the cytotoxicity and genotoxicity of MgNPs-Fe3O4 in A549 human lung epithelial cells. MgNPs-Fe3O4 caused cell membrane damage, as assessed by the release of lactate dehydrogenase (LDH), only at a high concentration (100 μg/mL); a lower concentration (10 μg/mL) increased the production of reactive oxygen species, increased oxidative damage to DNA, and decreased the level of reduced glutathione. MgNPs-Fe3O4 caused a dose-dependent increase in the CD44+ fraction of A549 cells. MgNPs-Fe3O4 induced the expression of heme oxygenase-1 at a concentration of 1 μg/mL, and in a dose-dependent manner. Despite these effects, MgNPs-Fe3O4 had minimal effect on cell viability and elicited only a small increase in the number of cells undergoing apoptosis. Together, these data suggest that MgNPs-Fe3O4 exert little or no cytotoxicity until a high exposure level (100 μg/mL) is reached. This dissociation between elevated indices of cell damage and a small effect on cell viability warrants further study.

Indexed as

ApoptosisCell LineCell MembraneCell SurvivalDNA DamageEpithelial CellsFerric CompoundsGlutathioneHeme Oxygenase-1HumansHyaluronan ReceptorsL-Lactate DehydrogenaseMagnetite NanoparticlesMutagenicity TestsOxidation-ReductionOxidative StressFerric Compoundsferric oxideGlutathioneHeme Oxygenase-1Hyaluronan ReceptorsL-Lactate DehydrogenaseMagnetite NanoparticlesReactive Oxygen Species

Identifiers

PMID23892599
PMCPMC3759872
OpenAlexW2091666566

What OpenQuestion holds

Textmetadata
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.