Evidence map›Paper›PMID 23777334›Full record

ArticleBioconjugate chemistry2013

Inducing cancer cell death by targeting its nucleus: solid gold nanospheres versus hollow gold nanocages.

Megan A Mackey, Farhat Saira, Mahmoud A Mahmoud, Mostafa A El-Sayed

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Plasmonic Nanoparticles: Advanced Researches (II).Advances in experimental medicine and biology · 2021
    Article
  7. Article
  8. Gold Nanoparticles as Radiosensitizers in Cancer Radiotherapy.International journal of nanomedicine · 2020
    Review
  9. Article
  10. Metal-basedTheranostics · 2018
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Nanotechnology in dentistry: prevention, diagnosis, and therapy.International journal of nanomedicine · 2015
    Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Megan A MackeyLaser Dynamics Laboratory, School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia, United States.
Farhat Saira
Mahmoud A Mahmoud
Mostafa A El-Sayed
Georgia Institute of Technology · US

Funding

Toxicity and Efficacy of Gold Nanoparticle Photothermal Therapy in CancerU01CA151802 · NCI · EMORY UNIVERSITY · PI EL-SAYED, MOSTAFA A, SHIN, DONG M · 2010 to 2014
$2.1M
NCI NIH HHS U01 CA151802NCI NIH HHS U01CA151802-01
6 · The paper itself

Abstract

Recently, we have shown that targeting the cancer cell nucleus with solid gold nanospheres, using a cancer cell penetrating/pro-apoptotic peptide (RGD) and a nuclear localization sequence peptide (NLS), inhibits cell division, thus leading to apoptosis. In the present work, flow cytometric analysis revealed an increase in cell death, via apoptosis and necrosis, in HSC cells upon treatment with peptide-conjugated hollow gold nanocages, compared to those treated with the peptide-conjugated solid gold nanospheres. This is consistent with a G0/G1 phase accumulation, S phase depletion, and G2/M phase depletion, as well as reduced ATP levels. Here, we investigate the possible causes for the observed enhanced cell death with the use of confocal microscopy. The fluorescence images of HSC cells treated with gold nanocages indicate the presence of reactive oxygen species, known to cause apoptosis. The formation of reactive oxygen species observed is consistent with a mechanism involving the oxidation of metallic silver on the inner cavity of the nanocage (inherent to the synthesis of the gold nanocages) to silver oxide. This oxidation is confirmed by an observed redshift in the surface plasmon resonance of the gold nanocages in cell culture medium. The silver oxide, a semiconductor known to photochemically generate hydroxyl radicals, a form of reactive oxygen species, is proposed as a mechanism for the enhanced cell death caused by gold nanocages. Thus, the enhanced cell death, via apoptosis and necrosis, observed with peptide-conjugated hollow gold nanocage-treated cells is considered to be a result of the metallic composition (silver remaining on the inner cavity) of the nanocage.

Indexed as

Antineoplastic AgentsCarcinoma, Squamous CellCell CycleCell DeathCells, CulturedDose-Response Relationship, DrugDrug Screening Assays, AntitumorGoldHumansMetal NanoparticlesMouth NeoplasmsOrganometallic CompoundsParticle SizePeptidesPorosityStructure-Activity RelationshipAntineoplastic AgentsGoldOrganometallic CompoundsPeptides

Identifiers

PMID23777334
PMCPMC3910495
OpenAlexW2056908636

What OpenQuestion holds

Textmetadata
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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.