Evidence map›Paper›PMID 28704436›Full record

ArticlePloS one2017

Platinum nanoparticles induce damage to DNA and inhibit DNA replication.

Lukas Nejdl, Jiri Kudr, Amitava Moulick, Dagmar Hegerova, Branislav Ruttkay-Nedecky, Jaromir Gumulec, Kristyna Cihalova, Kristyna Smerkova, Simona Dostalova, Sona Krizkova and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.8field-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

32 citing papers in PubMed, 76 citations in OpenAlex.

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  16. Nanoparticles in Clinical Translation for Cancer Therapy.International journal of molecular sciences · 2022
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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

13 authors at 1 institution in 1 country.

Lukas NejdlDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Jiri KudrDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Amitava MoulickDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Dagmar HegerovaDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Branislav Ruttkay-NedeckyDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Jaromir GumulecCentral European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
Kristyna CihalovaDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Kristyna SmerkovaDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Simona DostalovaDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Sona KrizkovaDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Marie NovotnaDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Pavel KopelDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.
Vojtech AdamDepartment of Chemistry and Biochemistry, Mendel University in Brno, Brno, Czech Republic.ORCID http://orcid.org/0000-0002-8527-286X
Central European Institute of Technology · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sparsely tested group of platinum nanoparticles (PtNPs) may have a comparable effect as complex platinum compounds. The aim of this study was to observe the effect of PtNPs in in vitro amplification of DNA fragment of phage λ, on the bacterial cultures (Staphylococcus aureus), human foreskin fibroblasts and erythrocytes. In vitro synthesized PtNPs were characterized by dynamic light scattering (PtNPs size range 4.8-11.7 nm), zeta potential measurements (-15 mV at pH 7.4), X-ray fluorescence, UV/vis spectrophotometry and atomic absorption spectrometry. The PtNPs inhibited the DNA replication and affected the secondary structure of DNA at higher concentrations, which was confirmed by polymerase chain reaction, DNA sequencing and DNA denaturation experiments. Further, cisplatin (CisPt), as traditional chemotherapy agent, was used in all parallel experiments. Moreover, the encapsulation of PtNPs in liposomes (LipoPtNPs) caused an approximately 2.4x higher of DNA damage in comparison with CisPt, LipoCisPt and PtNPs. The encapsulation of PtNPs in liposomes also increased their antibacterial, cytostatic and cytotoxic effect, which was determined by the method of growth curves on S. aureus and HFF cells. In addition, both the bare and encapsulated PtNPs caused lower oxidative stress (determined by GSH/GSSG ratio) in the human erythrocytes compared to the bare and encapsulated CisPt. CisPt was used in all parallel experiments as traditional chemotherapy agent.

Indexed as

DNA DamageDNA ReplicationCell LineCells, CulturedErythrocytesFibroblastsHumansMetal NanoparticlesOxidative StressPlatinumStaphylococcus aureusPlatinum

Identifiers

PMID28704436
PMCPMC5507526
OpenAlexW2735460356

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.