Evidence map›Paper›PMID 29181062›Full record

ArticleArchives of medical science : AMS2017

Investigation of platinum nanoparticle properties against U87 glioblastoma multiforme.

Marta Kutwin, Ewa Sawosz, Slawomir Jaworski, Mateusz Hinzmann, Mateusz Wierzbicki, Anna Hotowy, Marta Grodzik, Anna Winnicka, Andre Chwalibog

Open access · goldAbstract read
In one paragraph

Article in Archives of medical science : AMS, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 56 citations in OpenAlex.

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  11. Review
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  19. Review
  20. Mechanism of microRNA-431-5p-Archives of medical science : AMS · 2019
    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

9 authors at 2 institutions in 2 countries.

Marta KutwinDepartment of Animal Sciences, Warsaw University of Life Sciences, Warsaw, Poland.
Ewa SawoszDivision of Biotechnology and Biochemistry of Nutrition, Faculty of Animal Science, Warsaw University of Life Science, Warsaw, Poland.
Slawomir JaworskiDivision of Biotechnology and Biochemistry of Nutrition, Faculty of Animal Science, Warsaw University of Life Science, Warsaw, Poland.
Mateusz HinzmannDivision of Biotechnology and Biochemistry of Nutrition, Faculty of Animal Science, Warsaw University of Life Science, Warsaw, Poland.
Mateusz WierzbickiDivision of Biotechnology and Biochemistry of Nutrition, Faculty of Animal Science, Warsaw University of Life Science, Warsaw, Poland.
Anna HotowyDivision of Biotechnology and Biochemistry of Nutrition, Faculty of Animal Science, Warsaw University of Life Science, Warsaw, Poland.
Marta GrodzikDivision of Biotechnology and Biochemistry of Nutrition, Faculty of Animal Science, Warsaw University of Life Science, Warsaw, Poland.
Anna WinnickaDepartment of Pathology and Veterinary Diagnostics, Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Warsaw, Poland.
Andre ChwalibogDepartment of Veterinary Clinical and Animal Sciences, University of Copenhagen, Copenhagen, Denmark.
Warsaw University of Life Sciences · PLUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGliomas are the most aggressive and common primary tumors of the central nervous system (CNS). Many side effects of drugs containing platinum and their poor penetration of the CNS are major drawbacks in glioma therapy. The aim of the study was to investigate and compare the toxicity of platinum nanoparticles and cisplatin and their anticancer properties in examination with a U87 glioma cell line and tumor. MATERIAL AND

methodsNanoparticles of platinum (NP-Pt) and cisplatin were incubated with U87 glioma cells or injected directly into tumor tissue. The biological properties of NP-Pt and cisplatin were compared through the morphology, viability, mortality, genotoxicity and the type of cell death of U87 glioma cells, the morphology and ultrastructure of glioma tumor, and expression of caspase-3, p53 and PCNA mRNA.

resultsNP-Pt at concentrations of 0.14 µM/ml, 0.29 µM/ml and 0.65 µM/ml had a harmful influence on viability of U87 glioblastoma multiforme (GBM) cells, but also showed genotoxic properties as well as a pro-apoptotic effect on cancer cells. It was found that NP-Pt decreased the weight and volume of U87 GBM tumor tissue and caused pathomorphological changes in the ultrastructure and morphology of tumor tissue, but they also upregulated

conclusionsThe comparison between the effectiveness of glioblastoma treatment by NP-Pt vs cisplatin showed promising results for future studies. The results indicate that the properties of NP-Pt might be utilized for brain cancer therapy.

Indexed as

apoptosiscancergenotoxicityglioblastomaplatinum nanoparticlesU87

Identifiers

PMID29181062
PMCPMC5701677
OpenAlexW2400821311

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.