Evidence map›Paper›PMID 34602817›Full record

ArticleInternational journal of nanomedicine2021

Specific Binding of Novel SPION-Based System Bearing Anti-N-Cadherin Antibodies to Prostate Tumor Cells.

Karolina Karnas, Tomasz Strączek, Czesław Kapusta, Małgorzata Lekka, Joanna Dulińska-Litewka, Anna Karewicz

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2021. 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Karolina KarnasDepartment of Chemistry, Jagiellonian University, Kraków, Poland.
Tomasz StrączekAGH University of Science and Technology, Faculty of Physics and Applied Computer Science, Department of Solid State Physics, Kraków, Poland.
Czesław KapustaAGH University of Science and Technology, Faculty of Physics and Applied Computer Science, Department of Solid State Physics, Kraków, Poland.
Małgorzata LekkaDepartment of Biophysical Microstructures, Institute of Nuclear Physics, Polish Academy of Sciences, Kraków, Poland.
Joanna Dulińska-LitewkaChair of Medical Biochemistry, Jagiellonian University Medical College, Kraków, Poland.ORCID 0000-0002-6376-496X
Anna KarewiczDepartment of Chemistry, Jagiellonian University, Kraków, Poland.ORCID 0000-0001-9769-6240
Jagiellonian University · PLAGH University of Krakow · PLInstitute of Nuclear Physics, Polish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEpithelial-mesenchymal (EMT) transition plays an important role in metastasis and is accompanied by an upregulation of N-cadherin expression. A new nanoparticulate system (SPION/CCh/N-cad) based on superparamagnetic iron oxide nanoparticles, stabilized with a cationic derivative of chitosan and surface-modified with anti-N-cadherin antibody, was synthetized for the effective capture of N-cadherin expressing circulating tumor cells (CTC).

methodsThe morphology, physicochemical, and magnetic properties of the system were evaluated using dynamic light scattering (DLS), fluorescence spectroscopy, Mössbauer spectroscopy, magnetometry, and fluorescence spectroscopy. Atomic force microscopy (AFM), confocal microscopy and flow cytometry were used to study the interaction of our nanoparticulate system with N-cadherin expressed in prostate cancer cell lines (PC-3 and DU 145). A purpose-built cuvette was used in the cancer cell capture experiments.

resultsThe obtained nanoparticles were a spherical, stable colloid, and exhibited excellent magnetic properties. Biological experiments confirmed that the novel SPION/CCh/N-cad system interacts specifically with N-cadherin present on the cell surface. Preliminary studies on the magnetic capture of PC-3 cells using the obtained nanoparticles were successful. Incubation times as short as 1 minute were sufficient for the synthesized system to effectively bind to the PC-3 cells.

conclusionResults obtained for our system suggest a possibility of using it to capture CTC in the flow conditions.

Indexed as

NanoparticlesProstatic NeoplasmsCadherinsCell Line, TumorHumansMagnetic Iron Oxide NanoparticlesMagneticsMaleCadherinsantibodycancercirculating tumor cellsmagnetic cell captureN-cadherinsuperparamagnetic iron oxide nanoparticles

Identifiers

PMID34602817
PMCPMC8478793
OpenAlexW3204866745

What OpenQuestion holds

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LicenceCC BY-NC
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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.