Evidence map›Paper›PMID 30889203›Full record

ArticlePloS one2019

Nano-mediated delivery of double-stranded RNA for gene therapy of glioblastoma multiforme.

Małgorzata Grabowska, Bartosz F Grześkowiak, Kosma Szutkowski, Dariusz Wawrzyniak, Paweł Głodowicz, Jan Barciszewski, Stefan Jurga, Katarzyna Rolle, Radosław Mrówczyński

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-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

17 citing papers in PubMed, 39 citations in OpenAlex.

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  3. The role of TNC in atherosclerosis and drug development opportunities.International journal of biological sciences · 2024
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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

9 authors at 2 institutions in 1 country.

Małgorzata GrabowskaDepartment of Molecular Neurooncology, Institute of Bioorganic Chemistry Polish Academy of Science, Poznan, Poland.
Bartosz F GrześkowiakNanoBioMedical Centre, Adam Mickiewicz University in Poznan, Poznan, Poland.
Kosma SzutkowskiNanoBioMedical Centre, Adam Mickiewicz University in Poznan, Poznan, Poland.
Dariusz WawrzyniakDepartment of Molecular Neurooncology, Institute of Bioorganic Chemistry Polish Academy of Science, Poznan, Poland.
Paweł GłodowiczDepartment of Molecular Neurooncology, Institute of Bioorganic Chemistry Polish Academy of Science, Poznan, Poland.
Jan BarciszewskiDepartment of Epigenetics, Institute of Bioorganic Chemistry Polish Academy of Science, Poznan, Poland.
Stefan JurgaNanoBioMedical Centre, Adam Mickiewicz University in Poznan, Poznan, Poland.
Katarzyna RolleDepartment of Molecular Neurooncology, Institute of Bioorganic Chemistry Polish Academy of Science, Poznan, Poland.
Radosław MrówczyńskiNanoBioMedical Centre, Adam Mickiewicz University in Poznan, Poznan, Poland.ORCID 0000-0003-3687-911X
Institute of Bioorganic Chemistry, Polish Academy of Sciences · PLAdam Mickiewicz University in Poznań · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most common type of malignant gliomas, characterized by genetic instability, intratumoral histopathological variability and unpredictable clinical behavior. Disappointing results in the treatment of gliomas with surgery, radiation and chemotherapy have fueled a search for new therapeutic targets and treatment modalities. Here we report new approach towards RNA interference therapy of glioblastoma multiforme based on the magnetic nanoparticles delivery of the double-stranded RNA (dsRNA) with homological sequences to mRNA of tenascin-C (TN-C), named ATN-RNA. The obtained nanocomposite consisted of polyethyleneimine (PEI) coated magnetic nanoparticles conjugated to the dsRNA show high efficiency in ATN-RNA delivery, resulting not only in significant TN-C expression level suppressesion, but also impairing the tumor cells migration. Moreover, synthesized nanomaterials show high contrast properties in magnetic resonance imaging (MRI) and low cytotoxicity combining with lack of induction of interferon response. We believe that the present work is a successful combination of effective, functional, non-immunostimulatory dsRNA delivery system based on magnetic nanoparticles with high potential for further application in GBM therapy.

Indexed as

Brain NeoplasmsCell Line, TumorCell MovementCell ProliferationGenetic TherapyGlioblastomaHumansMagnetic Resonance ImagingMagnetite NanoparticlesPolyethyleneimineRNA, Double-StrandedRNA InterferenceRNA, MessengerRNA, Small InterferingTenascinTransfectionMagnetite NanoparticlesPolyethyleneimineRNA, Double-StrandedRNA, MessengerRNA, Small InterferingTenascin

Identifiers

PMID30889203
PMCPMC6424419
OpenAlexW2925143807

What OpenQuestion holds

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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.