Evidence map›Paper›PMID 34829821›Full record

ArticleBiomedicines2021

Targeting Brain Tumors with Mesenchymal Stem Cells in the Experimental Model of the Orthotopic Glioblastoma in Rats.

Natalia Yudintceva, Ekaterina Lomert, Natalia Mikhailova, Elena Tolkunova, Nikol Agadzhanian, Konstantin Samochernych, Gabriele Multhoff, Grigoriy Timin, Vyacheslav Ryzhov, Vladimir Deriglazov and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

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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

12 authors at 7 institutions in 3 countries.

Natalia YudintcevaInstitute of Cytology of the Russian Academy of Sciences (RAS), 194064 St. Petersburg, Russia.ORCID 0000-0002-7357-1571
Ekaterina LomertInstitute of Cytology of the Russian Academy of Sciences (RAS), 194064 St. Petersburg, Russia.
Natalia MikhailovaInstitute of Cytology of the Russian Academy of Sciences (RAS), 194064 St. Petersburg, Russia.ORCID 0000-0003-1650-9330
Elena TolkunovaInstitute of Cytology of the Russian Academy of Sciences (RAS), 194064 St. Petersburg, Russia.ORCID 0000-0003-1254-2619
Nikol AgadzhanianInstitute of Cytology of the Russian Academy of Sciences (RAS), 194064 St. Petersburg, Russia.
Konstantin SamochernychPersonalized Medicine Centre, Almazov National Medical Research Centre, Polenov Russian Scientific, Research Institute of Neurosurgery, 197341 St. Petersburg, Russia.
Gabriele MulthoffCentral Institute for Translational Cancer Research (TranslaTUM), Department of Radiation Oncology, Klinikum Rechts der Isar, Technical University of Munich, 81675 Munich, Germany.
Grigoriy TiminInstitute of Cytology of the Russian Academy of Sciences (RAS), 194064 St. Petersburg, Russia.
Vyacheslav RyzhovPetersburg Nuclear Physics Institute Named by B.P.Konstantinov of National Research Center "Kurchatov Institute", 188300 Gatchina, Russia.ORCID 0000-0002-0546-1805
Vladimir DeriglazovPetersburg Nuclear Physics Institute Named by B.P.Konstantinov of National Research Center "Kurchatov Institute", 188300 Gatchina, Russia.ORCID 0000-0002-1315-9008
Anton MazurMagnetic Resonance Research Center, Saint-Petersburg State University, 199034 St. Petersburg, Russia.ORCID 0000-0002-2746-6762
Maxim ShevtsovInstitute of Cytology of the Russian Academy of Sciences (RAS), 194064 St. Petersburg, Russia.ORCID 0000-0002-8539-2239
Institute of Cytology · RUFederal Almazov North-West Medical Research Centre · RUPetersburg Nuclear Physics Institute · RUTUM Klinikum · DEITMO University · RUSt Petersburg University · RUUniversity of Geneva · CH

Funding

DFG with grant number (SFB824/3, STA1520/1-1), program Open Access Publishing. DFG SFB824/3, STA1520/1-1
6 · The paper itself

Abstract

Despite multimodal approaches for the treatment of multiforme glioblastoma (GBM) advances in outcome have been very modest indicating the necessity of novel diagnostic and therapeutic strategies. Currently, mesenchymal stem cells (MSCs) represent a promising platform for cell-based cancer therapies because of their tumor-tropism, low immunogenicity, easy accessibility, isolation procedure, and culturing. In the present study, we assessed the tumor-tropism and biodistribution of the superparamagnetic iron oxide nanoparticle (SPION)-labeled MSCs in the orthotopic model of C6 glioblastoma in Wistar rats. As shown in in vitro studies employing confocal microscopy, high-content quantitative image cytometer, and xCelligence system MSCs exhibit a high migratory capacity towards C6 glioblastoma cells. Intravenous administration of SPION-labeled MSCs in vivo resulted in intratumoral accumulation of the tagged cells in the tumor tissues that in turn significantly enhanced the contrast of the tumor when high-field magnetic resonance imaging was performed. Subsequent biodistribution studies employing highly sensitive nonlinear magnetic response measurements (

Indexed as

biodistributionC6 gliomamagnetic resonance imagingmesenchymal stem cellsmultiforme glioblastomanonlinear magnetic responsesuperparamagnetic iron oxide nanoparticlestargeted drug delivery

Identifiers

PMID34829821
PMCPMC8615766
OpenAlexW3210646567

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.