Evidence map›Paper›PMID 25709447›Full record

ArticleInternational journal of nanomedicine2015

Targeting and treatment of glioblastomas with human mesenchymal stem cells carrying ferrociphenol lipid nanocapsules.

Anne Clavreul, Angélique Montagu, Anne-Laure Lainé, Clément Tétaud, Nolwenn Lautram, Florence Franconi, Catherine Passirani, Anne Vessières, Claudia N Montero-Menei, Philippe Menei

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
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  6. Review
  7. Review
  8. Mesenchymal stem cells loaded with paclitaxel-poly(lactic-International journal of nanomedicine · 2018
    Article
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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

10 authors.

Anne ClavreulDépartement de Neurochirurgie, Centre Hospitalier Universitaire, Angers, France.
Angélique MontaguINSERM UMR-S 1066, Université d'Angers, LUNAM Université, Angers, France.
Anne-Laure LainéINSERM UMR-S 1066, Université d'Angers, LUNAM Université, Angers, France.
Clément TétaudINSERM UMR-S 1066, Université d'Angers, LUNAM Université, Angers, France.
Nolwenn LautramINSERM UMR-S 1066, Université d'Angers, LUNAM Université, Angers, France.
Florence FranconiCIFAB-PRIMEX, Université d'Angers, LUNAM Université, Angers, France.
Catherine PassiraniINSERM UMR-S 1066, Université d'Angers, LUNAM Université, Angers, France.
Anne VessièresCNRS-UMR 7223, ENSCP, Paris, France.
Claudia N Montero-MeneiINSERM UMR-S 1066, Université d'Angers, LUNAM Université, Angers, France.
Philippe MeneiDépartement de Neurochirurgie, Centre Hospitalier Universitaire, Angers, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently developed drug delivery nanosystems, such as lipid nanocapsules (LNCs), hold great promise for the treatment of glioblastomas (GBs). In this study, we used a subpopulation of human mesenchymal stem cells, "marrow-isolated adult multilineage inducible" (MIAMI) cells, which have endogenous tumor-homing activity, to deliver LNCs containing an organometallic complex (ferrociphenol or Fc-diOH), in the orthotopic U87MG GB model. We determined the optimal dose of Fc-diOH-LNCs that can be carried by MIAMI cells and compared the efficacy of Fc-diOH-LNC-loaded MIAMI cells with that of the free-standing Fc-diOH-LNC system. We showed that MIAMI cells entrapped an optimal dose of about 20 pg Fc-diOH per cell, with no effect on cell viability or migration capacity. The survival of U87MG-bearing mice was longer after the intratumoral injection of Fc-diOH-LNC-loaded MIAMI cells than after the injection of Fc-diOH-LNCs alone. The greater effect of the Fc-diOH-LNC-loaded MIAMI cells may be accounted for by their peritumoral distribution and a longer residence time of the drug within the tumor. These results confirm the potential of combinations of stem cell therapy and nanotechnology to improve the local tissue distribution of anticancer drugs in GB.

Indexed as

Antineoplastic AgentsFerrous CompoundsLipidsMesenchymal Stem Cell TransplantationNanocapsulesAnimalsCell Line, TumorCells, CulturedCell SurvivalGlioblastomaHumansMiceXenograft Model Antitumor AssaysAntineoplastic AgentsferrociphenolFerrous CompoundsLipidsNanocapsulesdrug deliveryglioblastomamesenchymal stem cellsnanoparticletargeting

Identifiers

PMID25709447
PMCPMC4335613

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Registered trials

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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.