Evidence map›Paper›PMID 36662064›Full record

ArticleJournal of functional biomaterials2022

Evaluation of the Cytotoxicity of Cationic Polymers on Glioblastoma Cancer Stem Cells.

Conor McCartin, Juliette Blumberger, Candice Dussouillez, Patricia Fernandez de Larrinoa, Monique Dontenwill, Christel Herold-Mende, Philippe Lavalle, Béatrice Heurtault, Stéphane Bellemin-Laponnaz, Sylvie Fournel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of functional biomaterials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
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

11 authors at 3 institutions in 2 countries.

Conor McCartin3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.ORCID 0000-0003-0259-3623
Juliette Blumberger3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
Candice Dussouillez3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.
Patricia Fernandez de Larrinoa3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.ORCID 0000-0002-6597-8187
Monique DontenwillLaboratoire de Bioimagerie et Pathologies UMR CNRS 7021 (LBP), Faculté de Pharmacie, 74 route du Rhin, F-67401 Illkirch, France.ORCID 0000-0002-5235-3014
Christel Herold-MendeDivision of Neurosurgical Research, Department of Neurosurgery, University of Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-1915-745X
Philippe LavalleInstitut National de la Santé et de la Recherche Médicale, Inserm UMR_S 1121 Biomaterials and Bioengineering, F-67085 Strasbourg, France.
Béatrice Heurtault3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.ORCID 0000-0002-8422-9413
Stéphane Bellemin-LaponnazInstitut de Physique et Chimie des Matériaux de Strasbourg (IPCMS) UMR7504, Université de Strasbourg & CNRS 23 rue du Loess, F-67083 Strasbourg, France.ORCID 0000-0001-9462-5703
Sylvie Fournel3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.ORCID 0000-0003-3583-6548
Antoine Kichler3Bio Team, Faculté de Pharmacie, CAMB UMR7199 CNRS-University of Strasbourg, 74 route du Rhin, F-67401 Illkirch, France.ORCID 0000-0003-0593-2424
Centre National de la Recherche Scientifique · FRHeidelberg University · DEInserm · FR

Funding

Agence Nationale de la Recherche ANR-10-IDEX-0002Agence Nationale de la Recherche ANR-20-SFRI-0012Fondation ARC pour la Recherche sur le Cancer ARCPJA32020060002306
6 · The paper itself

Abstract

Cationic polymers such as polyethylenimine (PEI) have found a pervasive place in laboratories across the world as gene delivery agents. However, their applications are not limited to this role, having found a place as delivery agents for drugs, in complexes known as polymer-drug conjugates (PDCs). Yet a potentially underexplored domain of research is in their inherent potential as anti-cancer therapeutic agents, which has been indicated by several studies. Even more interesting is the recent observation that certain polycations may present a significantly greater toxicity towards the clinically important cancer stem cell (CSC) niche than towards more differentiated bulk tumour cells. These cells, which possess the stem-like characteristics of self-renewal and differentiation, are highly implicated in cancer drug resistance, tumour recurrence and poor clinical prognosis. The search for compounds which may target and eliminate these cells is thus of great research interest. As such, the observation in our previous study on a PEI-based PDC which showed a considerably higher toxicity of PEI towards glioblastoma CSCs (GSCs) than on more differentiated glioma (U87) cells led us to investigate other cationic polymers for a similar effect. The evaluation of the toxicity of a range of different types of polycations, and an investigation into the potential source of GSC's sensitivity to such compounds is thus described.

Indexed as

cancer stem cellscationic polymerscytotoxicityglioblastomapolyethylenimine

Identifiers

PMID36662064
PMCPMC9862959
OpenAlexW4312226313

What OpenQuestion holds

Textmetadata
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.