Effects of Dendrimer-microRNA Nanoformulations against Glioblastoma Stem Cells

Author:

Knauer Nadezhda12ORCID,Meschaninova Mariya3ORCID,Muhammad Sajjad2,Hänggi Daniel2,Majoral Jean-Pierre4,Kahlert Ulf Dietrich5ORCID,Kozlov Vladimir1,Apartsin Evgeny K.6ORCID

Affiliation:

1. Research Institute of Fundamental and Clinical Immunology, 630099 Novosibirsk, Russia

2. Clinic for Neurosurgery, Medical Faculty, Heinrich-Heine University Medical Center Düsseldorf, 40225 Düsseldorf, Germany

3. Institute of Chemical Biology and Fundamental Medicine SB RAS, 630090 Novosibirsk, Russia

4. Laboratoire de Chimie de Coordination, CNRS, 205 Route de Narbonne, CEDEX 04, 31077 Toulouse, France

5. Molecular and Experimental Surgery, Clinic for General-, Visceral-, Vascular-, and Transplant-Surgery, Medical Faculty, University Hospital Magdeburg, 39120 Magdeburg, Germany

6. Univ. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, 33600 Pessac, France

Abstract

Glioblastoma is a rapidly progressing tumor quite resistant to conventional treatment. These features are currently assigned to a self-sustaining population of glioblastoma stem cells. Anti-tumor stem cell therapy calls for a new means of treatment. In particular, microRNA-based treatment is a solution, which in turn requires specific carriers for intracellular delivery of functional oligonucleotides. Herein, we report a preclinical in vitro validation of antitumor activity of nanoformulations containing antitumor microRNA miR-34a and microRNA-21 synthetic inhibitor and polycationic phosphorus and carbosilane dendrimers. The testing was carried out in a panel of glioblastoma and glioma cell lines, glioblastoma stem-like cells and induced pluripotent stem cells. We have shown dendrimer-microRNA nanoformulations to induce cell death in a controllable manner, with cytotoxic effects being more pronounced in tumor cells than in non-tumor stem cells. Furthermore, nanoformulations affected the expression of proteins responsible for interactions between the tumor and its immune microenvironment: surface markers (PD-L1, TIM3, CD47) and IL-10. Our findings evidence the potential of dendrimer-based therapeutic constructions for the anti-tumor stem cell therapy worth further investigation.

Funder

COST

Heinrich-Heine University Düsseldorf, Germany within the STIBET programme

CNRS

Publisher

MDPI AG

Subject

Pharmaceutical Science

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