A Novel Patient‐Personalized Nanovector Based on Homotypic Recognition and Magnetic Hyperthermia for an Efficient Treatment of Glioblastoma Multiforme

Author:

De Pasquale Daniele1,Pucci Carlotta1,Desii Andrea1,Marino Attilio1,Debellis Doriana2,Leoncino Luca2,Prato Mirko3,Moscato Stefania4,Amadio Simone1,Fiaschi Pietro56,Prior Alessandro5,Ciofani Gianni1ORCID

Affiliation:

1. Smart Bio‐Interfaces Istituto Italiano di Tecnologia Viale Rinaldo Piaggio 34 56025 Pontedera Italy

2. Electron Microscopy Facility Istituto Italiano di Tecnologia Via Morego 30 16163 Genova Italy

3. Materials Characterization Facility Istituto Italiano di Tecnologia Via Morego 30 16163 Genova Italy

4. Department of Clinical and Experimental Medicine University of Pisa Via Roma 55 56126 Pisa Italy

5. Department of Neurosurgery IRCCS Ospedale Policlinico San Martino Largo Rossana Benzi 10 16132 Genova Italy

6. Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI) University of Genova Largo Paolo Daneo 3 16132 Genova Italy

Abstract

AbstractGlioblastoma multiforme (GBM) is the deadliest brain tumor, characterized by an extreme genotypic and phenotypic variability, besides a high infiltrative nature in healthy tissues. Apart from very invasive surgical procedures, to date, there are no effective treatments, and life expectancy is very limited. In this work, an innovative therapeutic approach based on lipid‐based magnetic nanovectors is proposed, owning a dual therapeutic function: chemotherapy, thanks to an antineoplastic drug (regorafenib) loaded in the core, and localized magnetic hyperthermia, thanks to the presence of iron oxide nanoparticles, remotely activated by an alternating magnetic field. The drug is selected based on ad hoc patient‐specific screenings; moreover, the nanovector is decorated with cell membranes derived from patients’ cells, aiming at increasing homotypic and personalized targeting. It is demonstrated that this functionalization not only enhances the selectivity of the nanovectors toward patient‐derived GBM cells, but also their blood–brain barrier in vitro crossing ability. The localized magnetic hyperthermia induces both thermal and oxidative intracellular stress that lead to lysosomal membrane permeabilization and to the release of proteolytic enzymes into the cytosol. Collected results show that hyperthermia and chemotherapy work in synergy to reduce GBM cell invasion properties, to induce intracellular damage and, eventually, to prompt cellular death.

Funder

Associazione Italiana per la Ricerca sul Cancro

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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