Glioblastoma multiforme (GBM) is an extremely aggressive type of glioma. Life expectancy is around two years after diagnosis, due to recidivism and to the presence of the blood brain barrier (BBB) restricting the amount of drugs which arrive at the residual cancer cells, thus contributing to chemotherapies failure. To overcome the impediment imposed by the BBB, we have investigated the use of nanotechnologies in synergy with radiotherapy as a prospective strategy for GBM treatment. We have used poly(lactic-co-glycolic acid) (PLGA) nanoparticles (PNP) conjugated to the peptide chlorotoxin (CTX), which has been shown to recognize and selectively bind to glioma cells. Silver nanoparticles have been encapsulated inside the functionalized nanoparticles (Ag-PNP-CTX), to allow detection of cellular uptake and quantification by means of confocal microscopy, both in vitro and in vivo. In vitro experiments, involving 3 different human glioblastoma cell lines, have shown that the cytoplasmic uptake of Ag-PNP-CTX is higher than that of non-functionalized nanoparticles. Experiments performed in vivo have shown high efficiency of Ag-NP-CTX particles in targeting tumor cells; however, they have been shown to be scarcely able to cross the blood brain barrier at the healthy brain level, where scattered metastatic cells are present too. A single x-rays administration on the whole brain, carried out twenty hours before the injection of the nanoparticles, has been shown to increase the levels of expression of the CTX targets MMP-2 e ClC-3. Moreover, through an alteration of BBB permeability, it has been shown to potentially increase the quantity of internalized Ag-PNP-CTX also in dispersed cells, and to lead to significant results in inhibiting tumor growth in vivo. Notably, the administration of Ag-PNP-CTX to irradiated tumor cells decreases the MMP-2 extracellular activity. By targeting scattered GBM cells and limiting MMP-2 activity, the synergic use of nanovectors conjugated with CTX and radiotherapy may represent an efficient therapeutic approach to GBM treatment.

A NANOTECHNOLOGY APPROACH FOR GLIOBLASTOMA TARGETED THERAPY / M. Tamborini ; tutor: A. Panerai ; co-tutor: C. Gotti ; directeur of studies: A. Corsini. - : . DIPARTIMENTO DI BIOTECNOLOGIE MEDICHE E MEDICINA TRASLAZIONALE, 2016 Jan 11. ((28. ciclo, Anno Accademico 2015. [10.13130/m-tamborini_phd2016-01-11].

A NANOTECHNOLOGY APPROACH FOR GLIOBLASTOMA TARGETED THERAPY

M. Tamborini
2016-01-11

Abstract

Glioblastoma multiforme (GBM) is an extremely aggressive type of glioma. Life expectancy is around two years after diagnosis, due to recidivism and to the presence of the blood brain barrier (BBB) restricting the amount of drugs which arrive at the residual cancer cells, thus contributing to chemotherapies failure. To overcome the impediment imposed by the BBB, we have investigated the use of nanotechnologies in synergy with radiotherapy as a prospective strategy for GBM treatment. We have used poly(lactic-co-glycolic acid) (PLGA) nanoparticles (PNP) conjugated to the peptide chlorotoxin (CTX), which has been shown to recognize and selectively bind to glioma cells. Silver nanoparticles have been encapsulated inside the functionalized nanoparticles (Ag-PNP-CTX), to allow detection of cellular uptake and quantification by means of confocal microscopy, both in vitro and in vivo. In vitro experiments, involving 3 different human glioblastoma cell lines, have shown that the cytoplasmic uptake of Ag-PNP-CTX is higher than that of non-functionalized nanoparticles. Experiments performed in vivo have shown high efficiency of Ag-NP-CTX particles in targeting tumor cells; however, they have been shown to be scarcely able to cross the blood brain barrier at the healthy brain level, where scattered metastatic cells are present too. A single x-rays administration on the whole brain, carried out twenty hours before the injection of the nanoparticles, has been shown to increase the levels of expression of the CTX targets MMP-2 e ClC-3. Moreover, through an alteration of BBB permeability, it has been shown to potentially increase the quantity of internalized Ag-PNP-CTX also in dispersed cells, and to lead to significant results in inhibiting tumor growth in vivo. Notably, the administration of Ag-PNP-CTX to irradiated tumor cells decreases the MMP-2 extracellular activity. By targeting scattered GBM cells and limiting MMP-2 activity, the synergic use of nanovectors conjugated with CTX and radiotherapy may represent an efficient therapeutic approach to GBM treatment.
PANERAI, ALBERTO EMILIO
CORSINI, ALBERTO
Settore BIO/14 - Farmacologia
A NANOTECHNOLOGY APPROACH FOR GLIOBLASTOMA TARGETED THERAPY / M. Tamborini ; tutor: A. Panerai ; co-tutor: C. Gotti ; directeur of studies: A. Corsini. - : . DIPARTIMENTO DI BIOTECNOLOGIE MEDICHE E MEDICINA TRASLAZIONALE, 2016 Jan 11. ((28. ciclo, Anno Accademico 2015. [10.13130/m-tamborini_phd2016-01-11].
Doctoral Thesis
File in questo prodotto:
File Dimensione Formato  
phd_unimi_R10181.pdf

embargo fino al 31/12/2016

Tipologia: Tesi di dottorato completa
Dimensione 1.96 MB
Formato Adobe PDF
1.96 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

Caricamento pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/351946
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact