Coordinatore | FUNDACIO SANT JOAN DE DEU
Organization address
address: Calle Santa Rosa contact info |
Nazionalità Coordinatore | Spain [ES] |
Totale costo | 100˙000 € |
EC contributo | 100˙000 € |
Programma | FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
Code Call | FP7-PEOPLE-2010-RG |
Funding Scheme | MC-IRG |
Anno di inizio | 2011 |
Periodo (anno-mese-giorno) | 2011-04-01 - 2015-03-31 |
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1 |
FUNDACIO SANT JOAN DE DEU
Organization address
address: Calle Santa Rosa contact info |
ES (Esplugues de Ll) | coordinator | 100˙000.00 |
Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.
'Background/Main objective: Neuroblastoma, a solid tumor of the childhood, is the cause of 15% of deaths by cancer in children under the age of 15. Survival of advanced stage neuroblastoma patients remains poor (around 30%), because these tumors rapidly develop resistance to conventional treatments. The poor penetration of chemotherapy agents to the target tumor cells is considered one of the main mechanisms of drug resistance in solid malignancies. Therefore, the main objective of this project is to design pharmacological treatments that circumvent some of the resistance mechanisms and penetrate more efficiently to the neuroblastoma tumor cells. Methodology: We hypothesize that the penetration and activity of the genotoxic drug SN-38 in neuroblastoma tumor xenografts will be improved by its formulation as micelles and by the administration of concomitant nutlin and vandetanib (two new drugs with remarkable anti-neuroblastoma effect). To address this hypothesis, we will prepare SN-38 micelles by the self-assembly of amphiphilic polymers in water. To evaluate the penetration of SN-38 micelles to neuroblastoma xenografts, we will apply a microdialysis technique to sample the extracellular fluid of the tumors and we will analyze drug concentrations in the dialyzates. We will evaluate the effect of nutlin and vandetanib on the tumor penetration and activity of SN-38. Finally, we will test the efficacy of our treatments in a neuroblastoma tumor model and will correlate drug concentrations in plasma and tumor with the observed antineoplastic activity. Expected results: We will identify more effective therapies than the currently available for the treatment of neuroblastoma. We expect that our research will be able to rapidly be translated to the clinic and help rationally design clinical trials for the multidrug resistant neuroblastoma.'
During conventional chemotherapy, a neuroblastoma tumour rapidly develops drug resistance. The goal of an EU-funded project is to design novel pharmacological formulation for better drug delivery.
Neuroblastoma is a solid neuroendocrine tumour presenting in childhood and infancy. It is the cause of 15 % of deaths by cancer in children under the age of 15. Survival of neuroblastoma patients remains poor (around 30 %) because these tumours rapidly develop resistance to conventional treatments. The poor penetration of chemotherapy agents to the targeted tumour cells is the main mechanism of drug resistance in solid malignancies.
The main goal of the EU-funded 'Chemotherapy of neuroblastoma' (NEUROBLASTOMA CHEMO) project is to design pharmacological treatments that circumvent some of the resistance mechanisms and more efficiently penetrate the neuroblastoma tumour cells. Over the first 24 months of the project, researchers established 7 new neuroblastoma mouse xenograft models from the patients. They developed a micro-dialysis method to sample a model small-molecule drug in the tumour extracellular fluid of the animals.
Studies of the penetration of the anti-cancer agents in xenografts of highly aggressive and chemo-resistant neuroblastomas are currently underway. In the next stage of the project, researchers will test the development of improved drug delivery using micromicelles formulation.
Project members are collecting data to evaluate the role of limited drug distribution on neuroblastoma chemoresistance. Such data will enable the design of strategies to overcome tumour drug resistance barriers and optimise anti-cancer therapy.
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