BIOMAG

Magnetic Biomaterials: Magnetically Loaded Stem Cells as Diagnostic and Therapeutic Vectors for Lung Cancer

 Coordinatore The Royal Institution of Great Britain 

 Organization address address: Albemarle Street 21
city: London
postcode: W15 4BS

contact info
Titolo: Prof.
Nome: Quentin Andrew
Cognome: Pankhurst
Email: send email
Telefono: 44 7962 232 340
Fax: 44 20 7670 2920

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 0 €
 EC contributo 181˙350 €
 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-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-05-01   -   2011-04-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    The Royal Institution of Great Britain

 Organization address address: Albemarle Street 21
city: London
postcode: W15 4BS

contact info
Titolo: Prof.
Nome: Quentin Andrew
Cognome: Pankhurst
Email: send email
Telefono: 44 7962 232 340
Fax: 44 20 7670 2920

UK (London) coordinator 181˙350.77

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

lung    sensing    disease    bio    tumour    mscs    msc    nanoparticles    engraftment    cancer    patients    compatible    heating    mri    magnetic    treating   

 Obiettivo del progetto (Objective)

'Lung cancer is the most lethal cancer in the world today. There are limited options for clinicians when treating patients, with only 10-15% of lung cancer patients surviving their malignancy. Despite the introduction of new chemotherapies, lung cancer survival is unchanged from thirty years ago. New ways of treating this disease are needed. We hypothesise that modified mesenchymal stem cells (MSCs) may be used to deliver magnetic nanoparticles through their engraftment, killing both tumour epithelium and tumour vasculature, while preserving normal tissue. We propose to introduce bio-compatible tailored magnetic nanoparticles into the MSCs to enable localised cellular-level sensing and heating while retaining the full viability and functionality of the MSCs. We will examine the kinetics of MSC engraftment and compare histological samples to in vivo quantification of engraftment using contrast-enhanced small animal magnetic resonance imaging (MRI) based on sensing the MRI signal of the introduced nanoparticles. MSCs will subsequently be locally heated by applying a time-varying electromagnetic field to induce heating of the nanoparticles (a process similar in principle to that used in microwave ovens) and consequent tumour destruction. MSC delivered therapy is particularly attractive. MSCs are easy to culture, expand and genetically manipulate. They are immuno-privileged, and also home preferentially to tumour tissues allowing systemic delivery to widespread tumour and metastases. As such they offer a uniquely bio-compatible, patient-derived therapeutic solution to the life-threatening disease of lung cancer.'

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