PEDIAVIR

New Therapeutics Strategies for the Treatment of Pediatric Brain Tumors

 Coordinatore UNIVERSIDAD DE NAVARRA 

 Organization address address: CAMPUS UNIVERSITARIO EDIFICIO CENTRAL
city: PAMPLONA
postcode: 31080

contact info
Titolo: Dr.
Nome: Iñigo
Cognome: Uriarte-Pueyo
Email: send email
Telefono: +34 948 176 748
Fax: +34 948 175 223

 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

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSIDAD DE NAVARRA

 Organization address address: CAMPUS UNIVERSITARIO EDIFICIO CENTRAL
city: PAMPLONA
postcode: 31080

contact info
Titolo: Dr.
Nome: Iñigo
Cognome: Uriarte-Pueyo
Email: send email
Telefono: +34 948 176 748
Fax: +34 948 175 223

ES (PAMPLONA) coordinator 100˙000.00

Mappa


 Word cloud

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

brain    improvement    treatment    adenovirus    rgd    btscs    chemotherapy    population    pediatric    oncolytic    delta    children    tumor    malignancies    life    resistance    cells    constitute    effect    therapeutic    cancer    radiotherapy    prognosis    quality    tumors    significant    combination   

 Obiettivo del progetto (Objective)

'High-risk pediatric brain tumors constitute the leading cause of cancer death in children and despite the improvement of diagnostic and therapeutic approaches children with these malignancies have a very poor prognosis. Thus, it is clear that the management of these malignancies is suboptimal and novel targeted therapeutic strategies are required. Recently, a cancer stem cell population has been found responsible for the initiation of adult and pediatric brain tumors and may constitute the cellular basis for the resistance of these tumors to chemotherapy and radiotherapy and a more reliable model to study these malignancies. One of the approaches used to design novel, rational, and effective treatments directed against the molecular defects of these tumors involves the use of oncolytic adenoviruses. Our group previously reported the anti-glioma effect of the tumor-selective adenovirus, Delta-24-RGD engineered to selectively replicate in cells that harbor an abnormal RB pathway, a hallmark of cancer. We hypothesize that a targeted oncolytic adenovirus design to target not only the bulk of the tumor but also the BTSCs population, which account for resistance and recurrence, may constitute a significant improvement of the prognosis and quality of life of patient with pediatric brain tumors. Since the percentage of BTSCs would vary along the different pediatric brain tumors this strategy will be likely to be used in combinations, to maximize clinical impact and to minimize opportunities for resistant cancer cells to emerge. Consequently, we shall evaluate the cytotoxic effect of Delta-24-RGD in combination with temozolomide. Importantly, Delta-24-RGD in combination with chemotherapy would avoid the use of radiotherapy which, in turn, will prevent the subsequent loss of cognitive function without compromising disease control and thus, improving the overall quality of life for these children.'

Introduzione (Teaser)

A new therapy based on oncolytic viruses is being tested for the treatment of paediatric gliomas. Used in combination with chemotherapy, this novel approach holds significant hope for a more effective treatment of this malignancy.

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