SYNTHLE BRCA

Synthetic lethality approaches to BRCA-associated cancer

 Coordinatore INSTITUTE OF CANCER RESEARCH - ROYAL CANCER HOSPITAL 

 Organization address address: Old Brompton Road 123
city: LONDON
postcode: SW7 3RP

contact info
Titolo: Ms.
Nome: Binoo
Cognome: Rastogi
Email: send email
Telefono: +44 (0) 20 7153 5196
Fax: +44 (0) 20 7153 5534

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 169˙390 €
 EC contributo 169˙390 €
 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-2007-2-1-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-09-01   -   2010-08-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUTE OF CANCER RESEARCH - ROYAL CANCER HOSPITAL

 Organization address address: Old Brompton Road 123
city: LONDON
postcode: SW7 3RP

contact info
Titolo: Ms.
Nome: Binoo
Cognome: Rastogi
Email: send email
Telefono: +44 (0) 20 7153 5196
Fax: +44 (0) 20 7153 5534

UK (LONDON) coordinator 0.00

Mappa


 Word cloud

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

rnai    breast    synthetic    brca    cancers    lethality    cells    repair    dna    defects    proteins   

 Obiettivo del progetto (Objective)

'Mutations in BRCA1 and BRCA2 genes confer high lifetime risks of developing breast and other cancers. Moreover, several studies suggest that tumours arising in mutation carriers have generally lost the wild-type allele and do not express functional BRCA1 or BRCA2 proteins. Both BRCA proteins are important for repair of double strand DNA breaks by homologous recombination. The subject of this project would allow us to clarify if cells harbouring defects in DNA damage repair (such as BRCA1 deficient cells) are more sensitive to the induced loss of other DNA repair mechanisms (either by RNAi or small molecule inhibitors). For that purpose I will perform High-throughput RNA interference screenings to find synthetic lethality partners for BRCA1 and BRCA2, using a library of siRNAs targeting 779 proteins that encompass all the known and predicted kinases. I will also translate some previous yeast synthetic lethality studies, to human breast cancer cell lines, performing for that a”mini-RNAi screen”. Ultimately, this project presented here may lead to the identification of novel anticancer strategies targeting DNA repair defects in tumors, which could be applicable in several sporadic cancers.'

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