GNS_CELLS

Biochemical and functional studies of lineage-specific transcription factor complexes in glioblastoma-derived stem cells

 Coordinatore UNIVERSITY COLLEGE LONDON 

 Organization address address: GOWER STREET
city: LONDON
postcode: WC1E 6BT

contact info
Titolo: Ms.
Nome: Greta
Cognome: Borg-Carbot
Email: send email
Telefono: 442031000000
Fax: 442078000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 200˙049 €
 EC contributo 200˙049 €
 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-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-06-01   -   2013-05-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE LONDON

 Organization address address: GOWER STREET
city: LONDON
postcode: WC1E 6BT

contact info
Titolo: Ms.
Nome: Greta
Cognome: Borg-Carbot
Email: send email
Telefono: 442031000000
Fax: 442078000000

UK (LONDON) coordinator 200˙049.60

Mappa


 Word cloud

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

gbm    stem    cancers    differentiation    cell    operate    pathways    cancer    cells    progenitor    proliferation    disease    developmental    biology   

 Obiettivo del progetto (Objective)

'Cancer is one of the leading causes of death worldwide. Brain cancers, in particular glioblastoma (GBM), have incredibly poor prognosis and there are currently few effective treatments. Our understanding of the molecular defects associated with cancer has significantly increased over the past decade. Many of the commonly disrupted genes control cell proliferation and survival pathways. However, it is increasingly clear that genetic changes operate in a tissue-specific and developmental context and cancer can be viewed as a disease of aberrant cell differentiation. For some cancers, including GBM, cells with stem cell characteristics may initiate and/or sustain tumour growth. Therefore, knowledge and methods from developmental biology and stem cell biology are likely to provide new insights into the biology of this disease and lead to new therapeutic strategies.

I will focus on a set of lineage-specific transcription factors with known expression within neural stem and progenitor cells, both in vitro and in vivo. My goal is to dissect their role in self-renewal and differentiation and how this is related to the cell cycle machinery and “classic” cancer pathways. How cell differentiation and cell proliferation programs operate in stem and progenitor cells is a fundamental question for both basic biology and cancer research.'

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